Departamento de Clínica e Cirurgia Veterinárias, Escola de Veterinária, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Department of Medical Microbiology and Immunology, University of California, Davis, California, USA.
mBio. 2024 Mar 13;15(3):e0325223. doi: 10.1128/mbio.03252-23. Epub 2024 Jan 30.
Pericytes are located around blood vessels, in close contact with endothelial cells. We discovered that pericytes dampen pro-inflammatory endothelial cell responses. Endothelial cells co-cultured with pericytes had markedly reduced expression of adhesion molecules (PECAM-1 and ICAM-1) and proinflammatory cytokines (CCL-2 and IL-6) in response to bacterial stimuli (, , or lipopolysaccharide). Pericyte-depleted mice intraperitoneally inoculated with either , a stealthy pathogen that does not trigger detectable inflammation, or , developed peritonitis. Further, during infection, pericyte-depleted mice developed severe intestinal inflammation, which was not evident in control mice. The anti-inflammatory effect of pericytes required connexin 43, as either chemical inhibition or silencing of connexin 43 abrogated pericyte-mediated suppression of endothelial inflammatory responses. Our results define a mechanism by which pericytes modulate inflammation during infection, which shifts our understanding of pericyte biology: from a structural cell to a pro-active player in modulating inflammation.
A previously unknown mechanism by which pericytes modulate inflammation was discovered. The absence of pericytes or blocking interaction between pericytes and endothelium through connexin 43 results in stronger inflammation, which shifts our understanding of pericyte biology, from a structural cell to a player in controlling inflammation.
周细胞位于血管周围,与内皮细胞密切接触。我们发现周细胞能抑制内皮细胞的促炎反应。与周细胞共培养的内皮细胞在受到细菌刺激( 、 或 脂多糖)时,黏附分子(PECAM-1 和 ICAM-1)和促炎细胞因子(CCL-2 和 IL-6)的表达明显降低。用周细胞耗竭小鼠经腹腔接种 ,一种不会引发可检测到的炎症的隐匿病原体,或 ,发展为腹膜炎。此外,在 感染期间,周细胞耗竭小鼠发生严重的肠道炎症,而在对照小鼠中则不明显。周细胞的抗炎作用需要连接蛋白 43,因为化学抑制或沉默连接蛋白 43 均可消除周细胞对内皮炎症反应的抑制作用。我们的研究结果定义了周细胞在感染过程中调节炎症的一种机制,这改变了我们对周细胞生物学的理解:从一种结构细胞转变为调节炎症的积极参与者。
发现了一种以前未知的周细胞调节炎症的机制。周细胞缺失或通过连接蛋白 43 阻断周细胞与内皮细胞的相互作用,导致炎症加剧,这改变了我们对周细胞生物学的理解,即从一种结构细胞转变为控制炎症的参与者。