CCR2型
渗透(HVAC)
纤维化
MAPK/ERK通路
巨噬细胞
医学
细胞生物学
癌症研究
炎症
生物
信号转导
免疫学
病理
趋化因子
材料科学
生物化学
趋化因子受体
复合材料
体外
作者
Jinpeng Sun,Mohan Shi,Zeyuan Song,Hua Feng,Xiyun Yan,Mingshun Zhang,Hongxia Duan,Jun Liu
标识
DOI:10.1016/j.intimp.2024.112528
摘要
Low back pain due to epidural fibrosis is a major complication after spine surgery. Macrophages infiltrate the wound area post laminectomy, but the role of macrophages in epidural fibrosis remains largely elusive. In a mouse model of laminectomy, macrophage depletion decreased epidural fibrosis. CD146, an adhesion molecule involved in cell migration, is expressed by macrophages. CD146-defective macrophages exhibited impaired migration, which was mediated by reduced expression of CCR2 and suppression of the MAPK/ERK signaling pathway. CD146-defective macrophages suppress the MAPK/ERK signaling pathway by increasing Erdr1. In vivo, CD146 deficiency decreased macrophage infiltration and reduced extracellular matrix deposition in wound tissues. Moreover, the anti-CD146 antibody AA98 suppressed macrophage infiltration and epidural fibrosis. Taken together, these findings demonstrated that CD146 deficiency alleviates epidural fibrosis by decreasing the migration of macrophages via the Erdr1/ERK/CCR2 pathway. Blocking CD146 and macrophage infiltration may help alleviate epidural fibrosis.
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