Dynamic recruitment of Munc13 primes docked secretory granules for exocytosis

Munc13 proteins are essential for regulated exocytosis in neurons and endocrine cells. They consist of an elongated MUN domain that templates SNARE complex formation during priming, flanked by regulatory membrane-associated C1 and C2 domains. Here, we show, using quantitative high-resolution imaging, that priming of insulin granules coincides with recruitment of on average six copies of Munc13 to individual docked granules, similar to estimates of SNARE complexes formed during exocytosis. Intracellular Ca<sup>2+</sup>- or lipid-signaling accelerates granule priming by promoting C2B-dependent translocation of Munc13 to the plasma membrane, followed by slower (tens of seconds) C2A-domain dependent accumulation at docked granules. Exocytosis in human β-cells also exhibits rapid Ca<sup>2+</sup>-dependent short-term facilitation that involves Ca<sup>2+</sup>/C2B-dependent activation of Munc13 but not further accumulation at the release site. Thus, Munc13 controls secretory granule release probability by two separate C2B-dependent mechanisms that affect its recruitment to the release site and its subsequent activation by Ca<sup>2+</sup>.

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Publication Details

Journal
Cell Reports
Published
2025-09-17
DOI
https://doi.org/10.1016/j.celrep.2025.116301
Citations
1
Primary Topic
Cellular transport and secretion
Type
article
Field-Weighted Citation Impact
1.15
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Dynamic recruitment of Munc13 primes docked secretory granules for exocytosis

Sebastian Barg, Santiago Echeverry, Johan Dunevall, Nikhil R. Gandasi et al.
1 citations
Cell Reports
Cellular transport and secretion
1.15
article

Dynamic recruitment of Munc13 primes docked secretory granules for exocytosis

Sebastian Barg, Santiago Echeverry, Johan Dunevall, Nikhil R. Gandasi, Per-Eric Lund, Jan Saras
article en
1 citations

Abstract

Munc13 proteins are essential for regulated exocytosis in neurons and endocrine cells. They consist of an elongated MUN domain that templates SNARE complex formation during priming, flanked by regulatory membrane-associated C1 and C2 domains. Here, we show, using quantitative high-resolution imaging, that priming of insulin granules coincides with recruitment of on average six copies of Munc13 to individual docked granules, similar to estimates of SNARE complexes formed during exocytosis. Intracellular Ca<sup>2+</sup>- or lipid-signaling accelerates granule priming by promoting C2B-dependent translocation of Munc13 to the plasma membrane, followed by slower (tens of seconds) C2A-domain dependent accumulation at docked granules. Exocytosis in human β-cells also exhibits rapid Ca<sup>2+</sup>-dependent short-term facilitation that involves Ca<sup>2+</sup>/C2B-dependent activation of Munc13 but not further accumulation at the release site. Thus, Munc13 controls secretory granule release probability by two separate C2B-dependent mechanisms that affect its recruitment to the release site and its subsequent activation by Ca<sup>2+</sup>.

Cell ReportsVol. 44(10)
Uppsala University (SE)
Openalex Percentile: Top 20%
Cellular transport and secretion
1.15
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