Depletion of Myeloid Cells Exacerbates Hepatitis and Induces an Aberrant Increase in Histone H3 in Mouse Serum
Depletion of Myeloid Cells Exacerbates Hepatitis and Induces an Aberrant Increase in Histone H3 in Mouse Serum
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DOI：
10.1002/hep.28878
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发表时间：
2017-01-01
期刊：
影响因子：
13.5
通讯作者：
Nakano, Hiroyasu
中科院分区：
文献类型：
--
作者：
Piao, Xuehua;Yamazaki, Soh;Nakano, Hiroyasu
Tissue-resident macrophages and bone marrow (BM)-derived monocytes play a crucial role in the maintenance of tissue homeostasis; however, their contribution to recovery from acute tissue injury is not fully understood. To address this issue, we generated an acute murine liver injury model using hepatocyte-specific Cflar-deficient (Cflar(Hep-low)) mice. Cellular FLICE-inhibitory protein expression was down-regulated in Cflar-deficient hepatocytes, which thereby increased susceptibility of hepatocytes to death receptor-induced apoptosis. Cflar(Hep-low) mice developed acute hepatitis and recovered with clearance of apoptotic hepatocytes at 24 hours after injection of low doses of tumor necrosis factor a (TNF alpha), which could not induce hepatitis in wild-type (WT) mice. Depletion of Kupffer cells (KCs) by clodronate liposomes did not impair clearance of dying hepatocytes or exacerbate hepatitis in Cflar(Hep-low) mice. To elucidate the roles of BM-derived monocytes and neutrophils in clearance of apoptotic hepatocytes, we examined the effect of depletion of these cells on TNF alpha-induced hepatitis in Cflar(Hep-low) mice. We reconstituted Cflar(Hep-low) mice with BM cells from transgenic mice in which human diphtheria toxin receptor (DTR) was expressed under control of the lysozyme M (LysM) promoter. TNF alpha-induced infiltration of myeloid cells, including monocytes and neutrophils, was completely ablated in LysM-DTR BM-reconstituted Cflar(Hep-low) mice pretreated with diphtheria toxin, whereas KCs remained present in the livers. Under these experimental conditions, LysM-DTR BM-reconstituted Cflar(Hep-low) mice rapidly developed severe hepatitis and succumbed within several hours of TNF alpha injection. We found that serum interleukin-6 (IL-6), TNF alpha, and histone H3 were aberrantly increased in LysM-DTR BM-reconstituted, but not in WT BM-reconstituted, Cflar(Hep-low) mice following TNF alpha injection. Conclusion: These findings indicate an unexpected role of myeloid cells in decreasing serum IL-6, TNF alpha, and histone H3 levels via the suppression of TNF alpha-induced hepatocyte apoptosis.
