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胰岛细胞中多囊泡体和分泌颗粒的定位与释放比较:2型糖尿病期间的失调

Comparison of localization and release of multivesicular bodies and secretory granules in islet cells: Dysregulation during type-2 diabetes.

作者信息

Veerabhadraswamy Priyadarshini, Lata Kiran, Dey Sristi, Belekar Prajakta, Kothegala Lakshmi, Mangala Prasad Vidya, Gandasi Nikhil R

机构信息

Cell Metabolism Lab (GA-08), Department of Developmental Biology and Genetics (DBG) Indian Institute of Science (IISc) Bengaluru India.

Molecular Biophysics Unit Indian Institute of Science Bengaluru Karnataka India.

出版信息

J Extracell Biol. 2024 Nov 29;3(11):e70014. doi: 10.1002/jex2.70014. eCollection 2024 Nov.

Abstract

Multivesicular bodies (MVBs) are vesicles of endosomal origin containing intraluminal vesicles, which upon fusion with plasma membrane, secrete exosomes. They play a significant role in the physiology and pathology of type-2 diabetes (T2D) due to disrupted intercellular communication. The role of MVBs and their influence on insulin secretory granules (ISGs) of β-cells or their characterization is yet to be uncovered. In our study, we compared MVBs to largely well-characterized ISGs in β-cells. This study compares the density, localization, and exocytosis of CD63+ compartments (CD63+c) with NPY labelled ISGs (NISGs) in β-cells. For this, tetraspanin CD63 was exploited to majorly label MVBs in β-cells. These labels preserve the structural integrity of labelled compartments and mostly do not localize with other endo-lysosomal compartments. This study showed that the β-cells have a significantly higher density of NISGs than CD63+c. CD63+c and NISGs are spatially localized apart within β-cells. The proteins that localize with CD63+c are different from the ones that localize with NISGs. Exocytosis of NISGs occurs at the periphery of the β-cells and takes significantly less time when compared to the release of CD63+c, which is non-peripheral and takes a longer duration. Mechanistically, the availability of CD63+c for exocytosis was assessed and found that an equilibrium is maintained between docking and undocking states at the plasma membrane. Although there are a high number of short-term residing, visiting CD63+c at the plasma membrane, the availability of CD63+c for exocytosis is maintained due to docking and undocking states. Further, a significant reduction in the density of NISGs and CD63+c was observed in β-cells isolated from T2D donors compared to healthy counterparts. Studying the effect of MVBs on insulin secretion in physiological and T2D conditions has huge potential. This study provides a strong basis to open new avenues for such future studies.

摘要

多囊泡体(MVBs)是源自内体的囊泡,含有腔内囊泡,与质膜融合后会分泌外泌体。由于细胞间通讯中断,它们在2型糖尿病(T2D)的生理和病理过程中发挥着重要作用。MVBs的作用及其对β细胞胰岛素分泌颗粒(ISGs)的影响或其特征尚未明确。在我们的研究中,我们将MVBs与β细胞中特征较为明确的ISGs进行了比较。本研究比较了β细胞中CD63 +区室(CD63 + c)与神经肽Y标记的ISGs(NISGs)的密度、定位和胞吐作用。为此,利用四跨膜蛋白CD63主要标记β细胞中的MVBs。这些标记物保留了标记区室的结构完整性,并且大多不与其他内溶酶体区室定位在一起。本研究表明,β细胞中NISGs的密度显著高于CD63 + c。CD63 + c和NISGs在β细胞内空间定位不同。与CD63 + c定位在一起的蛋白质与与NISGs定位在一起的蛋白质不同。NISGs的胞吐作用发生在β细胞的周边,与非周边且持续时间较长的CD63 + c释放相比,所需时间明显更短。从机制上讲,评估了CD63 + c用于胞吐作用的可用性,发现在质膜上对接和未对接状态之间保持着平衡。尽管在质膜上有大量短期存在、短暂停留的CD63 + c,但由于对接和未对接状态,CD63 + c用于胞吐作用的可用性得以维持。此外,与健康供体分离的β细胞相比,从T2D供体分离的β细胞中观察到NISGs和CD63 + c的密度显著降低。研究MVBs在生理和T2D条件下对胰岛素分泌的影响具有巨大潜力。本研究为开展此类未来研究开辟新途径提供了有力依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e089/11605659/fe8c7ba0f3a7/JEX2-3-e70014-g007.jpg

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