Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
A new insight into viral proteins as Immunomodulatory therapeutic agents. KSHV vOX2 a homolog of human CD200 as a potent anti-inflammatory protein
2
13
EN
Maryam
Mousavinezhad-Moghaddam
Department of Physiology, Biology Division, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran
Abbas Ali
Amin
Department of Immunology, Faculty of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran
Houshang
Rafatpanah
Immunology Research Centre, Bu-Ali Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran
hrafatpanah@hotmail.com
Seyed Abdol
Rahim Rezaee
Inflammation and Inflammatory Diseases Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
rezaeer@mums
10.22038/ijbms.2016.6408
The physiologic function of the immune system is defense against infectious microbes and internal tumour cells, Therefore, need to have precise modulatory mechanisms to maintain the body homeostasis. The mammalian cellular CD200 (OX2)/CD200R interaction is one of such modulatory mechanisms in which myeloid and lymphoid cells are regulated. CD200 and CD200R molecules are membrane proteins that their immunomodulatory effects are able to suppress inflammatory responses, particularly in the privilege sites such as CNS and eyes. Kaposi’s sarcoma-associated herpesvirus (KSHV), encodes a wide variety of immunoregulatory proteins which play central roles in modulating inflammatory and anti-inflammatory responses in favour of virus dissemination. One such protein is a homologue of the, encoded by open reading frame (ORF) K14 and therefore called vOX2. Based on its gene expression profile during the KSHV life cycle, it is hypothesised that vOX2 modulates host inflammatory responses. Moreover, it seems that vOX2 involves in cell adhesion and modulates innate immunity and promotes Th2 immune responses. In this review the activities of mammalian CD200 and KSHV CD200 in cell adhesion and immune system modulation are reviewed in the context of potential therapeutic agents.
CD200,Immune modulation,KSHV,RGD,vCD200,vOX2
https://ijbms.mums.ac.ir/article_6408.html
https://ijbms.mums.ac.ir/article_6408_620ebdfdfb45f513ce17002304ff0b9c.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Chemically primed bone-marrow derived mesenchymal stem cells show enhanced expression of chemokine receptors contributed to their migration capability
14
19
EN
Hamid Reza
Bidkhori
0000-0002-0204-0351
Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran
hbidkhori@gmail.com
Naghmeh
Ahmadiankia
Shahroud University of Medical Sciences, Shahroud, Iran
f.kalalian@gmail.com
Maryam
Moghaddam Matin
0000-0002-7949-7712
Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran
matin@um.ac.ir
Asieh
Heirani tabasi
Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran
Moein
Farshchian
0000-0002-1228-048X
Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran
moeinfarshchy@yahoo.com
Hojjat
Naderi-meshkin
0000-0003-3988-3229
Stem Cells and Regenerative Medicine Research Department, ACECR-Khorasan Razavi Branch, Mashhad, Iran
nahojjat@gmail.com
Mina
Shahriyari
Stem Cells and Regenerative Medicine Research Department, ACECR-Khorasan Razavi Branch, Mashhad, Iran
m.shahriyari@outlook.com
Mahtab
Dastpak
Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran
ma.dastpak@gmail.com
Ahmad Reza
Bahrami
Department of Biology, Faculty of Sciences, Ferdowsi University of Mashhad, Mashhad, Iran
ar-bahram@um.ac.ir
10.22038/ijbms.2016.6409
<strong><em>Objective(s):</em></strong>The limited homing potential of bone-marrow-derived mesenchymal stem cells (BM-MSC) is the key obstacle in MSC-based therapy. It is believed that chemokines and chemokine receptor interactions play key roles in cellular processes associated with migration. Meanwhile, MSCs express a low level of distinct chemokine receptors and they even lose these receptors on their surface after a few passages which influence their therapeutic applications negatively. This study investigated whether treatment of BM-MSCs with hypoxia-mimicking agents would increase expression of some chemokine receptors and cell migration. <br/><strong><em>Materials and Methods:</em></strong> BM-MSCs were treated at passage 2 for our gene expression profiling. All qPCR experiments were performed by SYBR Green method in CFX-96 Bio-Rad Real-Time PCR. The Boyden chamber assay was utilized to investigate BM-MSC homing. <br/><strong><em>Results:</em></strong>Possible approaches to increasing the expression level of chemokine receptors by different hypoxia-mimicking agents such as valproic acid (VPA), CoCl<sub>2,</sub> and desferrioxamine (DFX) are described. Results show DFX efficiently up-regulate the <em>CXCR7</em> and <em>CXCR4</em> gene expression while VPA increase only the <em>CXCR7</em> gene expression and no significant change in expression level of <em>CXCR4</em> and the <em>CXCR7</em> gene was detectable by CoCl<sub>2</sub> treatment. Chemotaxis assay results show that pre-treatment with DFX, VPA, and Cocl<sub>2</sub> enhances significantly the migration ability of BM-MSCs compared with the untreated control group and DFX treatment accelerates MSCs homing significantly with a higher rate than VPA and Cocl<sub>2 </sub>treatments<sub>.</sub> <br/><strong><em>Conclusion</em></strong><strong>: </strong>Our data supports the notion that pretreatment of MSC with VPA and DFX improves the efficiency of MSC therapy by triggering homing regulatory signaling pathways.
