Department of Molecular Biology and Genetics, Koç University, Istanbul, 34450, Turkey.
Department of Neurobiology, Max-Planck-Institute for Biophysical Chemistry, Am Faßberg 11, 37077, Göttingen, Germany.
Sci Rep. 2020 May 5;10(1):7540. doi: 10.1038/s41598-020-64486-3.
Large dense-core vesicles (LDCVs) contain a variety of neurotransmitters, proteins, and hormones such as biogenic amines and peptides, together with microRNAs (miRNAs). Isolation of LDCVs is essential for functional studies including vesicle fusion, vesicle acidification, monoamine transport, and the miRNAs stored in LDCVs. Although several methods were reported for purifying LDCVs, the final fractions are significantly contaminated by other organelles, compromising biochemical characterization. Here we isolated LDCVs (chromaffin granules) with high yield and purity from bovine adrenal medulla. The fractionation protocol combines differential and continuous sucrose gradient centrifugation, allowing for reducing major contaminants such as mitochondria. Purified LDCVs show robust acidification by the endogenous V-ATPase and undergo SNARE-mediated fusion with artificial membranes. Interestingly, LDCVs contain specific miRNAs such as miR-375 and miR-375 is stabilized by protein complex against RNase A. This protocol can be useful in research on the biological functions of LDCVs.
大致密核心囊泡 (LDCVs) 包含多种神经递质、蛋白质和激素,如生物胺和肽,以及 microRNAs (miRNAs)。LDCVs 的分离对于包括囊泡融合、囊泡酸化、单胺转运和 LDCVs 中储存的 miRNAs 在内的功能研究至关重要。尽管已经报道了几种分离 LDCVs 的方法,但最终的馏分仍然严重受到其他细胞器的污染,从而影响生物化学特征。在这里,我们从牛肾上腺髓质中以高产量和高纯度分离出 LDCVs(嗜铬粒)。该分级方案结合了差速和连续蔗糖梯度离心,可减少线粒体等主要污染物。纯化的 LDCVs 显示出由内源性 V-ATPase 引起的强大酸化,并与人工膜进行 SNARE 介导的融合。有趣的是,LDCVs 含有特定的 miRNAs,如 miR-375,miR-375 被蛋白质复合物稳定,可抵抗 RNase A。该方案可用于研究 LDCVs 的生物学功能。