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组成性中性粒细胞凋亡:通过 S100A8/9 和 MEK-ERK 通路调节细胞浓度。

Constitutive neutrophil apoptosis: regulation by cell concentration via S100 A8/9 and the MEK-ERK pathway.

机构信息

The Laboratory for Cellular and Molecular Immunology, Department of Medicine, Hadassah-Hebrew University Medical Center Jerusalem, Jerusalem, Israel.

出版信息

PLoS One. 2012;7(2):e29333. doi: 10.1371/journal.pone.0029333. Epub 2012 Feb 17.

Abstract

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.

摘要

程序性细胞死亡(PCD)是组织和细胞动态平衡的基本机制。长期以来,人们一直认为细胞凋亡调节着各种细胞群中的细胞数量;然而,并没有明确的机制被揭示。中性粒细胞是先天免疫的短暂的一线防御细胞,半衰期估计为 8 小时的 1/2,且周转率很高。在这里,我们首先表明,自发的中性粒细胞组成性 PCD 受细胞浓度的调节。通过蛋白质组学方法,我们鉴定出 S100A8/9 复合物,它构成了中性粒细胞胞质蛋白的大约 40%,介导了这种作用。我们进一步证明,它通过涉及 TLR4 和 CD11B/CD18 的 MEK-ERK 的信号机制来调节细胞存活。该机制被认为在调节骨髓、外周血和炎症部位中性粒细胞数量方面具有微调作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb2e/3281816/8ee0e8bbcc47/pone.0029333.g001.jpg

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