Constitutive Neutrophil Apoptosis: Regulation by Cell Concentration via S100 A8/9 and the MEK - ERK Pathway

被引:33
作者
Atallah, Mizhir [1 ]
Krispin, Alon [1 ]
Trahtemberg, Uriel [1 ]
Ben-Hamron, Sandrine [1 ]
Grau, Amir [1 ]
Verbovetski, Inna [1 ]
Mevorach, Dror [1 ]
机构
[1] Hadassah Hebrew Univ, Med Ctr Jerusalem, Rheumatol Res Ctr, Lab Cellular & Mol Immunol,Dept Med, Jerusalem, Israel
关键词
BONE-MARROW; FAS LIGAND; PHOSPHATIDYLINOSITOL; 3-KINASE; DIFFERENTIAL EXPRESSION; RHEUMATOID-ARTHRITIS; GM-CSF; DEATH; SURVIVAL; CYTOKINES; INFLAMMATION;
D O I
10.1371/journal.pone.0029333
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Programmed cell death (PCD) is a fundamental mechanism in tissue and cell homeostasis. It was long suggested that apoptosis regulates the cell number in diverse cell populations; however no clear mechanism was shown. Neutrophils are the short-lived, first-line defense of innate immunity, with an estimated t = 1/2 of 8 hours and a high turnover rate. Here we first show that spontaneous neutrophil constitutive PCD is regulated by cell concentrations. Using a proteomic approach, we identified the S100 A8/9 complex, which constitutes roughly 40% of cytosolic protein in neutrophils, as mediating this effect. We further demonstrate that it regulates cell survival via a signaling mechanism involving MEK-ERK via TLR4 and CD11B/CD18. This mechanism is suggested to have a fine-tuning role in regulating the neutrophil number in bone marrow, peripheral blood, and inflammatory sites.
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页数:11
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