Lipid body formation during maturation of human mast cells

被引:35
作者
Dichlberger, Andrea [1 ]
Schlager, Stefanie [1 ]
Lappalainen, Jani [1 ]
Kakela, Reijo [2 ]
Hattula, Katarina [3 ]
Butcher, Sarah J. [3 ]
Schneider, Wolfgang J. [4 ]
Kovanen, Petri T. [1 ]
机构
[1] Wihuri Res Inst, FIN-00140 Helsinki, Finland
[2] Univ Helsinki, Dept Biosci, FIN-00014 Helsinki, Finland
[3] Univ Helsinki, Inst Biotechnol, FIN-00014 Helsinki, Finland
[4] Med Univ Vienna, Dept Med Biochem, A-1030 Vienna, Austria
基金
芬兰科学院; 奥地利科学基金会;
关键词
arachidonic acid; eicosanoids; fatty acid; inflammation; perilipin; secretory granules; triacylglycerol; INFLAMMATORY CELLS; PERIPHERAL-BLOOD; IN-VITRO; BODIES; DROPLETS; ADIPOPHILIN; PURIFICATION; MACROPHAGES; ADIPOCYTES; ACTIVATION;
D O I
10.1194/jlr.M019737
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipid droplets, also called lipid bodies (LB) in inflammatory cells, are important cytoplasmic organelles. However, little is known about the molecular characteristics and functions of LBs in human mast cells (MC). Here, we have analyzed the genesis and components of LBs during differentiation of human peripheral blood-derived CD34(+) progenitors into connective tissue-type MCs. In our serum-free culture system, the maturing MCs, derived from 18 different donors, invariably developed triacylglycerol (TG)-rich LBs. Not known heretofore, the MCs transcribe the genes for perilipins (PLIN) 1-4, but not PLIN5, and PLIN2 and PLIN3 display different degrees of LB association. Upon MC activation and ensuing degranulation, the LBs were not cosecreted with the cytoplasmic secretory granules. Exogenous arachidonic acid (AA) enhanced LB genesis in Triacsin C-sensitive fashion, and it was found to be preferentially incorporated into the TGs of LBs. The large TG-associated pool of AA in LBs likely is a major precursor for eicosanoid production by MCs. In summary, we demonstrate that cultured human MCs derived from CD34(+) progenitors in peripheral blood provide a new tool to study regulatory mechanisms involving LB functions, with particular emphasis on AA metabolism, eicosanoid biosynthesis, and subsequent release of proinflammatory lipid mediators from these cells.-Dichlberger, A., S. Schlager, J. Lappalainen, R. Kakela, K. Hattula, S. J. Butcher, W. J. Schneider, and P. T. Kovanen. Lipid body formation during maturation of human mast cells. J. Lipid Res. 2011. 52: 2198-2208.
引用
收藏
页码:2198 / 2208
页数:11
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