Zahr Tarik, Sun Kevin, Qiang Li
Naomi Berrie Diabetes Center, Columbia University, New York, NY, USA.
Department of Molecular Pharmacology and Therapeutics, Columbia University, New York, NY, USA.
Med Rev (2021). 2022 Sep 20;2(4):324-327. doi: 10.1515/mr-2022-0023. eCollection 2022 Aug.
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.
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,库普弗细胞就会展现出独特的细胞机制,具备长寿和自我更新能力,使其成为促进肝内有效通讯的关键参与者。然而,在非酒精性脂肪性肝炎(NASH)等疾病状态下,这种情况会受到损害,此时会观察到胚胎来源的库普弗细胞(EmKCs)的丢失。尽管如此,其他类似库普弗细胞和源自库普弗细胞的细胞群体开始形成,并在NASH发病机制中发挥多种作用,通常呈现出与NASH相关的分子特征。在此,我们简要概述近期描述肝脏中库普弗细胞极化和重编程的报告。我们描述了库普弗细胞细胞身份的复杂性、它们重编程为成纤维细胞样和内皮细胞样细胞的推测能力,以及在NASH中的潜在影响。