Holm A, Tejle K, Gunnarsson T, Magnusson K-E, Descoteaux A, Rasmusson B
Division of Medical Microbiology, Department of Molecular and Clinical Medicine, Faculty of Health Sciences, Linköping University, S-581 85 Linköping, Sweden.
Biochem Biophys Res Commun. 2003 Mar 21;302(4):653-8. doi: 10.1016/s0006-291x(03)00231-6.
Protein kinase C alpha (PKC alpha) participates in F-actin remodeling during phagocytosis and phagosomal maturation in macrophages. Leishmania donovani promastigotes, which inhibit phagosomal maturation, cause accumulation of periphagosomal F-actin instead of the disassembly observed around other prey [Cell. Microbiol. 7 (2001) 439]. This accumulation is induced by promastigote lipophosphoglycan (LPG), which has several effects on macrophages including inhibition of PKC alpha. To investigate a possible connection between PKC alpha and LPG's effects on actin dynamics, we utilized RAW264.7 macrophages overexpressing dominant-negative PCK alpha (DN PKC alpha). We found increased cortical F-actin and decreased phagocytic capacity, as well as defective periphagosomal F-actin breakdown and inhibited phagosomal maturation in the DN PKC alpha-overexpressing cells, effects similar to those seen in controls subjected to LPG-coated prey. The results indicate that PKC alpha is involved in F-actin turnover in macrophages and that PKC alpha-dependent breakdown of periphagosomal F-actin is required for phagosomal maturation, and endorse the hypothesis that intracellular survival of L. donovani involves inhibition of PKC alpha by LPG.
蛋白激酶Cα(PKCα)参与巨噬细胞吞噬作用和吞噬体成熟过程中的F-肌动蛋白重塑。杜氏利什曼原虫前鞭毛体可抑制吞噬体成熟,导致吞噬体周围F-肌动蛋白积累,而不是像其他猎物周围那样发生解聚[《细胞微生物学》7(2001)439]。这种积累是由前鞭毛体脂磷壁酸(LPG)诱导的,LPG对巨噬细胞有多种作用,包括抑制PKCα。为了研究PKCα与LPG对肌动蛋白动力学影响之间的可能联系,我们利用了过表达显性负性PCKα(DN PKCα)的RAW264.7巨噬细胞。我们发现,在过表达DN PKCα的细胞中,皮质F-肌动蛋白增加,吞噬能力下降,吞噬体周围F-肌动蛋白分解缺陷,吞噬体成熟受到抑制,这些效应与用LPG包被的猎物处理的对照中观察到的效应相似。结果表明,PKCα参与巨噬细胞中F-肌动蛋白的周转,吞噬体成熟需要PKCα依赖的吞噬体周围F-肌动蛋白分解,并支持杜氏利什曼原虫细胞内存活涉及LPG抑制PKCα的假说。