Reglero-Real Natalia, Rolas Loïc, Nourshargh Sussan
Departamento de Biología Molecular, Instituto Universitario de Biología Molecular (IUBM) and Centro de Biología Molecular Severo Ochoa (CBM), Universidad Autónoma de Madrid, UAM-CSIC, Madrid, Spain.
Instituto de Investigación Sanitaria La Princesa , Madrid, Spain.
J Exp Med. 2025 Jul 7;222(7). doi: 10.1084/jem.20242154. Epub 2025 Jun 2.
Leukocyte recruitment to sites of inflammation is vital for orchestrating an effective immune response. Key to this process is the ability of leukocytes to migrate through venular walls, engaging in sequential interactions with endothelial cells, pericytes, and the venular basement membrane. The aging process exerts profound effects on the molecular and functional properties of the vasculature, thereby influencing the profile and dynamics of leukocyte trafficking during inflammation. In this review, by focusing mainly on neutrophils, we summarize key examples of how the aged microvasculature and perivascular stroma cells promote dysregulated leukocyte-venular wall interactions and present the associated molecular mechanisms. Additionally, we discuss the functional implications of such aberrant leukocyte behavior to age-related and chronic inflammatory pathologies.
白细胞募集到炎症部位对于协调有效的免疫反应至关重要。这一过程的关键在于白细胞穿过小静脉壁的能力,即与内皮细胞、周细胞和小静脉基底膜进行一系列相互作用。衰老过程对脉管系统的分子和功能特性产生深远影响,从而影响炎症期间白细胞运输的特征和动态。在本综述中,我们主要聚焦于中性粒细胞,总结老年微血管和血管周围基质细胞如何促进白细胞与小静脉壁相互作用失调的关键实例,并介绍相关分子机制。此外,我们还讨论了这种异常白细胞行为对与年龄相关的慢性炎症病理的功能影响。