间质细胞
伤口愈合
医学
前列腺
癌症研究
吉非替尼
细胞因子
趋化因子
旁分泌信号
病理
表皮生长因子受体
炎症
内科学
免疫学
受体
癌症
作者
Fei Shi,Zheng Deng,Zheng Zhou,Bo Jiang,Chenyi Jiang,Ruizhe Zhao,Feng Sun,Di Cui,Meng‐Hao Sun,Qian Sun,Xing‐Jie Wang,Qi Wu,Shujie Xia,Bang‐Min Han
出处
期刊:The Prostate
[Wiley]
日期:2019-05-24
卷期号:79 (11): 1238-1255
被引量:16
摘要
Background This study investigated shallow heat injury to prostate stromal fibroblasts and epithelial cells and their interaction to regulate the wound healing and the underlying molecular events. Methods Prostate stromal fibroblasts and epithelial cells were cultured individually or cocultured and subjected to shallow heat injury for assessments of cell proliferation, migration, apoptosis, cell cycle distribution, and gene expression. The supernatant of heat‐injured WPMY‐1 cells was collected for exosome extraction and assessments. Furthermore, beagle dogs received thulium laser resection of the prostate (TmLRP) and randomly divided into Gefitinib, GW4869, and control treatment for the histological analysis, tissue re‐epithelialization, and epidermal growth factor receptor (EGFR) expression on the prostatic wound surface. Immunofluorescence was to evaluate p63‐positive basal progenitor cell trans‐differentiation and macrophage polarization and ELISA was to detect cytokine levels in beagles' urine. Results Shallow heat injury caused these cells to enter a stressed state and enhanced their crosstalk. The prostate stromal fibroblasts produced and secreted more exosomal‐EGFR and other cytokines and chemokines after shallow heat injury, resulting in increased proliferation and migration of prostate epithelial cells during wound healing. The wound healing of the canine prostatic urethra following the TmLRP procedure was slower in the Gefitinib and GW4869 treatment group than in the control group of animals. Immunofluorescence and ELISA showed that reduced EGFR expression interrupted macrophage polarization but increased the inflammatory response. Conclusions Shallow heat injury was able to promote the interaction of prostate stromal cells with prostate epithelial cells to enhance wound healing. Stromal‐derived exosomal‐EGFR plays a crucial role in the balance of the macrophage polarization and prostatic wound healing.
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