Human adipose ECM alleviates radiation-induced skin fibrosis via endothelial cell-mediated M2 macrophage polarization.
Human adipose ECM alleviates radiation-induced skin fibrosis via endothelial cell-mediated M2 macrophage polarization.
复制标题
人脂肪ECM通过内皮细胞介导的M2巨噬细胞极化抑制辐射诱导的皮肤纤维化
DOI:
10.1016/j.isci.2023.107660
复制
发表时间:
2023-09-15
期刊:
影响因子:
5.8
通讯作者:
Ejaz, Asim
中科院分区:
文献类型:
--
作者:
Chinnapaka, Somaiah;Yang, Katherine S.;Surucu, Yusuf;Bengur, Fuat B.;Arellano, Jose A.;Tirmizi, Zayaan;Malekzadeh, Hamid;Epperly, Michael W.;Hou, Wen;Greenberger, Joel S.;Rubin, J. Peter;Ejaz, Asim
Radiation therapy can lead to late radiation-induced skin fibrosis (RISF), causing movement restriction, pain, and organ dysfunction. This study evaluated adipose-derived extracellular matrix (Ad-ECM) as a mitigator of RISF. Female C57BL/6J mice that were irradiated developed fibrosis, which was mitigated by a single local Ad-ECM injection, improving limb movement and reducing epithelium thickness and collagen deposition. Ad-ECM treatment resulted in decreased expression of pro-inflammatory and fibrotic genes, and upregulation of anti-inflammatory cytokines, promoting M2 macrophage polarization. Co-culture of irradiated human fibroblasts with Ad-ECM down-modulated fibrotic gene expression and enhanced bone marrow cell migration. Ad-ECM treatment also increased interleukin (IL)-4, IL-5, and IL-15 expression in endothelial cells, stimulating M2 macrophage polarization and alleviating RISF. Prophylactic use of Ad-ECM showed effectiveness in mitigation. This study suggests Ad-ECM’s potential in treating chronic-stage fibrosis. Ad-ECM can effectively mitigate RISF M2 macrophage polarization plays a crucial role in mitigation Ad-ECM offers prophylactic mitigation potential to RISF Cell biology; Dermatology; Fibrosis; Immunology; Stem cells research
登录
查看更多内容
影响因子:
3.6
作者:
Garza RM;Paik KJ;Chung MT;Duscher D;Gurtner GC;Longaker MT;Wan DC
通讯作者:
Wan DC
影响因子:
7.8
作者:
Huleihel L;Dziki JL;Bartolacci JG;Rausch T;Scarritt ME;Cramer MC;Vorobyov T;LoPresti ST;Swineheart IT;White LJ;Brown BN;Badylak SF
通讯作者:
Badylak SF
影响因子:
1
作者:
Akita, S.;Yoshimoto, H.;Yamashita, S.
通讯作者:
Yamashita, S.
影响因子:
3.7
作者:
Gallet P;Phulpin B;Merlin JL;Leroux A;Bravetti P;Mecellem H;Tran N;Dolivet G
通讯作者:
Dolivet G
影响因子:
14
作者:
Brown, Bryan N.;Valentin, Jolene E.;Stewart-Akers, Ann M.;McCabe, George P.;Badylak, Stephen F.
通讯作者:
Badylak, Stephen F.