CXCR4,CXCR7,CoCl2,Desferrioxamine,MSC,Chemical treatment,Homing,Valproic acid
https://ijbms.mums.ac.ir/article_6409.html
https://ijbms.mums.ac.ir/article_6409_eace9d6f07c7fd009845ce6e5b4fe7ab.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Conjugated linoleic acid supplementation enhances insulin sensitivity and peroxisome proliferator-activated receptor gamma and glucose transporter type 4 protein expression in the skeletal muscles of rats during endurance exercise
20
27
EN
Kangok
Cho
Institute of Sports Health Science, Sunmoon University, Asan city, Chung Nam, 380-701, S. Korea
okcho1@snu.ac.kr
Youngju
Song
Institute of Sports Health Science, Sunmoon University, Asan city, Chung Nam, 380-701, S. Korea
song6711@sunmoon.ac.kr
Daekeun
Kwon
Institute of Sports Health Science, Sunmoon University, Asan city, Chung Nam, 380-701, S. Korea
ksunsu@hanmail.net
10.22038/ijbms.2016.6410
<strong><em>Objective(s)</em><em>:</em></strong>This study examined whether conjugated linoleic acid (CLA) supplementation affects insulin sensitivity and peroxisome proliferator-activated receptor gamma (PPAR-γ) and glucose transporter type 4 (GLUT-4) protein expressions in the skeletal muscles of rats during endurance exercise.
<strong><em>Materials and Methods</em><em>:</em></strong>Sprague-Dawley male rats were randomly divided into HS (high-fat diet (HFD) sedentary group, n = 8), CS (1.0% CLA supplemented HFD sedentary group, n = 8), and CE (1.0% CLA supplemented HFD exercise group, n = 8). The rats in the CE swam for 60 min a day, 5 days a week for 8 weeks.
<strong><em>Results:</em></strong>The serum glucose and insulin contents and homeostasis model assessment of insulin resistance (HOMA-IR) value of the CS and CE were significantly decreased compared to those of the HS. The PPAR-γ protein expressions in the soleus muscle (SOM) and extensor digitorum longus muscle (EDL) were significantly higher in the CE than in the HS. In addition, the PPAR-γ protein expression in the SOM of the CS was significantly higher than that in the HS. On the other hand, the GLUT-4 protein expression of the SOM in the CE was significantly higher compared to that in the HS. However, there was no significant difference in GLUT-4 protein expression in the EDL among the groups.
<strong><em>Conclusion:</em></strong>CLA supplementation with/without endurance exercise has role in improvement of insulin sensitivity. Moreover, when CLA supplementation was accompanied by endurance exercise, the PPAR-γ protein expression in SOM and EDL and the GLUT-4 protein expression in SOM were enhanced compared with the control group.
Conjugated linoleic acid,Endurance exercise Insulin,PPAR-γ,GLUT-4
https://ijbms.mums.ac.ir/article_6410.html
https://ijbms.mums.ac.ir/article_6410_bd8e4b0401a56b04adcabd076b789028.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Inactivation of mitogen-activated protein kinase signaling pathway reduces caspase-14 expression in impaired keratinocytes
28
33
EN
Ningning
Dang
Department of Dermatology, Jinan Central Hospital affiliated to Shandong University, Jinan, Shandong Province, 250013, China
15318816250@163.com
Shuguang
Pang
Department of Endocrinology, Jinan Central Hospital affiliated to Shandong University, Jinan, Shandong Province, 250013, China
Haiyan
Song
Department of Dermatology, Jinan Central Hospital affiliated to Shandong University, Jinan, Shandong Province, 250013, China
Liguo
An
College of Life Science, Shandong Normal University, Jinan Shandong Province, 250014, China
Xiaoli
Ma
Central Laboratory, Jinan Central Hospital affiliated to Shandong University, Jinan, Shandong Province, 250013, China
maxl7125@yahoo.com
10.22038/ijbms.2016.6411
<strong><em>Objective(s):</em></strong>Several investigations have revealed that caspase-14 is responsible for the epidermal differentiation and cornification, as well as the regulation of moisturizing effect. However, the precise regulation mechanism is still not clear. This study was aimed to investigate the expression of caspase-14 in filaggrin-deficient normal human epidermal keratinocytes (NHEKs) and to explore the possible mechanism that contributes to the regulation of caspase-14. <br/><strong><em>Materials and Methods:</em></strong>The filaggrin-deficient NHEKs were induced by transfection with lentivirus (LV) vector encoding small hairpin RNAs (shRNA). The inhibitors SB203580, PD98059 and SP600125 were used for suppressing the expression of p38 mitogen-activated protein kinase (MAPK), p44/42 MAPK and stress-activated protein kinase/c-Jun N-terminal kinase (SAPK/JNK). The expression of filaggrin, p38 MAPK, p44/42 MAPK and SAPK/JNK, caspase-14, keratin1and keratin2 were detected by western blot. <br/><strong><em>Results:</em></strong>In filaggrin-deficient NHEKs, the expression of p38, p44/42 MAPK and SAPK/JNK and caspase-14 were significantly decreased. The inhibition of p38 and SAPK/JNK reduced the expression of caspase-14, while the p44/42 MAPK showed no consistent effects. Moreover, the filaggrin knockdown decreased the expression of keratin2, but had no effects on the level of keratin1. <br/><strong><em>Conclusion</em></strong><strong><em>: </em></strong>The decreased expression of caspase-14 in filaggrin-deficient NHEKs may be induced by the inactivation of MAPK signaling pathway. These provide a novel perspective to understand the mechanism for the protective effects of filaggrin and caspase-14 on skin barrier function.
