Kupffer细胞在非酒精性脂肪性肝炎中的可极化和可重编程特性。

Medical review (Berlin, Germany) Pub Date : 2022-09-20 eCollection Date: 2022-08-01 DOI:10.1515/mr-2022-0023
Tarik Zahr, Kevin Sun, Li Qiang
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引用次数: 0

摘要

库普弗细胞(KCs)是肝脏中的常驻巨噬细胞,其起源与骨髓来源的巨噬细胞相似。一旦分化,KCs表现出独特的细胞机制,能够长寿和自我更新,使其成为促进有效肝内交流的关键因素。然而,在非酒精性脂肪性肝炎(NASH)等疾病状态下,这一点会受到影响,在这种情况下,可以观察到胚胎来源的KCs(EmKCs)的损失。尽管如此,其他KC样和KC衍生的群体开始形成,并在NASH发病机制中发挥各种作用,通常采用NASH相关的分子特征。在这里,我们简要概述了最近关于肝脏KC极化和重编程的报道。我们描述了KC细胞身份的复杂性,他们提出的重新编程为成纤维细胞样和内皮细胞样细胞的能力,以及在NASH中的潜在意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The polarizable and reprogrammable identity of Kupffer cells in Nonalcoholic Steatohepatitis.

The polarizable and reprogrammable identity of Kupffer cells in Nonalcoholic Steatohepatitis.

Kupffer cells (KCs) are the resident macrophages of the liver with similar origins to myeloid-derived macrophages. Once differentiated, KCs exhibit distinct cellular machinery capable of longevity and self-renewal, making them a crucial player in promoting effective intrahepatic communication. However, this gets compromised in disease states like Nonalcoholic Steatohepatitis (NASH), where the loss of embryo-derived KCs (EmKCs) is observed. Despite this, other KC-like and KC-derived populations start to form and contribute to a variety of roles in NASH pathogenesis, often adopting a NASH-associated molecular signature. Here we offer a brief overview of recent reports describing KC polarization and reprogramming in the liver. We describe the complexities of KC cellular identity, their proposed ability to reprogram to fibroblast-like and endothelial-like cells, and the potential implications in NASH.

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