首页|牛磺胆酸钠依赖于胞外钙离子而非活性氧途径激活小鼠胰腺腺泡细胞氯通道

牛磺胆酸钠依赖于胞外钙离子而非活性氧途径激活小鼠胰腺腺泡细胞氯通道

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目的:探讨牛磺胆酸钠对小鼠胰腺腺泡细胞氯通道的激活作用及途径.方法:胶原蛋白酶消化分离FVB/N小鼠胰腺腺泡细胞,采用膜片钳技术记录牛磺胆酸钠激活的全细胞电流;去除电极内液配方中的三磷酸腺苷(ATP),观察其胞内ATP依赖性;阴离子置换实验分析其阴离子选择性;利用氯通道阻断剂检测其药理学特性;采用47%高渗灌流液观察其容积敏感性;清除胞外等渗灌流液中的Ca2+分析通道激活对胞外Ca2+的依赖性;使用透膜荧光探针2',7'-二氯荧光黄双乙酸盐检测胞内活性氧(ROS)水平.结果:5 mmol/L牛磺胆酸钠可激活小鼠胰腺腺泡细胞产生电流,该电流呈外向整流优势,对细胞内液的ATP具有依赖性,其阴离子通透性顺序为:I->Br-≥Cl->gluconate-(P<0.01);该电流能被氯通道阻断剂4,4'-二异硫氰酸十八烯-2,2'-二磺酸二钠盐水合物(DIDS)和tamoxifen抑制,且可被细胞外47%高渗刺激阻抑(P<0.01).N-乙酰-L-半胱氨酸清除细胞内ROS不能阻断牛磺胆酸钠诱导胰腺腺泡细胞产生氯电流;氯通道阻断剂DIDS不影响牛磺胆酸钠诱导的ROS生成.清除细胞外Ca2+后,牛磺胆酸钠未能诱导胰腺腺泡细胞产生氯电流.结论:牛磺胆酸钠可激活小鼠胰腺腺泡细胞氯通道,该通道的激活对胞外Ca2+具有依赖性,但不依赖于ROS途径.
A chloride channel in mouse pancreatic acinar cells is activated by so-dium taurocholate and dependent on extracellular calcium but not reac-tive oxygen species pathway
AIM:To investigate the activation of Cl-channels by sodium taurocholate(NaTC)in mouse pan-creatic acinar cells.METHODS:The single isolated pancreatic acinar cells from FVB/N mice were prepared using colla-genase digestion method.Whole-cell patch clamp technique was performed to record the currents.Intracellular adenosine triphosphate(ATP)dependence of the channels was examined via eliminating ATP from the pipette solution.Anion per-meability of the channels was investigated with ion-exchange method.The pharmacological characteristics of the channels was confirmed by two Cl-channel blockers.The volume sensitivity of the channels was detected using 47%hypertonic bathing solution.Extracellular Ca2+dependence of activating the channels was examined through eliminating Ca2+from the bathing solution.Intracellular reactive oxygen species(ROS)level was detected by an oxidation-sensitive fluorescent probe,2',7'-dichlorofluorescin diacetate.The experiment was repeated 6 times in each group.RESULTS:Extracellular application of 5 mmol/L sodium taurocholate induced a Cl-current,exhibiting the properties of outward-rectification,a se-lectivity sequence of I->Br-≥Cl->gluconate-and intracellularATP dependence(P<0.01).The currents were inhibited by chloride channel blocker 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid disodium salt hydrate(DIDS)and tamoxifen and by 47%hypertonicity stimulation(P<0.01).When ROS production was scavenged by N-acetyl-L-cysteine,the sodi-um taurocholate-induced Cl-currents were unaffected.The effect of sodium taurocholate on ROS production did not alter with the treatment with DIDS.Sodium taurocholate failed to induce Cl-currents when Ca2+was absent in extracellular bath-ing solution(P>0.05).CONCLUSION:Sodium taurocholate activates Cl-channels in mouse pancreatic acinar cells,which is dependent on extracellular Ca2+but not ROS pathway.

sodium taurocholatepancreatic acinar cellschloride channelcalciumrreactive oxygen species

阳小雅、林嘉伟、叶东、赵婵、王立伟、陈丽新

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广州卫生职业技术学院生理学教研室,广东 广州 510450

佛山市第一人民医院乳腺外一科,广东 佛山 528000

广东药科大学基础医学院,广东 广州 510006

张家界市民族中学生物教研室,湖南 张家界 427000

暨南大学基础医学与公共卫生学院,广东 广州 510632

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牛磺胆酸钠 胰腺腺泡细胞 氯离子通道 钙离子 活性氧

2022年广州市教育局高校科研项目广东省科技计划项目-对外科技合作项目2022年度广州市高等教育教学质量与教学改革工程项目

2022354232017A0505010212022JXMS029

2024

中国病理生理杂志
中国病理生理学会

中国病理生理杂志

CSTPCD北大核心
影响因子:1.065
ISSN:1000-4718
年,卷(期):2024.40(10)