Caspase-14,Filaggrin,MAPK signaling pathway Skin barrier
https://ijbms.mums.ac.ir/article_6411.html
https://ijbms.mums.ac.ir/article_6411_b409eb9e7086c3724b66c2cb8c669cb6.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Laminin matrix promotes hepatogenic terminal differentiation of human bone marrow mesenchymal stem cells
34
42
EN
Zahra
Khalaj
Animal and Marine Biotechnology Department, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran
Abbas
Sahebghadam Lotfi
0000-0003-3256-3943
Animal and Marine Biotechnology Department, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran
lotfi_ab@modares.ac.ir
Maryam
Kabir-Salmani
Biomaterials and Tissue Engineering Department, Stem Cell Division, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran
10.22038/ijbms.2016.6412
<strong><em>Objective(s)</em><em>:</em></strong>The application of stem cells holds great promises in cell transplants. Considering the lack of optimal <em>in vitro</em> model for hepatogenic differentiation, this study was designed to examine the effects of laminin matrix on the improvement of <em>in vitro</em> differentiation of human bone marrow mesenchymal stem cells (hBM-MSC) into the more functional hepatocyte-like cells.
<strong><em>Materials and Methods</em><em>:</em></strong>Characterization of the hBM-MSCs was performed by immunophenotyping and their differentiation into the mesenchymal-derived lineage. Then, cells were seeded on the laminin-coated or tissue culture polystyrene (TCPS). The differentiation was carried out during two steps. Afterward, the expression of hepatocyte markers such as AFP, ALB, CK-18, and CK-19 as well as the expression of C-MET, the secretion of urea, and the activity of CYP3A4 enzyme were determined. Moreover, the cytoplasmic glycogen storage was examined by periodic acid–Schiff (PAS) staining.
<strong><em>Results:</em></strong>The results demonstrated that the culture of hBM-MSC on laminin considerably improved hepatogenic differentiation compared to TCP group. A significant elevated level of urea biosynthesis and CYP3A4 enzyme activity was observed in the media of the laminin-coated differentiated cells (<em>P</em><0.05). Furthermore higher expressions of both AFP and ALB were determined in cells differentiated on laminin matrix. Glycogen accumulation was not detected in the undifferentiated hBM-MSCs, however, both differentiated cells in laminin and TCPS groups demonstrated the intracellular glycogen accumulation on day 21 of hepatogenic differentiation.
<strong><em>Conclusion:</em></strong>Taken together, these findings may indicate that laminin matrix can improve terminal differentiation of hepatocyte-like cells from hBM-MSCs. Thus, laminin might be considered as a suitable coating in hepatic tissue engineering designs.
bone marrow,Differentiation,Hepatocyte,Laminin,Mesenchymal stem cell
https://ijbms.mums.ac.ir/article_6412.html
https://ijbms.mums.ac.ir/article_6412_1a1645fd8d0d8126bd09b31990d9e71e.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Application of citrate as a tricarboxylic acid (TCA) cycle intermediate, prevents diabetic-induced heart damages in mice
43
48
EN
Qianqian
Liang
Department of Emergency, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, 450007China
Baoyu
Wang
Department of Emergency, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, 450007China
baoyuwang12@163.com
Lingxia
Pang
Function Experiment Teaching Center, Wenzhou Medical University, Wenzhou, 325305China
lingxiapang@163.com
Youpei
Wang
Function Experiment Teaching Center, Wenzhou Medical University, Wenzhou, 325305China
wangyoupei@163.com
Meiqin
Zheng
The Affiliated Eye Hospital, Wenzhou Medical University, Wenzhou, 325000China
mqzheng1973@163.com
Qing
Wang
The Affiliated Eye Hospital, Wenzhou Medical University, Wenzhou, 325000China
denniswq@yahoo.com
Jingbin
Yan
Department of Pain management, Wenzhou Hospital of integrated Chinese and Western Medicine, Wenzhou, 325000 China
13758483130@163.com
Jinzhong
Xu
Wenling First People’s Hospital, The Affiliated Hospital of Wenzhou Medical University, Wenling, 317500
fengzhongjin@163.com
10.22038/ijbms.2016.6413
<strong><em>Objective(s):</em></strong>Higher cellular reactive oxygen species (ROS) levels is important in reducing cellular energy charge (EC) by increasing the levels of key metabolic protein, and nitrosative modifications, and have been shown to damage the cardiac tissue of diabetic mice. However, the relation between energy production and heart function is unclear.
