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膜片钳记录单个胰腺酶原颗粒:直接测量颗粒膜上的离子通道活性。

Patch clamped single pancreatic zymogen granules: direct measurements of ion channel activities at the granule membrane.

作者信息

Kelly Marie L, Abu-Hamdah Rania, Jeremic Aleksandar, Cho Sang-Joon, Ilie Alina-Elena, Jena Bhanu P

机构信息

Department of Physiology, Wayne State University School of Medicine, Detroit, MI 48201, USA.

出版信息

Pancreatology. 2005;5(4-5):443-9. doi: 10.1159/000086556. Epub 2005 Jun 28.

Abstract

BACKGROUND/AIM: Pancreatic acinar cells are involved in the secretion of digestive enzymes. Digestive enzymes in pancreatic acinar cells are stored in membrane-bound secretory vesicles called zymogen granules (ZGs). The swelling of ZGs is implicated in the regulation of the expulsion of intravesicular contents during secretion. The molecular mechanism of ZG swelling has been previously elucidated. It has been further demonstrated that the water channel aquaporin-1, the potassium channel IRK-8, and the chloride channel CLC-2, are present in the ZG membrane and involved in ZG swelling. However, a direct measurement of these ion channels at the ZG membrane in intact ZGs had not been performed. The aim of this study was to investigate the electrical activity of single ZGs and verify the types of channels found within their membrane.

METHODS

ZGs from pancreatic acinar cells were isolated from the pancreas of Sprague-Dawley rats. Direct measurements of whole vesicle currents, in the presence and absence of ion channel blockers (quinine, glyburide and DIDS), were recorded following successful patching of single ZGs.

CONCLUSION

In this study, we were able, for the first time, to patch single ZGs and study ion channels in their membrane. We were able to record currents across the ZG membrane and, utilizing ion channel blockers, confirm the presence of the chloride channels CLC-2 and the potassium channel IRK-8 (Kir6.1), and additionally demonstrate the presence of a second chloride channel CLC-3.

摘要

背景/目的:胰腺腺泡细胞参与消化酶的分泌。胰腺腺泡细胞中的消化酶储存在称为酶原颗粒(ZGs)的膜结合分泌小泡中。酶原颗粒的肿胀与分泌过程中泡内内容物的排出调节有关。酶原颗粒肿胀的分子机制此前已得到阐明。进一步的研究表明,水通道水通道蛋白-1、钾通道IRK-8和氯通道CLC-2存在于酶原颗粒膜中,并参与酶原颗粒的肿胀。然而,尚未对完整酶原颗粒的酶原颗粒膜上的这些离子通道进行直接测量。本研究的目的是研究单个酶原颗粒的电活动,并验证其膜内发现的通道类型。

方法

从Sprague-Dawley大鼠的胰腺中分离出胰腺腺泡细胞的酶原颗粒。在成功封接单个酶原颗粒后,记录有无离子通道阻滞剂(奎宁、格列本脲和二异丙基氟磷酸)时的全泡电流。

结论

在本研究中,我们首次能够封接单个酶原颗粒并研究其膜上的离子通道。我们能够记录跨酶原颗粒膜的电流,并利用离子通道阻滞剂证实氯通道CLC-2和钾通道IRK-8(Kir6.1)的存在,此外还证明了第二种氯通道CLC-3的存在。

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