巨噬细胞
伤口愈合
免疫染色
M2巨噬细胞
表型
医学
免疫学
病理生理学
病理
免疫组织化学
生物
体外
生物化学
基因
作者
Mingyuan Miao,Yiwen Niu,Ting Xie,Bo Yuan,Chun Qing,Shuliang Lu
标识
DOI:10.1111/j.1524-475x.2012.00772.x
摘要
Abstract Macrophages play a critical role in wound healing and can be activated to two distinctive phenotypes in vitro: classical macrophage activation ( caM ) and alternative macrophage activation ( aaM ). This study investigated whether the impaired cutaneous repair observed in streptozotocin‐induced diabetic rats was associated with altered macrophage activation. Our results show that macrophage activation phenotypes could be observed in wound healing through double immunostaining. The caM macrophages appeared in the initial stage of wound healing, followed by aaM macrophages, which predominated in normal wounds. However, through examining markers associated with activation by immunoblotting and real‐time polymerase chain reaction ( PCR ), diabetic wounds demonstrated insufficient caM in the early stage but excessive aaM in the later proliferative phase. Moreover, the macrophage activation markers were correlated with the instructive T helper cell type 1 ( Th1 )/ Th2 cytokines in both groups. It was indicated that changed macrophage activation might contribute to impaired healing in diabetes wounds, and that strategies for reverting this abnormal activation could be useful for enhancing the wound healing process.
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