<strong><em>Materials and Methods:</em></strong>Streptozotocin (STZ, 150 mg/kg body weight) was injected intraperitoneally once to mice that had been fasted overnight for induction of diabetes. After diabetic induction, mice received citrate (5 µg/kg) through intraperitoneal injection every other day for 5 weeks. The caspase-3, plasminogen activator inhibitor 1 (PAI1), protein kinase B (PKB), commonly known as AKT and phosphorylated-AKT (p-AKT) proteins were examined to elucidate inflammation and apoptosis in the heart. For histological analysis, heart samples were fixed with 10% formalin and stained with hematoxylin-eosin (HE) and Sirius red to assess pathological changes and fibrosis. The expression levels[AGA1] of marker proteins, tyrosine nitration, activity of ATP synthase and succinyl-CoA:3-ketoacid coenzyme A transferase-1 (SCOT), and EC were measured.
<strong><em>Results:</em></strong>Intraperitoneal injection of citrate significantly reduced caspase-3 and PAI-1 protein levels and increased p-AKT level on the 5<sup>th</sup> week; EC in the heart was found to be increased as well. Further, the expression level, activity, and tyrosine nitration of ATP synthase and SCOT were not affected after induction of diabetes.
<strong><em>Conclusion</em></strong><strong><em>: </em></strong>Results indicate that application of citrate, a tricarboxylic acid (TCA) cycle intermediate, might alleviate cardiac dysfunction by reducing cardiac inflammation, apoptosis, and increasing cardiac EC.
Citrate,Diabetes,Heart,Nitration,Tricarboxylic acid
https://ijbms.mums.ac.ir/article_6413.html
https://ijbms.mums.ac.ir/article_6413_43d5122b3c7a1108b74030e4664ec76c.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
The effect of adrenomedullin and proadrenomedullin N- terminal 20 peptide on angiotensin II induced vascular smooth muscle cell proliferation
49
54
EN
Jian
Ma
Cadres Division One, The 401st Hospital of PLA, Qingdao 266071, China
majian4780@163.com
Yinglu
Feng
Cadres Division One, The 401st Hospital of PLA, Qingdao 266071, China
ylfeng1975@yahoo.com.cn
Zaiquan
Li
Institute of Cardiovascular Research, Peking Medical University, First Hospital, Beijing 100083, China
lizaiquan@bjmu.edu.cn
Chaoshu
Tang
Institute of Cardiovascular Research, Peking Medical University, First Hospital, Beijing 100083, China
tangchaoshu@263.net.cn
10.22038/ijbms.2016.6414
<strong><em>Objective(s):</em></strong> The study aimed to investigate the effects of adrenomedullin (ADM) and proadrenomedullin N- terminal 20 peptide (PAMP) on angiotensin II (AngII)-stimulated proliferation in vascular smooth muscle cells (VSMCs).
<strong><em>Materials and Methods:</em></strong> Thoracic aorta was obtained from Wistar rats and VSMCs were isolated from aorta tissues and then cultured. In vitro cultured VSMCs were stimulated with Ang II (10-8 mol/l) followed by various doses of PAMP or ADM (10-9, 10-8, or 10-7 mol/l). Cell proliferation as assessed by 3H-TdR incorporation. Protein kinase C (PKC) activity was measured by counting γ-32P radioactivity with liquid scintillation. In a separate cohort, in vitro cultured rat aortic vessels were treated with different doses of Ang II or PAMP (10-9, 10-8, or 10-7 mol/l). Cellular and secreted levels of PAMP, ADM and Ang II were measured using radioimmunoassay in the tissues and intubation mediums, respectively.
<strong><em>Results: </em></strong>Ang II (10-8 mol/l) treatment significantly increased both 3H-TdR incorporation and PKC activity in VSMCs (by 2.68 and 1.02-fold, respectively; both P<0.01 vs. the control). However, Ang II-induced elevation of 3H-TdR incorporation, and PKC activity was significantly inhibited by various doses of ADM and PAMP (all P<0.01 vs. the Ang II group). In rat aortic vascular tissues or intubation media, Ang II treatments stimulated the expression and secretion of PAMP and ADM in a dose-dependent manner, while PAMP treatments had no significant effects on Ang II levels.
<strong><em>Conclusion:</em></strong> ADM and PAMP inhibit Ang II-induced VSMCs proliferation. The interaction of Ang II, ADM and PAMP may regulate VSMCs and cardiovascular function.
