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首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Monocyte and plasma expression of TAM ligand and receptor in renal failure: Links to unregulated immunity and chronic inflammation
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Monocyte and plasma expression of TAM ligand and receptor in renal failure: Links to unregulated immunity and chronic inflammation

机译:TAM配体和受体在肾衰竭中的单核细胞和血浆表达:与免疫失调和慢性炎症的联系

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摘要

Chronic inflammation is increased in patients with chronic kidney disease (CKD) and contributes to cardiovascular morbidity and mortality. Specific immune mechanisms and pathways that drive and maintain chronic inflammation in CKD are not well described. The TAM ligands (Gas6 and protein S) and receptors (Axl and Mer) have been recently recognized as playing a prominent role in immune regulation. The receptors exist in both soluble and cell-bound forms; the soluble receptors (sAxl and sMer) are believed to compete with the bound receptors and thus inhibit their function. In this study, we determined the expression of cell-bound and soluble TAM proteins in patients with CKD. CKD patients had significantly lower expression of Mer in monocytes, yet increased expression of soluble TAM receptors sAxl and sMer in plasma compared to controls. The metalloproteinase ADAM 17, responsible for cleavage of Mer to its soluble form, was increased in patient monocytes. Elevated levels of soluble TAM receptors were more evident in patients with progressive renal failure. These observations suggest that functional deficiency of TAM receptor-mediated regulation of inflammation may contribute to chronic inflammation in patients with CKD. (C) 2015 Elsevier Inc. All rights reserved.
机译:患有慢性肾脏疾病(CKD)的患者的慢性炎症会增加,并会增加心血管疾病的发病率和死亡率。尚未很好描述驱动和维持CKD慢性炎症的特定免疫机制和途径。 TAM配体(Gas6和蛋白S)和受体(Axl和Mer)最近在免疫调节中起着重要作用。受体以可溶性和细胞结合形式存在。据信可溶性受体(sAxl和sMer)与结合的受体竞争,因此抑制了它们的功能。在这项研究中,我们确定了细胞结合和可溶性TAM蛋白在CKD患者中的表达。与对照组相比,CKD患者的单核细胞中Mer的表达明显降低,而血浆中可溶性TAM受体sAxl和sMer的表达却增加。患者单核细胞中负责将Mer裂解为可溶形式的金属蛋白酶ADAM 17增加。进行性肾衰竭患者中可溶性TAM受体水平升高更为明显。这些观察结果提示,TAM受体介导的炎症调节功能缺失可能导致CKD患者的慢性炎症。 (C)2015 Elsevier Inc.保留所有权利。

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