炎症
纤维化
肾脏疾病
肾
分子医学
巨噬细胞极化
巨噬细胞
生物
免疫学
表型
病理
癌症研究
医学
细胞凋亡
细胞周期
体外
内分泌学
遗传学
基因
作者
Ji Zeng,Yuan Zhang,Cheng Huang
出处
期刊:Molecular Medicine Reports
[Spandidos Publications]
日期:2023-12-20
卷期号:29 (2)
被引量:7
标识
DOI:10.3892/mmr.2023.13152
摘要
Chronic kidney disease (CKD) is a significant public health concern. Renal fibrosis is the final common pathway in the progression of kidney diseases, irrespective of the initial injury. Substantial evidence underscores the pivotal role of renal inflammation in the genesis of renal fibrosis. The presence of macrophages within normal renal tissue is significantly increased within diseased renal tissue, indicative of their crucial regulatory function in inflammation and fibrosis. Macrophages manifest a high degree of heterogeneity, exhibiting distinct phenotypic and functional traits in response to diverse stimuli within the local microenvironment in various types of kidney diseases. Broadly, macrophages are categorized into two principal groups: Classically activated, designated as M1 macrophages and alternatively activated, designated as M2 macrophages. A number of experimental models are widely used to study the underlying mechanisms driving renal inflammation and fibrosis progression. The present review delineated the phenotypic and functional attributes of macrophages present in diverse induced models, analyzing their disposition in relation to M1 and M2 polarization states.
科研通智能强力驱动
Strongly Powered by AbleSci AI