Adrenomedulin,Angiotension II,Proadrenomedullin N-terminal 20 peptide,Proliferation,Vascular smooth muscle- cell
https://ijbms.mums.ac.ir/article_6414.html
https://ijbms.mums.ac.ir/article_6414_1b5275a739e8ef4f1e84488c221c9d6b.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Effect of bone marrow derived mesenchymal stem cells on lung pathology and inflammation in ovalbumin-induced asthma in mouse
55
63
EN
Maryam
Mohammadian
0000-0002-7902-0252
Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
maryam.mohammadian2008@yahoo.com
Mohammad Hosein
Boskabady
Neurogenic Inflammation Research Center and Department of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
Iraj
Ragerdi Kashani
Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
ragerdi@sina.tums.ac.ir
Gila Pirzad
Jahromi
Neuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran
Amene
Omidi
Department of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
omidi_amene@yahoo.com
Amir
Kavian Nejad
Department of Emergency Medical Services, School of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences, Tehran, Iran
amirkaviannejad@yahoo.com
Safoura
Khamse
0000-0002-3833-0289
Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
s.khamseh90@yahoo.com
Hamid Reza
Sadeghipour
0000-0002-7190-8249
Department of Physiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
sadeghipour@tums.ac.ir
10.22038/ijbms.2016.6415
<strong><em>Objective(s)</em><em>:</em></strong>Bone marrow-derived mesenchymal stem cells (BMSCs) have attracted significant interest to treat asthma and its complication. In this study, the effects of BMSCs on lung pathology and inflammation in an ovalbumin-induced asthma model in mouse were examined. <br/><strong><em>Materials and Methods</em><em>:</em></strong>BALB/c mice were divided into three groups: control group (animals were not sensitized), asthma group (animals were sensitized by ovalbumin), asthma+BMSC group (animals were sensitized by ovalbumin and treated with BMSCs). BMSCs were isolated and characterized and then labeled with Bromodeoxyuridine (BrdU). After that the cells transferred into asthmatic mice. Histopathological changes of the airways, BMSCs migration and total and differential white blood cell (WBC) count in bronchoalveolar lavage (BAL) fluid were evaluated. <br/><strong><em>Results:</em></strong>A large number of BrdU-BMSCs were found in the lungs of mice treated with BMSCs. The histopathological changes, BAL total WBC counts and the percentage of neutrophils and eosinophils were increased in asthma group compared to the control group. Treatment with BMSCs significantly decreased airway pathological indices, inflammatory cell infiltration, and also goblet cell hyperplasia. <br/><strong><em>Conclusion:</em></strong>The results of this study revealed that BMSCs therapy significantly suppressed the lung pathology and inflammation in the ovalbumin induced asthma model in mouse.
Inflammation,Lung pathology,Ovalbumin- induced asthma,Stem cells
https://ijbms.mums.ac.ir/article_6415.html
https://ijbms.mums.ac.ir/article_6415_5fdd7524b52de812fd3eacafcd585273.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Lung-derived innate cytokines: new epigenetic targets of allergen-specific sublingual immunotherapy
64
71
EN
Abbas
Pishdadian
School of Medicine, Zabol University of Medical Sciences, Zabol, Iran
pishdadiana891@mums.ac.ir
Abdolreza
Varasteh
Allergy Research Center, Medical School, Mashhad University of Medical Sciences, Mashhad, Iran
Mehran
Gholamin
Division of Human Genetics, Immunology Research Center, Avicenna Research Institute, Mashhad University of Medical Sciences,Mashhad, Iran
golaminm@mums.ac.ir
Leila
Roozbeh Nasiraie
0000000262600103
Department of Food Science, Nour Branch, Islamic Azad University, Nour, Iran
leila_roozbeh@yahoo.com
Mitra
Hosseinpour
Immunology Research Center, Medical School, Mashhad University of Medical Sciences, Mashhad, Iran
hoseinpourm4@mums.ac.ir
Malihe
Moghadam
Immunology Research Center, Medical School, Mashhad University of Medical Sciences, Mashhad, Iran
moghadamm1@mums.ac.ir
Mojtaba
Sankian
Immunology Research Center, Medical School, Mashhad University of Medical Sciences, Mashhad, Iran
sankianm@mums.ac.ir
10.22038/ijbms.2016.6416
<strong><em>Objective(s)</em><em>:</em></strong>Sublingual allergen-specific immunotherapy is a safe and effective method for treatment of IgE-mediated respiratory allergies; however, the underlying mechanisms are not fully understood. This study was planned to test whether sublingual immunotherapy (SLIT) can exert epigenetic mechanisms through which the airway allergic responses can be extinguished. <br/><strong><em>Materials and Methods</em><em>:</em></strong>BALB/c mice were sensitized intraperitoneally and challenged intranasally. Then, they received sublingual treatment with recombinant Che a 2 (rChe a 2), a major allergen of <em>Chenopodium album</em>. After SLIT, allergen-specific antibodies in sera, cytokine profiles of spleen cell cultures, mRNA and protein expression of lung-derived IL-33, IL-25, and TSLP (thymic stromal lymphopoietin), and histone modifications of these three genes were assessed. <br/><em><br/><strong>Results</strong>:</em>Following Immunotherapy, systemic immune responses shifted from Th2 to Th1 profile as demonstrated by significant decrease in IgE and IL-4 and substantial increase in IgG2a and IFN-γ. At local site, mRNA and protein levels of lung-derived pro-inflammatory cytokines IL-33 and TSLP were markedly down-regulated following SLIT that was associated with marked enrichment of trimethylated lysine 27 of histone H3 at promoter regions of these two cytokines. <br/><strong><em>Conclusion:</em></strong>In our study, sublingual immunotherapy with recombinant allergen effectively attenuated allergic immune responses, at least partly, by induction of distinct histone modifications at specific loci. Additionally, the lung-derived pro-allergic cytokines IL-33 and TSLP could be promising mucosal candidates for either monitoring allergic conditions or therapeutic approaches.
