دورية أكاديمية

CLC Anion/Proton Exchangers Regulate Secretory Vesicle Filling and Granule Exocytosis in Chromaffin Cells.

التفاصيل البيبلوغرافية
العنوان: CLC Anion/Proton Exchangers Regulate Secretory Vesicle Filling and Granule Exocytosis in Chromaffin Cells.
المؤلفون: Comini, Maddalena1, Sierra-Marquez, Juan1, Guzman, Gustavo2, Franzen, Arne1, Willuweit, Antje3, Katona, Istvan4, Hidalgo, Patricia1, Fahlke, Christoph1, Guzman, Raul E.1
المصدر: Journal of Neuroscience. 4/13/2022, Vol. 42 Issue 15, p3080-3095. 16p.
مستخلص: ClC-3, ClC-4, and ClC-5 are electrogenic chloride/proton exchangers that can be found in endosomal compartments of mammalian cells. Although the association with genetic diseases and the severe phenotype of knock-out animals illustrate their physiological importance, the cellular functions of these proteins have remained insufficiently understood. We here study the role of two Clcn3 splice variants, ClC-3b and ClC-3c, in granular exocytosis and catecholamine accumulation of adrenal chromaffin cells using a combination of high-resolution capacitance measurements, amperometry, protein expression/gene knock out/down, rescue experiments, and confocal microscopy. We demonstrate that ClC-3c resides in immature as well as in mature secretory granules, where it regulates catecholamine accumulation and contributes to the establishment of the readily releasable pool of secretory vesicles. The lysosomal splice variant ClC-3b contributes to vesicle priming only with low efficiency and leaves the vesicular catecholamine content unaltered. The related Cl2/H1 antiporter ClC-5 undergoes age-dependent downregulation in wild-type conditions. Its upregulation in Clcn32/2 cells partially rescues the exocytotic mutant defect. Our study demonstrates how different CLC transporters with similar transport functions, but distinct localizations can contribute to vesicle functions in the regulated secretory pathway of granule secretion in chromaffin cells. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:02706474
DOI:10.1523/JNEUROSCI.2439-21.2022