TLR9型
糖尿病肾病
TLR2型
内分泌学
内科学
骨髓
炎症
发病机制
肿瘤坏死因子α
肾
生物
医学
TLR4型
基因表达
生物化学
基因
DNA甲基化
作者
Seigo Ito,Hiroyuki Nakashima,Takuya Ishikiriyama,Masahiro Nakashima,Akira Yamagata,Toshihiko Imakiire,Manabu Kinoshita,Shuhji Seki,Hiroo Kumagai,Naoki Oshima
出处
期刊:American Journal of Physiology-renal Physiology
[American Physical Society]
日期:2021-11-01
卷期号:321 (6): F757-F770
被引量:22
标识
DOI:10.1152/ajprenal.00191.2021
摘要
We classified kidney macrophages (Mφs) into bone marrow-derived (BM-) macrophages expressing high CD11b and tissue-specific resident (Res-) macrophages expressing low CD11b. In diabetic nephropathy (DN) model mice, TLR9 expression and TNF-α production via TLR9 activation in BM-Mφs and ROS production in Res-Mφs were enhanced. Furthermore, CCR2 antagonist suppressed the kidney infiltration of BM-Mφs and their function and the ROS production by Res-Mφs, with concomitant TLR9 suppression. Our study presents a new therapeutic strategy for DN.
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