Isolation of large dense-core vesicles from bovine adrenal medulla for functional studies

被引:15
作者
Birinci, Yelda [1 ]
Preobraschenski, Julia [2 ]
Ganzella, Marcelo [2 ]
Jahn, Reinhard [2 ]
Park, Yongsoo [1 ,3 ]
机构
[1] Koc Univ, Dept Mol Biol & Genet, Istanbul 34450, Turkey
[2] Max Planck Inst Biophys Chem, Dept Neurobiol, Fassberg 11, Gottingen 37077, Germany
[3] Hamad Bin Khalifa Univ, Qatar Fdn, QBRI, Neurol Disorders Res Ctr, POB 34110, Doha, Qatar
关键词
MEMBRANE; EXOCYTOSIS; GRANULE; MODEL; ACID;
D O I
10.1038/s41598-020-64486-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:8
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