Sodium nitroprusside promoting the migration of vein transplanted bone marrow mesenchymal stem cells to the colon of ulcerative colitis rat

CHEN Xiao-yun; et al

doi:10.13406/j.cnki.cyxb.2011.02.016

您当前的位置：

首页 >

文章列表页 >

Sodium nitroprusside promoting the migration of vein transplanted bone marrow mesenchymal stem cells to the colon of ulcerative colitis rat

更新时间：2024-01-17

- Sodium nitroprusside promoting the migration of vein transplanted bone marrow mesenchymal stem cells to the colon of ulcerative colitis rat
- Journal of Chongqing Medical University Vol. 36, Issue 2, Pages: 152-155(2011)
- 作者机构：
  
  重庆医科大学基础医学院组织学与胚胎学教研室干细胞与组织工程研究室
- 作者简介：
- 基金信息：
- DOI：10.13406/j.cnki.cyxb.2011.02.016
  CLC： R574.62
- Published：2011，
扫描看全文
[1]陈晓云,徐艳华,姜蓉,汪维伟.硝普钠促进静脉移植BMSCs向溃疡性结肠炎大鼠结肠的迁移[J].重庆医科大学学报,2011,36(02):152-155.

CHEN Xiao-yun, et al. Sodium nitroprusside promoting the migration of vein transplanted bone marrow mesenchymal stem cells to the colon of ulcerative colitis rat. [J]. Journal of Chongqing Medical University 36(2):152-155(2011)
[1]陈晓云,徐艳华,姜蓉,汪维伟.硝普钠促进静脉移植BMSCs向溃疡性结肠炎大鼠结肠的迁移[J].重庆医科大学学报,2011,36(02):152-155. DOI： 10.13406/j.cnki.cyxb.2011.02.016.

CHEN Xiao-yun, et al. Sodium nitroprusside promoting the migration of vein transplanted bone marrow mesenchymal stem cells to the colon of ulcerative colitis rat. [J]. Journal of Chongqing Medical University 36(2):152-155(2011) DOI： 10.13406/j.cnki.cyxb.2011.02.016.

摘要

目的:观察硝普钠能否促进静脉移植的大鼠骨髓间充质干细胞（Bone marrow mesenchymal stem cells

BMSCs）向溃疡性结肠炎（Ulcerativecolitis

UC）大鼠结肠的迁移。方法:分离培养4、’

6-二脒基-2-苯基吲哚盐酸（4’

6-diamidino-2-phenylindole

DAPI）荧光标记SD大鼠BMSCs。免疫复合法建立UC大鼠模型

1、2组UC大鼠均经尾静脉注射DAPI标记BMSCs的细胞悬液

2组细胞悬液还含0.2 mg/kg体重的硝普钠。移植后第7、14天各处死5只大鼠

取溃疡及非溃疡部位结肠做恒冷切片

荧光显微镜下分别计数各组DAPI标记BMSCs在溃疡及非溃疡部位结肠的细胞数。结果:移植第7、14天

2组结肠溃疡部位阳性细胞数均明显高于非溃疡部位（P<0.01）;移植第7天

2组溃疡及非溃疡部位的阳性细胞数均高于1组（P<0.05）。结论:静脉移植BMSCs的同时给予硝普钠能促进BMSCs向结肠溃疡部位的迁移。

Abstract

Objective:To investigate the effect of Sodium nitroprusside(SNP) in promoting the migration of vein transplanted bone marrow mesenchymal stem cells(BMSCs)to the colon of ulcerative colitis rat.Methods:BMSCs of SD rat were isolated

cultured and marked with DAPI.Ulcerative colitis(UC) rat was induced with immune-combined TNBS/ethanol.UC rats in group 1 and 2 was received caudal vein injection of DAPI labeled BMSCs cell suspension;but 0.2 mg Sodium nitroprusside/kg body weight was also injected in group 2.5 rats in each group were sacrificed on day 7 and 14 after injection.The colon of ulcerative or non-ulcerative parts were prepared as cryostat sections.The numbers of BMSCs both in colon of ulcerative or non-ulcerative parts were counted under fluorescent microscope respectively.Results:On the 7th and 14th day after injection

the number of marked BMSCs in the colonic ulcerative part was more than that in non-ulcerative parts(P< 0.01) both in group 1 and 2;On the 7th day

the marked BMSCs number of group 2 both in the colon of ulcerative or non-ulcerative parts were higher than those in group 1(P<0.05).Conclusion:SNP could encourage vein transplanted BMSCs migranting to the injured colonic tissue by the way that vein transplantion of BMSCs combined supply of SNP at the same time.

关键词

骨髓间充质干细胞移植溃疡性结肠炎硝普钠

Keywords

bone marrow mesenchymal stem cellstransplantationulcerative colitissodium nitroprusside

references

Views

下载量

CSCD

Alert me when the article has been cited

提交

Tools

Publicity Resources

Distribution of transplanted bone mesenchymal stem cells in colon of ulcerative colitis rat

Endosomatic transference of transplanted bone marrow mesenchymal stem cells in rat of ulcerative colitis

Effects of autologous bone marrow mesenchymal stem cells on the renal cell proliferation and apoptosis and renal function in a rabbit of renal ischemia-reperfusion injury

Intervention effect of coix seed polysaccharides on an in vitro inflammation model of ulcerative colitis and its mechanism: a study based on the NLRP3/caspase-1 pathway

Influence of tripterygium wilfordii polyglycoside on coagulation function of rats with ulcerative colitis

Related Author

CHEN Xiao-Yun

et al

姜蓉

汪维伟

DUAN Zheng

et al

陈小云

汪维伟

Related Institution

Department of Histology and Embryology ,Laboratory of Stem Cells and Tissue Engineering,Chongqing Medical University

Department of Histology and Embryology,College of Basic Medicina,Chongqing Medical University

Renal Diseases Research Center,Departmentv of Urinary Surgery,Xinqiao Hospital,the Third Military Medical University

贵州省习水县人民医院外一科

School of Integrated Traditional Chinese and Western Medicine，Gansu University of Chinese Medicine

⁰