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糖尿病视网膜病变中周细胞和血管平滑肌细胞的胞葬作用受损。

Impaired Efferocytosis of Pericytes and Vascular Smooth Muscle Cells in Diabetic Retinopathy.

作者信息

Gardiner Tom A, Little Karis, Stitt Alan W

机构信息

School of Medicine, Dentistry & Biomedical Sciences, Queen's University Belfast, Belfast BT9 7BL, UK.

Centre for Experimental Medicine, Queen's University Belfast, Belfast BT9 7BL, UK.

出版信息

Cells. 2025 Aug 30;14(17):1349. doi: 10.3390/cells14171349.

Abstract

During diabetic retinopathy (DR), cell death has been characterized in all of the major retinal cell types, but was observed initially in the microvasculature, particularly the mural cells: pericytes and vascular smooth muscle cells (VSMCs). Indeed, our ability to identify the mural cell corpses called "ghost cells" within the vascular basement membranes (BMs) in eyes of diabetic patients and animal models is indicative that removal of dead cells, or efferocytosis (EF), is dysfunctional during this disease. EF is the process whereby apoptotic cells are eliminated through phagocytic engulfment and digestion and is essential to maintain tissue integrity and immune homeostasis. The process occurs in three distinct phases: finding and recognition, engulfment, and digestion, under the direction of "find me" and "eat me" signals and a large array of their cognate receptors and bridging molecules. Efferocytosis can be performed by many cell types, but most efficiently by professional phagocytes, and with such rapidity that the process is extremely difficult to detect in healthy tissues. As delayed EF is a recognized cause of autoimmune and inflammatory disease, mural cell death in DR may create inflammatory foci in the neurovascular unit (NVU). Here we discuss the basic mechanisms of EF in the context of DR and the impact of diabetic metainflammation on EF effector cell dysfunction.

摘要

在糖尿病视网膜病变(DR)过程中,所有主要视网膜细胞类型均出现细胞死亡,但最初是在微血管系统中观察到的,尤其是壁细胞:周细胞和血管平滑肌细胞(VSMC)。事实上,我们能够在糖尿病患者和动物模型的眼睛血管基底膜(BM)内识别出称为“幽灵细胞”的壁细胞尸体,这表明在这种疾病中,死细胞的清除,即胞葬作用(EF)功能失调。EF是通过吞噬性吞噬和消化来清除凋亡细胞的过程,对于维持组织完整性和免疫稳态至关重要。该过程在“找到我”和“吃掉我”信号以及大量同源受体和桥接分子的指导下,分三个不同阶段进行:寻找与识别、吞噬和消化。胞葬作用可由多种细胞类型执行,但最有效的是专业吞噬细胞,其速度极快,以至于在健康组织中极难检测到该过程。由于延迟的EF是自身免疫和炎症性疾病的公认原因,DR中的壁细胞死亡可能会在神经血管单元(NVU)中产生炎症灶。在此,我们讨论DR背景下EF的基本机制以及糖尿病元炎症对EF效应细胞功能障碍的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e79/12428674/7ca814b1022d/cells-14-01349-g001.jpg

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