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硫化氢对体外大鼠肝星状细胞内Ca2+浓度变化及细胞增殖的影响
引用本文:尚宏伟,王利军,王兴翠,尤红,唐淑珍,高尔静,丁惠国,贾继东. 硫化氢对体外大鼠肝星状细胞内Ca2+浓度变化及细胞增殖的影响[J]. 解剖学报, 2008, 39(6): 877-880
作者姓名:尚宏伟  王利军  王兴翠  尤红  唐淑珍  高尔静  丁惠国  贾继东
作者单位:1. 首都医科大学基础医学院组织学胚胎学教研室; 2.首都医科大学附属北京佑安医院肝病消化科;3.首都医科大学附属北京友谊医院肝病中心,北京 100069
摘    要:目的 研究硫化氢(H2 S)对大鼠肝星状细胞-T6(HSC-T6) Ca2+浓度、细胞增殖的影响及其机制。 方法 活化HSC-T6用含10%小牛血清DMEM培养液制备为1×105个肝星状细胞(HSC)悬液。钙离子荧光探针Fluo-3/AM负载细胞后,在不同刺激条件下,利用激光扫描共焦显微镜动态扫描HSC-T6细胞内Ca2+荧光强度(FI)变化,FI表示细胞内Ca2+浓度。四唑盐比色法,观察不同浓度H2S供体——NaSH对HSC-T6细胞增殖的影响。 结果 低浓度H2S(100μmol/L)明显降低HSC-T6细胞内Ca2+浓度(P<0.05),而细胞增殖增加(增殖率为116%);KATP通道阻断剂——格列本脲可阻断H2S的作用。高浓度H2S(1mmol/L)刺激HSC-T6细胞内Ca2+浓度增加,但细胞增殖无明显变化(P>0.05)。 结论 低浓度H2S通过激活HSC-T6细胞KATP通道降低细胞内Ca2+浓度,可能通过调节细胞氧化应激促进细胞增殖;高浓度H2S刺激HSC-T6细胞内Ca2+浓度增加。提示H2S在肝硬化门脉高压症的发生机制中具有双重作用。

关 键 词:硫化氢  肝星状细胞  四唑盐比色法  激光扫描共焦显微镜  细胞培养  大鼠

EFFECTS OF HYDROGEN SULFIDE ON INTRACELLULAR CALCIUM AND PROLIFERATION IN HEPATIC STELLATE CELLS EM>IN VITRO/EM>
SHANG Hong-wei,WANG Li-jun,WANG Xing-cui,YOU Hong,TANG Shu-zhen,GAO Er-jing,DING Hui-guo,JIA Ji-dong. EFFECTS OF HYDROGEN SULFIDE ON INTRACELLULAR CALCIUM AND PROLIFERATION IN HEPATIC STELLATE CELLS EM>IN VITRO/EM>[J]. Acta Anatomica Sinica, 2008, 39(6): 877-880
Authors:SHANG Hong-wei  WANG Li-jun  WANG Xing-cui  YOU Hong  TANG Shu-zhen  GAO Er-jing  DING Hui-guo  JIA Ji-dong
Affiliation:1. Department of Histology and Embryology, Basic Medical Science College of Capital Medical University;2.Department of Gastroenterology and Hepatology, Beijing Youan Hospital Affiliated to Capital Medical University;3. Centre of Hepatology, Friendship Beijing Hospital Affiliated to Capital Medical University, Beijing 100069, China
Abstract:Objective To study the effect of hydrogen sulfide (HSUB>2/SUB>S) on intracellular calcium concentration and proliferation in hepatic stellate cells (HSC) and the possible mechanism of HSUB>2/SUB>S. Methods HSC-T6, an activated rat HSC, was plated in 35-mm culture dish at a density of 1×10SUP>5/SUP>/ml, and rotuinely incubated in DMEM media for 24 hours. The intracellular CaSUP>2+/SUP> loaded by Flu-3/AM was measured by laser scanning confocal microscope. The dynamic changes of intracellular CaSUP>2+/SUP> fluorescence intensity([CaSUP>2+/SUP>]i ) stimulated by NaSH, a HSUB>2/SUB>S donor, were measured. The HSC proliferations were measured by MTT at different HSUB>2/SUB>S concentrations. Results Low concentration of HSUB>2/SUB>S(100μmol/L) decreased significantly HSC-T6 [CaSUP>2+/SUP>]i (16.20±3.56 vs 14.12±3.76,EM>P/EM><0.05). The increased HSC-T6 proliferations were also observed in low concentration stimulation of HSUB>2/SUB>S(50-100μmol/L). The decreased [CaSUP>2+/SUP>]i was inhibited by glibenclamide, a KSUB>ATP/SUB> channel antagonist, significantly when administered with HSUB>2/SUB>S of higher concentrations. However, high concentration of HSUB>2/SUB>S(1mmol/L) increased significantly HSC-T6 [CaSUP>2+/SUP>]i,P<0.05, with no significant changes in proliferation. Conclusion Th
Keywords:Hydrogen sulfide  Hepatic stellate cell  MTT  Laser scanning confocal microscope  Cell culture  Rat
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