Phosphatidylserine directly and positively regulates fusion of myoblasts into myotubes

被引:61
作者
Jeong, Jaemin [1 ,2 ]
Conboy, Irina M. [1 ]
机构
[1] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[2] Korea Inst Radiol & Med Sci, Div Radiat Canc Res, Seoul, South Korea
关键词
Phosphatidylserine; Myoblast; Myotube; Fusion; Liposome; Annexin V; STEM/PRECURSOR CELLS; IN-VITRO; MUSCLE; EXPRESSION; MACROPHAGES; MEMBRANES;
D O I
10.1016/j.bbrc.2011.08.128
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Cell membrane consists of various lipids such as phosphatidylserine (PS), phosphatidylcholine (PC), and phosphatidylethanolamine (PE). Among them, PS is a molecular marker of apoptosis, because it is located to the inner leaflet of plasma membrane generally but it is moved to the outer leaflet during programmed cell death. The process of apoptosis has been implicated in the fusion of muscle progenitor cells, myoblasts, into myotubes. However, it remained unclear whether PS regulates muscle cell differentiation directly. In this paper, localization of PS to the outer leaflet of plasma membrane in proliferating primary myoblasts and during fusion of these myoblasts into myotubes is validated using Annexin V. Moreover, we show the presence of PS clusters at the cell-cell contact points, suggesting the importance of membrane ruffling and PS exposure for the myogenic cell fusion. Confirming this conclusion, experimentally constructed PS, but not PC liposomes dramatically enhance the formation of myotubes from myoblasts, thus demonstrating a direct positive effect of PS on the muscle cell fusion. In contrast, myoblasts exposed to PC liposomes produce long myotubes with low numbers of myonuclei. Moreover, pharmacological masking of PS on the myoblast surface inhibits fusion of these cells into myotubes in a dose-dependent manner. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:9 / 13
页数:5
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