Shao Wen-Hai, Zhen Yuxuan, Eisenberg Robert A, Cohen Philip L
Department of Medicine, Division of Rheumatology, Temple University, Philadelphia, PA 19140, USA.
Clin Immunol. 2009 Oct;133(1):138-44. doi: 10.1016/j.clim.2009.06.002. Epub 2009 Jul 24.
The Mer receptor tyrosine kinase is both an important mediator of apoptotic cell phagocytosis and a regulator of macrophage and DC cytokine production. Since phenotypically distinguishable macrophages are known to have different functions, we have examined Mer expression of murine splenic macrophages. We also used serum deficient in the Mer ligand, growth arrest-specific protein 6 (Gas6) to define better the role of this Mer ligand in macrophage function. By immunofluorescence staining, we found Mer to be strongly expressed in splenic red pulp, largely on platelets. We also found Mer expression on marginal zone macrophages. Strikingly, all tingible body macrophages bore Mer. In functional phagocytosis assays of apoptotic cells, Gas6 appeared to be the sole ligand for Mer, and this system accounted for about 30% of splenic macrophage phagocytosis of apoptotic cells. Taken together, the expression pattern of Mer on macrophage subpopulations in the spleen and its Gas6-dependent role in macrophage phagocytosis suggest an important role for Mer in the modulation of immune responses.
Mer受体酪氨酸激酶既是凋亡细胞吞噬作用的重要介质,也是巨噬细胞和树突状细胞细胞因子产生的调节因子。由于已知表型可区分的巨噬细胞具有不同功能,我们检测了小鼠脾脏巨噬细胞的Mer表达。我们还使用缺乏Mer配体生长停滞特异性蛋白6(Gas6)的血清,以更好地确定这种Mer配体在巨噬细胞功能中的作用。通过免疫荧光染色,我们发现Mer在脾脏红髓中大量表达,主要位于血小板上。我们还在边缘区巨噬细胞上发现了Mer表达。令人惊讶的是,所有可染小体巨噬细胞都带有Mer。在凋亡细胞的功能性吞噬试验中,Gas6似乎是Mer的唯一配体,并且该系统约占脾脏巨噬细胞对凋亡细胞吞噬作用的30%。综上所述,Mer在脾脏巨噬细胞亚群上的表达模式及其在巨噬细胞吞噬作用中依赖Gas6的作用表明Mer在免疫反应调节中具有重要作用。