Su Heng, McClarty Grant, Dong Feng, Hatch Grant M, Pan Zhixing K, Zhong Guangming
Department of Microbiology and Immunology, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229, USA.
J Biol Chem. 2004 Mar 5;279(10):9409-16. doi: 10.1074/jbc.M312008200. Epub 2003 Dec 15.
Chlamydiae, a diverse group of obligate intracellular pathogens replicating within cytoplasmic vacuoles of eukaryotic cells, are able to acquire lipids from host cells. Here we report that activation of the host Raf-MEK-ERK-cPLA2 signaling cascade is required for the chlamydial uptake of host glycerophospholipids. Both the MAP kinase pathway (Ras/Raf/MEK/ERK) and Ca(2+)-dependent cytosolic phospholipase A2 (cPLA2) were activated in chlamydia-infected cells. The inhibition of cPLA2 activity resulted in the blockade of the chlamydial uptake of host glycerophospholipids and impairment in chlamydial growth. Blocking either c-Raf-1 or MEK1/2 activity prevented the chlamydial activation of ERK1/2, leading to the suppression of both chlamydial activation of the host cPLA2 and uptake of glycerophospholipids from the host cells. The chlamydia-induced phosphorylation of cPLA2 was also blocked by a dominant negative ERK2. Furthermore, activation of both ERK1/2 and cPLA2 was dependent on chlamydial growth and restricted within chlamydia-infected cells, suggesting an active manipulation of the host ERK-cPLA2 signaling pathway by chlamydiae.
衣原体是一类多样的专性细胞内病原体,在真核细胞的胞质空泡内复制,能够从宿主细胞获取脂质。在此我们报告,宿主Raf-MEK-ERK-cPLA2信号级联的激活是衣原体摄取宿主甘油磷脂所必需的。在衣原体感染的细胞中,丝裂原活化蛋白激酶途径(Ras/Raf/MEK/ERK)和钙依赖性胞质磷脂酶A2(cPLA2)均被激活。抑制cPLA2活性导致衣原体摄取宿主甘油磷脂受阻,衣原体生长受损。阻断c-Raf-1或MEK1/2活性可阻止衣原体对ERK1/2的激活,从而抑制宿主cPLA2的衣原体激活以及从宿主细胞摄取甘油磷脂。显性负性ERK2也可阻断衣原体诱导的cPLA2磷酸化。此外,ERK1/2和cPLA2的激活均依赖于衣原体的生长,且局限于衣原体感染的细胞内,提示衣原体对宿主ERK-cPLA2信号通路进行了主动操控。