Chenopodium album Histone modifications,IL-25,IL-33,Sublingual mmunotherapy,TSLP
https://ijbms.mums.ac.ir/article_6416.html
https://ijbms.mums.ac.ir/article_6416_036caed31e21cd3ee172d87e2e7d1b70.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Protective effects of an interaction between vagus nerve and melatonin on gastric ischemia/reperfusion: the role of oxidative stress
72
79
EN
Nader
Shahrokhi
Physiology Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran
nshahrokhsa@yahoo.com
Mohammad
Khaksari
Endocrinology and Metabolism Research Center, Institute of Basic and Clinical Physiology Sciences, Kerman University of Medical Sciences, Kerman, Iran
m_khaksari@yahoo.com
Shahla
Nourizad
Urmia University of Medical Sciences, Urmia, Iran
Nava Shahrokhi
Shahrokhi
School of Medicine, Kerman University of Medical Sciences, Kerman, Iran
Zahra
Soltani
Gastroenterology and Hepatology Research Center, Institute of Basic and Clinical Physiology Sciences, Dept. of Physiology, Faculty of Medicine, Kerman University of Medical Sciences, Kerman, Iran
Ahmad
Gholamhosseinian
Department of Biochemistry, Medical School of Afzalipour, Kerman University of Medical Sciences, Kerman, Iran
ghol@yahoo.com
10.22038/ijbms.2016.6417
<strong><em>Objectives:</em></strong>Vagal pathways in gastrointestinal tract are the most important pathways that regulate ischemia/reperfusion (I/R). Gastrointestinal tract is one of the important sources of melatonin production. The aim of this study was to investigate probable protective effect of the interaction between vagus nerve and melatonin after I/R. <br/><strong><em>Materials and methods:</em></strong>This study was performed in male rats that were divided into six groups. Cervical vagus nerve was cut bilaterally after induction of I/R and the right one was stimulated by stimulator. Melatonin or vehicle was injected intraperitoneally. The stomach was removed for histopathological and biochemical investigations. <br/><strong><em>Results: </em></strong>A significant decrease in infiltration of gastric neutrophils and malondialdehyde (MDA) level after I/R was induced by melatonin and was disappeared after vagotomy. The stimulation of vagus nerve significantly enhanced these effects of melatonin. However, a stimulation of vagus nerve alone increased neutrophils infiltration and MDA level. Melatonin significantly increased the activities of catalase, glutathione peroxidase (GPx), superoxide dismutases (SOD). Unlike stimulation of vagus nerve, vagotomy decreased these effects of melatonin. <br/><strong><em>Conclusion</em></strong><strong><em>:</em></strong>According to these results, it is probable that protective effects of melatonin after I/R may be mediated by vagus nerve. Therefore, there is an interaction between melatonin and vagus nerve in their protective effects.
Vagus nerve,Melatonin Ischemia/reperfusion,Oxidative stress
https://ijbms.mums.ac.ir/article_6417.html
https://ijbms.mums.ac.ir/article_6417_7b362c139baea5a2f480535f8fb62e6e.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Vitamin D3 attenuates oxidative stress and cognitive deficits in a model of toxic demyelination
80
88
EN
Sepideh
Tarbali
0000-0001-7650-1774
Department of Biology, Faculty of Science, Urmia University, Urmia, Iran
sepideh_tarbali@yahoo.com
Shiva
Khezri
0000-0001-8692-8915
Department of Biology, Faculty of Science, Urmia University, Urmia, Iran
skhezri72@gmail.com
10.22038/ijbms.2016.6418
<strong><em>Objective(s):</em></strong>Multiple sclerosis (MS) is a demyelinating disease. The prevalence of MS is highest where environmental supplies of vitamin D are low. Cognitive deficits have been observed in patients with MS. Oxidative damage may contribute to the formation of MS lesions. Considering the involvement of hippocampus in MS, an attempt is made in this study to investigate the effects of vitamin D3 on behavioral process and the oxidative status in the dorsal hippocampus (CA1 area) following the induction of experimental demyelination in rats.
<strong><em>Materials and Methods:</em></strong> Animals were divided into six groups. Control group: animals received no surgery and treatment; saline group: animals received normal saline; sham group: animals received 150 μl sesame oil IP; vitamin D3 group: animals received 5 μg/kg vitamin D3 IP; lysophosphatidyl choline (LPC) group (toxic demyelination’s model): animals received LPC by stereotaxic intra-hippocampal injection of 2 μl LPC in CA1 area; Vitamin D3- treated group: animals were treated with vitamin D3 at doses of 5 μg/kg IP for 7 and 21 days post lesion. The spatial memory, biochemical parameters including catalase (CAT) activities and lipid peroxidation levels were investigated.
<strong><em>Results:</em></strong> Animals in LPC group had more deficits in spatial memory than the control group in radial arm maze. Vitamin D3 significantly improved spatial memory compared to LPC group. Also, results indicated that vitamin D3 caused a decrease in lipid peroxidation levels and an increase in CAT activities.
<strong><em>Conclusion:</em></strong> Current findings suggest that vitamin D3 may have a protective effect on cognitive deficits and oxidative stress in toxic demyelination’s model.
