A comprehensive evaluation of spontaneous pelvic organ prolapse in rhesus macaques as an ideal model for the study of human pelvic organ prolapse

天狼星红 弹性蛋白 范吉森色斑 灵长类动物 恒河猴 染色 阴道 细胞外基质 医学 病理 免疫组织化学 非人灵长类 生物 解剖 H&E染色 免疫学 细胞生物学 进化生物学 神经科学
作者
Yaqian Li,Jian Liu,Ye Zhang,Meng Mao,Hong Wang,Yidi Ma,Zhigang Chen,Youyue Zhang,Chengmin Liao,Xiaoqing Chang,Qianqian Gao,Jianbin Guo,Yang Ye,Fangfang Ai,Xudong Liu,Xiaoyue Zhao,Weijie Tian,Hua Yang,Weizhi Ji,Tao Tan
出处
期刊:中国科学通报:英文版 卷期号:68 (20): 2434-2447 被引量:16
标识
DOI:10.1016/j.scib.2023.09.003
摘要

Pelvic organ prolapse (POP) seriously affects a woman's quality of life, and the treatment complications are severe. Although new surgical treatments are being developed, the host tissue responses and safety need to be evaluated in preclinical trials. However, there is a lack of suitable animal models, as most quadrupeds exhibit different structural and pathological changes. In this study, 72 elderly rhesus macaques (Macaca mulatta) were physically examined, and the incidence of spontaneous POP was similar to that in humans. The vaginal wall from five control monkeys and four monkeys with POP were selected for further analysis. Verhoeff-van Gieson staining showed that elastin content decreased significantly in monkeys with POP compared with control samples. Immunohistological staining revealed that the smooth muscle bundles in monkey POP appeared disorganized, and the number of large muscle bundles decreased significantly. The collagen I/III ratio in monkey POP also significantly decreased, as revealed by Sirius Red staining. These histological and biochemical changes in monkeys with POP were similar to those in humans with POP. Moreover, we generated a single-cell transcriptomic atlas of the prolapsed monkey vagina. Cross-species analysis between humans and monkeys revealed a comparable cellular composition. Notably, a differential gene expression analysis determined that dysregulation of the extracellular matrix and an immune disorder were the conserved molecular mechanisms. The interplay between fibroblasts and macrophages contributed to human and monkey POP. Overall, this study represents a comprehensive evaluation of spontaneous POP in rhesus macaques and demonstrates that monkeys are a suitable animal model for POP research.
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