State Key Laboratory of Membrane Biology and Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, College of Future Technology, Peking-Tsinghua Center for Life Sciences, and PKU-IDG/McGovern Institute for Brain Research, Peking University, Beijing, 100871, China.
Adv Sci (Weinh). 2022 Sep;9(27):e2202263. doi: 10.1002/advs.202202263. Epub 2022 Jul 27.
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 in vitro and in vivo. Further, the Ca -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.
大致密核心囊泡 (LDCVs) 比突触小泡体积更大,其内充满了多种参与各种生理过程的神经肽、激素和神经递质。然而,关于决定 LDCV 大小的机制知之甚少。本文报道,囊泡基质蛋白分泌颗粒蛋白 II (SgII) 通过其在神经内分泌细胞中的液-液相分离,有助于 LDCV 大小的调节。首先,SgII 经历 pH 依赖性聚合,聚合的 SgII 在体外和体内与 Ca 形成相分离液滴。此外,Ca 诱导的 SgII 液滴募集重建的生物脂类,模拟 LDCV 的生物发生。此外,SgII 敲低会通过影响 LDCV 大小导致量子神经递质释放显著减少,而不同程度相分离的 SgII 截断可不同程度地挽救这一现象。总之,研究表明 SgII 是一种独特的囊内基质蛋白,经历液-液相分离,并为 SgII 如何决定 LDCV 大小和量子神经递质释放提供了新的见解。