Demyelination Hippocampus,Multiple Sclerosis,Oxidative stress,Vitamin D3
https://ijbms.mums.ac.ir/article_6418.html
https://ijbms.mums.ac.ir/article_6418_a029600820831b1a01547185b3547da1.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
The effect of amniotic membrane extract on umbilical cord blood mesenchymal stem cell expansion: is there any need to save the amniotic membrane besides the umbilical cord blood?
89
96
EN
Zahra
Vojdani
Laboratory for Stem Cell Research, Anatomy Department, Shiraz University of Medical Sciences, Shiraz, Iran
Ali
Babaei
Laboratory for Stem Cell Research, Anatomy Department, Shiraz University of Medical Sciences, Shiraz, Iran
babaeia@sums.ac.ir
Attiyeh
Vasaghi
Laboratory for Stem Cell Research, Anatomy Department, Shiraz University of Medical Sciences, Shiraz, Iran
Mojtaba
Habibagahi
Immunology Department, Shiraz University of Medical Sciences, Shiraz, Iran
Tahereh
Talaei-Khozani
0000-0002-8425-8871
Laboratory for Stem Cell Research, Anatomy Department, Shiraz University of Medical Sciences, Shiraz, Iran
talaeit@sums.ac.ir
10.22038/ijbms.2016.6419
<strong><em>Objective(s):</em></strong> Umbilical cord blood is a good source of the mesenchymal stem cells that can be banked, expanded and used in regenerative medicine. The objective of this study was to test whether amniotic membrane extract, as a rich source of growth factors such as basic-fibroblast growth factor, can promote the proliferation potential of the umbilical cord mesenchymal stem cells. <br/><strong><em>Materials and Methods:</em></strong> The study design was interventional. Umbilical cord mesenchymal stem cells were isolated from voluntary healthy infants from hospitals in Shiraz, Iran, cultured in the presence of basic-fibroblast growth factor and amniotic membrane extracts (from pooled - samples), and compared with control cultures. Proliferation assay was performed and duplication number and time were calculated. The expression of stem cell’s specific markers and the differentiation capacity toward osteogenic and adipogenic lineages were evaluated. <br/><strong><em>Results:</em></strong> Amniotic membrane extract led to a significant increase in the proliferation rate and duplication number and a decrease in the duplication time without any change in the cell morphology. Both amniotic membrane extract and basic-fibroblast growth factor altered the expressing of CD44 and CD105 in cell population. Treating basic-fibroblast growth factor but not the amniotic membrane extract favored the differentiation potential of the stem cells toward osteogenic lineage. <br/><strong><em>Conclusion: </em></strong>The amniotic membrane extract administration accelerated cell proliferation and modified the CD marker characteristics which may be due to the induction of differentiation toward a specific lineage. Amniotic membrane extract may enhance the proliferation rate and duplication number of the stem cell through changing the duplication time.
Amnion,Basic-fibroblast growth factor,Wharton’s jelly,Mesenchymal stem cell
https://ijbms.mums.ac.ir/article_6419.html
https://ijbms.mums.ac.ir/article_6419_32346f61c05e2fb83961ea033733d079.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Protective effect of bioactive compounds from Lonicera japonica Thunb. against H2O2-induced cytotoxicity using neonatal rat cardiomyocytes
97
105
EN
Chen
Wang
Department of Medical market, Cangzhou Central Hospital, Hebei Province, 061001, China
wangchencto@163.com
Gang
Wang
Department of Cardiology, Cangzhou Cardiovascular Research Institute, Cangzhou Central Hospital, Hebei Province, 061001, China
wanggangcto@163.com
Hong
Liu
Department of Pharmacy, General Hospital of Jixi Mining Industry Group, Heilongjiang Province, 158100, China
wanggangcto@126.com
Yun-long
Hou
Department of Pharmacy, Harbin Medical University, Heilongjiang Province, 150086, China
10.22038/ijbms.2016.6420
<strong><em>Objective(s)</em><em>:</em></strong>Pharmacological studies showed that the extracts of Jin Yin Hua and its active constituents have lipid lowering, antipyretic, hepatoprotective, cytoprotective, antimicrobial, antibiotic, antioxidative, antiviral, and anti-inflammatory effects. The purpose of the present study was to investigate the protective effects of caffeoylquinic acids (CQAs) from Jin Yin Hua against hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>)-induced and hypoxia-induced cytotoxicity using neonatal rat cardiomyocytes. <br/><strong><em>Materials and Methods</em><em>:</em></strong>Seven CQAs (C1 to C7) isolated and identified from Jin Yin Hua were used to examine the effects of H<sub>2</sub>O<sub>2</sub>-induced and hypoxia-induced cytotoxicity. We studied C4 and C6 as preventative bioactive compounds of the reactive oxygen species (ROS) production, apoptotic pathway, and apoptosis-related gene expression. <br/><strong><em>Results:</em></strong>C4 and C6 were screened as bioactive compounds to exert a cytoprotective effect against oxidative injury. Pretreatment with C4 and C6, dose-dependently attenuated hypoxia-induced ROS production and reduced the ratio of GSSG/GStotal. Western blot data revealed that the inhibitory effect of C4 on H<sub>2</sub>O<sub>2</sub>-induced up and down-regulation of Bcl-2, Bax, caspase-3, and cleaved caspase-3. Apoptosis was evaluated by detection of DNA fragmentation using TUNEL assay, and quantified with Annexin V/PI staining. <br/><strong><em>Conclusion:</em></strong><em> In vitro</em> experiments revealed that both C4 and C6 protect cardiomyocytes from necrosis and apoptosis during H2O2-induced injury, via inhibiting the generation of ROS and activation of caspase-3 apoptotic pathway. These results demonstrated that CQAs might be a class of compounds which possess potent myocardial protective activity against the ischemic heart diseases related to oxidative stress.
