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骨髓间充质干细胞移植对大鼠肝纤维化模型的修复作用 被引量:4

Repairment of marrow derived mesenchymal stem cells on hepatic fibrosis in rats
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摘要 目的:观察骨髓间充质干细胞(MSCs)移植对大鼠肝纤维化模型的修复作用,为MSCs的临床应用提供可靠的理论依据。方法:分离、纯化大鼠MSCs并进行体外培养。用皮下多点注射CCl4制备肝纤维化大鼠模型,将大鼠随机分为3组:正常对照组、模型损伤组和MSCs移植组,每组6只。将MSCs经尾静脉回输到MSCs移植组大鼠体内,30 d取肝脏,观察病理变化,免疫组织化学检测α平滑肌肌动蛋白(α-SMA)的表达。结果:流式细胞术检测体外分离培养的MSCs 93.27%处于G0/G1期,且MSCs表面CD44呈阳性表达;将分离的MSCs输入肝纤维化模型大鼠30 d后,镜下可见MSCs移植组病理改变较模型损伤组明显减轻,肝小叶结构基本正常,肝血窦基本正常,纤维结缔组织无明显增生;α-SMA染色强度MSCs移植组低于模型损伤组。结论:MSCs在一定程度上可以促进纤维化肝组织的修复。 Objective To observe the repairing effect of marrow derived mesenchymal stem cells(MSCs) on hepatic fibrosis in rats,and provide a reliable theoretical basis for further clinical application of MSCs.Methods The MSCs of rats were isolated,purified and cultivated in vitro.The model of hepatic fibrosis induced by CCl4 was established.The rats were divided into three groups:normal control group,model group,MSCs transplantation group,6 each group.The MSCs were transplatated into the rats through tail vein in MSCs transplantation group.The repairing effect of MSCs on hepatic fibrosis was observed and the expression of α-SMA in liver tissue was detected by immunohistochemistry 30 d after transplantation.Results 93.27% MSCs were at G0/G1 phase,and the CD44 surface expression in the MSCs was positive.The hepatic pathological injury changes of rats in MSCs transplantation group were significantly reduced than that in model group 30 d after MSCs injection.The lobular structure and liver sinusoids were normal and hyperplasia of fibrous connective tissue was not obvious.The intensity of α-SMA staining in MSCs transplantation group was lower than that in model group.Conclusion MSCs have repairment on hepatic fibrosis in rats to a certain extent.
出处 《吉林大学学报(医学版)》 CAS CSCD 北大核心 2009年第5期874-876,I0002,共4页 Journal of Jilin University:Medicine Edition
基金 吉林省科技厅科研基金资助课题(20080446)
关键词 骨髓间充质干细胞 肝纤维化 Α-SMA 组织修复 mesenehymal stem cells hepatic fibrosis α-SMA tissue repair
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参考文献12

  • 1Pol S, Carnot F, Nalpas B, et al. Reversibility of hepatitis C virus-related cirrhosis [J]. Hum Pathol, 2004, 35 (1): 107-112.
  • 2Muretto P, Angelucci E, Lucarelli G. Reversibility of cirrhosis in patients cured of thalassemia by bone marrow transplantation [J]. Ann Intern Med, 2002, 136 (9): 667- 672.
  • 3Ong SY, Dai H, Leong KW. Inducing hepatic differentiation of hurnan mesenchymal stem cells in pellet culture [J].Biomaterials, 2006, 27 (22): 4087-4097.
  • 4郝瑞锋,申长虹.骨髓间充质干细胞向成骨细胞诱导的研究现状[J].天津医科大学学报,2007,13(1):129-131. 被引量:17
  • 5刘厂辉,阳辉,游三丽,郭慧.永生型兔骨髓间充质干细胞定向诱导分化为脂肪细胞的实验研究(英文)[J].中国现代医学杂志,2008,18(3):257-261. 被引量:2
  • 6Wislet-Gendebien S, Hans G, Lep rince P, et al. Plastieityof culturedmesenchymal stem cells: switch from nestin-pos-itive to excitable neuron-like phenotype [J]. Stem Cells, 2005, 23 (3): 392-402.
  • 7Heng BC, Haider HKh, Sire EK, et al. Strategies for directing the differentiation of stem cells into the cardiomyogenic lineage in vitro[J].Cardiovasc Res, 2004, 62 (1): 34-42.
  • 8Wang X, Montini E, AI-Dhalimy M, et al. Kinetics ofliver repopulation after bone marrow transp lantation [J]. Am J Pathol, 2002, 161 (2): 565-574.
  • 9Ong SY, Dai H, Leong KW. Hepatic differentiation potential of commercially available human mesenchymal stem cells[J]. Tissue Eng, 2006, 8 (5): 480-487.
  • 10Inderbitzin D, Avital I, Gloor B, et al. Funetional comparison of bone marrow derived liver stem cells: selseetion strategy for cell-based therapy[J]. Gastrointest Surg, 2005, 9 (9): 1340-1345.

二级参考文献36

  • 1康新勤,臧伟进,胥晓丽,宋土生,于晓江,曾菊绒.大鼠骨髓间充质干细胞定向成骨细胞分化中碱性磷酸酶的变化[J].西安交通大学学报(医学版),2004,25(4):366-368. 被引量:7
  • 2程志安,周敦华,宋少云,吴燕峰,沈慧勇,曾志勇,刘尚礼.脐血与骨髓间充质干细胞的成骨细胞定向诱导及其成骨活性比较[J].中国临床康复,2004,8(35):7973-7975. 被引量:15
  • 3Erices A, Conget P, Minguell JJ. Mesenchymal progenitor cells in human umbilical cord blood [J]. Br J Haematol, 2000,109 ( 1 ) :235.
  • 4Zohar R, Sodek J, Mcculloch CA. Characterization of stromal progenitor cells enriched by flowcytometry [J]. Blood, 1997, 90(9):3 471.
  • 5Fortier LA, Nixon AJ, Williams J, et al. Isolation and chondrocytic differentiation of equine bone marrow-derived mesenchymal stem cells [J]. Am J Vet Res, 1998,59(9):1182.
  • 6Ghilzo R, Mcctdloch CA, Zohar R. Stromal mesenchymal progenitor cells [J]. Leukemia Lymphoma, 1999,32(3/4):211.
  • 7Nuttal ME, Patton A J, Olivera DL, et al. Human trabccular bone cells are able to express both osteoblastic and adipocytic phenotype:implications for osteopenic disorders [J]. L Bone Miner Res, 1998,13(3):371.
  • 8Mandana Mohyeddin Bonab, Kamran alimoghaddam, Fatemeh Talebian,et al. Aging of mesenchymal stem cell in vitro [J]. BMC Cell Biol,2006, 7:14.
  • 9Kim HJ, Zhao Hb, Kitaura H, et al. Glucocorticoids suppress bone formation via the osteoclast [J]. J Clin Invest, 2006, 16(8):2152.
  • 10Jaiswal N, Haynesworth SE, Caplan AI, et al. Osteogenic differentiation of purifield, Culture-expanded human mesenchymal stem cells in vito [J]. Cell Biochem, 1997, 64(2):295.

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