Peng Wang , Qunxiong Zeng , Jin-Chuan Liu , Chen Yang , Dali Tong , Yanfeng Li , Yong-Gang Duan
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引用次数: 0
摘要
急性附睾睾丸炎对睾丸造成的长期损害在很大程度上仍未得到阐明,这可能是导致男性不育的一个被忽视的因素。本研究采用流式细胞术分析了脂多糖(LPS)诱导的小鼠附睾睾丸炎在第1天、第7天和第28天睾丸免疫细胞亚群的不同表型。随着接种的进行,睾丸中巨噬细胞、中性粒细胞和髓源性抑制细胞(MDSCs)的数量稳步下降。F4/80-CD11c+树突状细胞(DC)总数保持相对稳定的水平,而传统的1型树突状细胞(cDC1)从第1天到第28天逐渐增加。CD4+和CD8+T细胞的数量在第1天和第7天较低,它们的结果相似,在第28天达到上限水平。与附睾相比,睾丸在接种后 28 天显示出较高水平的 CD3+ T 细胞,但巨噬细胞、cDC2 和中性粒细胞的频率较低。总之,我们的数据表明急性附睾睾丸炎可导致睾丸的长期损伤,其特征是由 CD3+ T 细胞(包括 CD4+ 和 CD8+ T 细胞)介导的免疫反应。
Immunodeviation towards T cell-mediated immune response in the testes of LPS-induced mouse epididymo-orchitis
The testicular consequences of acute epididymo-orchitis remain largely unelucidated in long-term damage, which might be a neglected factor for male infertility. In this study, the differential phenotype of testicular immune cell subpopulations in lipopolysaccharide (LPS)-induced mouse epididymo-orchitis were analyzed by flow cytometry on day 1, day 7, and day 28. The number of macrophages, neutrophils, and myeloid-derived suppressor cells (MDSCs) steadily decreased in the testes with inoculation. Total F4/80-CD11c+ dendritic cells (DCs) maintained a relatively stable level, whereas conventional type 1 dendritic cells (cDC1) increased gradually from day 1 to day 28. There was a lower number of CD4+ and CD8+ T cells at day 1 and day 7, and they had similar results with a ceiling level at day 28. The testes displayed a higher level of CD3+ T cells but a lower frequency of macrophages, cDC2, and neutrophils at 28 days post-inoculation compared with the epididymis. In summary, our data indicates acute epididymo-orchitis could lead to long-term damage in the testes, which is characterized by CD3+ T cell (including CD4+ and CD8+ T cells)-mediated immune responses.
期刊介绍:
Affiliated with the European Society of Reproductive Immunology and with the International Society for Immunology of Reproduction
The aim of the Journal of Reproductive Immunology is to provide the critical forum for the dissemination of results from high quality research in all aspects of experimental, animal and clinical reproductive immunobiology.
This encompasses normal and pathological processes of:
* Male and Female Reproductive Tracts
* Gametogenesis and Embryogenesis
* Implantation and Placental Development
* Gestation and Parturition
* Mammary Gland and Lactation.