Anti-apoptosis,Caffeoylquinic acids,Cardiomyocytes,Lonicera japonica Thunb,Oxidative stress
https://ijbms.mums.ac.ir/article_6420.html
https://ijbms.mums.ac.ir/article_6420_1395ece368b58ab86ccfd8ea2ee23f75.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Role of peroxisome proliferator-activated receptor alpha and gamma in antiangiogenic effect of pomegranate peel extract
106
110
EN
Nasim
Dana
Applied Physiology Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran
Shaghayegh Haghjooy
Javanmard
Applied Physiology Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran
sh_haghjoo@med.mui. ac.ir
Laleh
Rafiee
Applied Physiology Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran
10.22038/ijbms.2016.6421
<strong><em>Objective(s):</em></strong> Herbal medicines are promising cancer preventive candidates. It has been shown that <em>Punica granatum </em>L. could inhibit angiogenesis and tumor invasion. In this study, we investigated whether the anti-angiogenic effect of pomegranate peel extract (PPE) is partly attributable to Peroxisome proliferator-activated receptors (PPARs) activation in the Human Umbilical Vein Endothelial Cells (HUVECs). <br/><strong><em>Materials and Methods:</em></strong> Ethanol extract from PPE was prepared. HUVECs were treated in four groups (with PPE (10 μg/ml) alone, PPE with or without PPARγ (T0070907) and α (GW6471) antagonists, and control group). The possible effect of PPARs on angiogenic regulation was checked by Matrigel assay. The mRNA expression levels of vascular endothelial growth factor (VEGF) was detected by Quantitative reverse transcription-polymerase chain reaction (QRT-PCR). <br/><strong> </strong><strong><em>Results:</em></strong> PPE significantly inhibited both tube formation (size, length, and junction of tubes) and VEGF mRNA expression (<em>P</em><0.05). Our results showed that the anti-angiogenic effects of PPE were significantly reversed by both PPAR antagonists (<em>P</em><0.05). There was no difference between PPE plus antagonists groups and the control group. <br/><strong><em>Conclusion:</em></strong> In summary our results showed that the anti-angiogenic effects of PPE could be mediated in part through PPAR dependent pathway.
Angiogenesis,Peroxisome proliferator activated receptors (PPARs),Pomegranate,Vascular Endothelial Growth Factor
https://ijbms.mums.ac.ir/article_6421.html
https://ijbms.mums.ac.ir/article_6421_8adfae732c5fef95f2fb68c11536f37a.pdf
Mashhad University of Medical Sciences
Iranian Journal of Basic Medical Sciences
2008-3866
2008-3874
19
1
2016
01
01
Ensete superbum ameliorates renal dysfunction in experimental diabetes mellitus
111
118
EN
MS
Sreekutty
Department of Biochemistry, University of Kerala, Kariavattom, Thiruvananthapuram-695581, Kerala, India
S
Mini
Department of Biochemistry, University of Kerala, Kariavattom, Thiruvananthapuram-695581, Kerala, India
minisaraswathy@gmail.com
10.22038/ijbms.2016.6422
<strong><em>Objective(s)</em><em>:</em></strong>Hyperglycemia mediated oxidative stress plays a key role in the pathogenesis of diabetic complications like nephropathy. In the present study, we evaluated the effect of ethanolic extract of <em>Ensete superbum</em> seeds (ESSE) on renal dysfunction and oxidative stress in streptozotocin-induced diabetic rats.
<strong><em>Materials and Methods</em><em>:</em></strong>Glucose, HbA1c, total protein, albumin, renal function markers (urea, uric acid and creatinine), and lipid peroxidation levels were evaluated. Renal enzymatic and non-enzymatic antioxidants were examined along with renal histopathological study.
<strong><em>Results:</em></strong>ESSE (400 mg/kg BW t) administration reduced glucose and HbA1c, and improved serum total protein and albumin in diabetic rats. ESSE in diabetic rats recorded decrement in renal function markers and renal lipid peroxidation products along with significant increment in enzymatic and non-enzymatic antioxidants. Renal morphological abnormalities of diabetic rats were markedly ameliorated by <em>E.superbum</em>.
<strong><em>Conclusion:</em></strong>These results suggest that the antioxidant effect of <em>E. superbum</em> could ameliorate oxidative stress and delay/prevent the progress of diabetic nephropathy in diabetes mellitus.
Antioxidant,Diabetes Mellitus,Diabetic nephropathy,Ensete superbum Nephroprotection,Streptozotocin
https://ijbms.mums.ac.ir/article_6422.html
https://ijbms.mums.ac.ir/article_6422_2cd1e0838c1e06fb69ecd69dcd88ebe1.pdf