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Tuning the Size of Large Dense‐Core Vesicles and Quantal Neurotransmitter Release via Secretogranin II Liquid–Liquid Phase Separation
Large dense‐core vesicles (LDCVs) are larger in volume than synaptic vesicles, and are filled with multiple neuropeptides, hormones, and neurotransmitters that participate in various physiological processes. However, little is known about the mechanism determining the size of LDCVs. Here, it is repo...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9507364/ https://www.ncbi.nlm.nih.gov/pubmed/35896896 http://dx.doi.org/10.1002/advs.202202263 |
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author | Lin, Zhaohan Li, Yinglin Hang, Yuqi Wang, Changhe Liu, Bing Li, Jie Yin, Lili Jiang, Xiaohan Du, Xingyu Qiao, Zhongjun Zhu, Feipeng Zhang, Zhe Zhang, Quanfeng Zhou, Zhuan |
author_facet | Lin, Zhaohan Li, Yinglin Hang, Yuqi Wang, Changhe Liu, Bing Li, Jie Yin, Lili Jiang, Xiaohan Du, Xingyu Qiao, Zhongjun Zhu, Feipeng Zhang, Zhe Zhang, Quanfeng Zhou, Zhuan |
author_sort | Lin, Zhaohan |
collection | PubMed |
description | Large dense‐core vesicles (LDCVs) are larger in volume than synaptic vesicles, and are filled with multiple neuropeptides, hormones, and neurotransmitters that participate in various physiological processes. However, little is known about the mechanism determining the size of LDCVs. Here, it is reported that secretogranin II (SgII), a vesicle matrix protein, contributes to LDCV size regulation through its liquid–liquid phase separation in neuroendocrine cells. First, SgII undergoes pH‐dependent polymerization and the polymerized SgII forms phase droplets with Ca(2+) in vitro and in vivo. Further, the Ca(2+)‐induced SgII droplets recruit reconstituted bio‐lipids, mimicking the LDCVs biogenesis. In addition, SgII knockdown leads to significant decrease of the quantal neurotransmitter release by affecting LDCV size, which is differently rescued by SgII truncations with different degrees of phase separation. In conclusion, it is shown that SgII is a unique intravesicular matrix protein undergoing liquid–liquid phase separation, and present novel insights into how SgII determines LDCV size and the quantal neurotransmitter release. |
format | Online Article Text |
id | pubmed-9507364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95073642022-09-30 Tuning the Size of Large Dense‐Core Vesicles and Quantal Neurotransmitter Release via Secretogranin II Liquid–Liquid Phase Separation Lin, Zhaohan Li, Yinglin Hang, Yuqi Wang, Changhe Liu, Bing Li, Jie Yin, Lili Jiang, Xiaohan Du, Xingyu Qiao, Zhongjun Zhu, Feipeng Zhang, Zhe Zhang, Quanfeng Zhou, Zhuan Adv Sci (Weinh) Research Articles Large dense‐core vesicles (LDCVs) are larger in volume than synaptic vesicles, and are filled with multiple neuropeptides, hormones, and neurotransmitters that participate in various physiological processes. However, little is known about the mechanism determining the size of LDCVs. Here, it is reported that secretogranin II (SgII), a vesicle matrix protein, contributes to LDCV size regulation through its liquid–liquid phase separation in neuroendocrine cells. First, SgII undergoes pH‐dependent polymerization and the polymerized SgII forms phase droplets with Ca(2+) in vitro and in vivo. Further, the Ca(2+)‐induced SgII droplets recruit reconstituted bio‐lipids, mimicking the LDCVs biogenesis. In addition, SgII knockdown leads to significant decrease of the quantal neurotransmitter release by affecting LDCV size, which is differently rescued by SgII truncations with different degrees of phase separation. In conclusion, it is shown that SgII is a unique intravesicular matrix protein undergoing liquid–liquid phase separation, and present novel insights into how SgII determines LDCV size and the quantal neurotransmitter release. John Wiley and Sons Inc. 2022-07-27 /pmc/articles/PMC9507364/ /pubmed/35896896 http://dx.doi.org/10.1002/advs.202202263 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Lin, Zhaohan Li, Yinglin Hang, Yuqi Wang, Changhe Liu, Bing Li, Jie Yin, Lili Jiang, Xiaohan Du, Xingyu Qiao, Zhongjun Zhu, Feipeng Zhang, Zhe Zhang, Quanfeng Zhou, Zhuan Tuning the Size of Large Dense‐Core Vesicles and Quantal Neurotransmitter Release via Secretogranin II Liquid–Liquid Phase Separation |
title | Tuning the Size of Large Dense‐Core Vesicles and Quantal Neurotransmitter Release via Secretogranin II Liquid–Liquid Phase Separation |
title_full | Tuning the Size of Large Dense‐Core Vesicles and Quantal Neurotransmitter Release via Secretogranin II Liquid–Liquid Phase Separation |
title_fullStr | Tuning the Size of Large Dense‐Core Vesicles and Quantal Neurotransmitter Release via Secretogranin II Liquid–Liquid Phase Separation |
title_full_unstemmed | Tuning the Size of Large Dense‐Core Vesicles and Quantal Neurotransmitter Release via Secretogranin II Liquid–Liquid Phase Separation |
title_short | Tuning the Size of Large Dense‐Core Vesicles and Quantal Neurotransmitter Release via Secretogranin II Liquid–Liquid Phase Separation |
title_sort | tuning the size of large dense‐core vesicles and quantal neurotransmitter release via secretogranin ii liquid–liquid phase separation |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9507364/ https://www.ncbi.nlm.nih.gov/pubmed/35896896 http://dx.doi.org/10.1002/advs.202202263 |
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