Characterization of Vesicles Secreted from Insulinoma NIT-1 Cells

被引:48
作者
Lee, Hyo Sun
Jeong, Jaeho
Lee, Kong-Joo [1 ]
机构
[1] Ewha Womans Univ, Coll Pharm, Ctr Cell Signaling & Drug Discovery Res, Seoul 120750, South Korea
关键词
proteomic analysis; pancreatic beta cells; insulinoma; secreted vesicles; calcium; tandem mass spectrometry; post-translational modifications; TANDEM MASS-SPECTROMETRY; PROTEOMIC ANALYSIS; POSTTRANSLATIONAL MODIFICATIONS; EXOSOMES; PROTEINS; IDENTIFICATION; EXOCYTOSIS; MICROVESICLES; INDUCTION; RECEPTOR;
D O I
10.1021/pr900009y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Insulinoma NIT-1, an insulin-secreting mouse cell line, secretes vesicles in response to glucose or calcium. These vesicles, like exosomes, are relatively homogeneous (30-100 nm). We analyzed their protein profiles employing one-dimensional SDS gel electrophoresis combined with nanoLC-ESI-qTOF tandem mass spectrometry, and searched for post-translational modifications (PTMs) using MOD! algorithm. We identified 270 proteins which matched at least two peptides reproducibly in duplicate runs. These proteins included metabolic proteins, endocytosis/exocytosis related proteins, chaperones, cytoskeletal proteins, membrane transporters/ion channels, signaling molecules, and nucleic acid binding proteins. Over 200 of these are newly identified proteins for the first time in secreted vesicles, and included RNA- and translation-related proteins, ubiquitin- and protein-degradation related proteins and post-translationally modified proteins. The rest of the proteins identified in this study were similar to those reported by others to be present in exosomes of various origins. The present study demonstrates that vesicles secreted from insulinoma NIT-1 cells have some properties, common to exosomes from lymphocytes and cancer cells, and some differing from those of other types of exosomes. We believe that the modified and newly identified proteins we identified in secreted vesicles from insulinoma NIT-1 cells have the potential to provide insights into mechanisms of biogenesis and function of secreted vesicles and may help explain the impairment of insulin secretion in islets from type-2 diabetes.
引用
收藏
页码:2851 / 2862
页数:12
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