CAPS facilitates filling of the rapidly releasable pool of large dense-core vesicles.

نویسندگان

  • Yuanyuan Liu
  • Claudia Schirra
  • David R Stevens
  • Ulf Matti
  • Dina Speidel
  • Detlef Hof
  • Dieter Bruns
  • Nils Brose
  • Jens Rettig
چکیده

Calcium-activator protein for secretion (CAPS) is a cytosolic protein that associates with large dense-core vesicles and is involved in their secretion. Mammals express two CAPS isoforms, which share a similar domain structure including a Munc13 homology domain that is believed to be involved in the priming of secretory vesicles. A variety of studies designed to perturb CAPS function indicate that CAPS is involved in the secretion of large dense-core vesicles, but where in the secretory pathway CAPS acts is still under debate. Mice in which one allele of the CAPS-1 gene is deleted exhibit a deficit in catecholamine secretion from chromaffin cells. We have examined catecholamine secretion from chromaffin cells in which both CAPS genes were deleted and show that the deletion of both CAPS isoforms causes a strong reduction in the pool of rapidly releasable chromaffin granules and of sustained release during ongoing stimulation. We conclude that CAPS is required for the adequate refilling and/or maintenance of a rapidly releasable granule pool.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Two distinct secretory vesicle–priming steps in adrenal chromaffin cells

Priming of large dense-core vesicles (LDCVs) is a Ca(2+)-dependent step by which LDCVs enter a release-ready pool, involving the formation of the soluble N-ethyl-maleimide sensitive fusion protein attachment protein (SNAP) receptor complex consisting of syntaxin, SNAP-25, and synaptobrevin. Using mice lacking both isoforms of the calcium-dependent activator protein for secretion (CAPS), we show...

متن کامل

Molecular characterization of two distinct secretory vesicle priming steps in adrenal chromaffin cells

Priming of large dense-core vesicles (LDCVs) is a Ca-dependent step by which LDCVs enter a release-ready pool. The underlying molecular step involves the formation of the SNAREcomplex consisting of syntaxin, SNAP-25 and synaptobrevin, which is facilitated by priming proteins such as Munc13s. By using mutant mice lacking both isoforms of the calcium dependent activator protein for secretion (CAP...

متن کامل

Monitoring of insulin granule packaging in live cells using homoFRET-FP detection

Fig. 1: Insulin production and storage. Key biological steps in insulin production: 1) Transcription, 2) translation and translocation to the endoplasmic reticulum, 3) folding and signal peptide cleavage 4) Golgi transport and packaging into secretory vesicles 5) cleavage to produce mature insulin. Mature insulin is stored in dense-core granules in two populations: RRP = ready releasable pool a...

متن کامل

Intracellular calcium dependence of large dense-core vesicle exocytosis in the absence of synaptotagmin I.

Synaptotagmin I is a synaptic vesicle-associated protein essential for synchronous neurotransmission. We investigated its impact on the intracellular Ca(2+)-dependence of large dense-core vesicle (LDCV) exocytosis by combining Ca(2+)-uncaging and membrane capacitance measurements in adrenal slices from mouse synaptotagmin I null mutants. Synaptotagmin I-deficient chromaffin cells displayed prol...

متن کامل

Endocytosis and vesicle recycling at a ribbon synapse.

At ribbon synapses, where exocytosis is regulated by graded depolarization, vesicles can fuse very rapidly with the plasma membrane (complete discharge of the releasable pool in approximately 200 msec). Vesicles are also retrieved very rapidly (time constant of approximately 1 sec), leading us to wonder whether their retrieval uses an unusual mechanism. To study this, we exposed isolated bipola...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • The Journal of neuroscience : the official journal of the Society for Neuroscience

دوره 28 21  شماره 

صفحات  -

تاریخ انتشار 2008