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本文引用的文献

1
From initial segment to cauda: a regional characterization of mouse epididymal CD11c mononuclear phagocytes based on immune phenotype and function.从起始段到尾部:基于免疫表型和功能的小鼠附睾 CD11c 单核吞噬细胞的区域性特征。
Am J Physiol Cell Physiol. 2020 Dec 1;319(6):C997-C1010. doi: 10.1152/ajpcell.00392.2020. Epub 2020 Sep 29.
2
Generation, localization and functions of macrophages during the development of testis.在睾丸发育过程中巨噬细胞的生成、定位和功能。
Nat Commun. 2020 Sep 1;11(1):4375. doi: 10.1038/s41467-020-18206-0.
3
Differential tissue-specific damage caused by bacterial epididymo-orchitis in the mouse.细菌性附睾睾丸炎在小鼠中引起的组织特异性差异损伤。
Mol Hum Reprod. 2020 Apr 24;26(4):215-227. doi: 10.1093/molehr/gaaa011.
4
Region-specific transcriptomic and functional signatures of mononuclear phagocytes in the epididymis.附睾中单核吞噬细胞的区域特异性转录组和功能特征。
Mol Hum Reprod. 2020 Jan 1;26(1):14-29. doi: 10.1093/molehr/gaz059.
5
Fate Mapping via Ms4a3-Expression History Traces Monocyte-Derived Cells.通过 Ms4a3 表达史轨迹追踪单核细胞来源细胞进行命运映射。
Cell. 2019 Sep 5;178(6):1509-1525.e19. doi: 10.1016/j.cell.2019.08.009.
6
Two distinct interstitial macrophage populations coexist across tissues in specific subtissular niches.两种不同的组织间巨噬细胞群体存在于特定的组织亚区隔龛位中。
Science. 2019 Mar 15;363(6432). doi: 10.1126/science.aau0964.
7
Self-renewing resident cardiac macrophages limit adverse remodeling following myocardial infarction.心肌梗死后,自我更新的驻留心肌巨噬细胞限制了不良重构。
Nat Immunol. 2019 Jan;20(1):29-39. doi: 10.1038/s41590-018-0272-2. Epub 2018 Dec 11.
8
Lack of the pH-sensing Receptor TDAG8 [GPR65] in Macrophages Plays a Detrimental Role in Murine Models of Inflammatory Bowel Disease.缺乏 pH 感应受体 TDAG8[GPR65]在巨噬细胞中在炎症性肠病的小鼠模型中发挥有害作用。
J Crohns Colitis. 2019 Feb 1;13(2):245-258. doi: 10.1093/ecco-jcc/jjy152.
9
Lipopolysaccharide-induced testicular dysfunction and epididymitis in mice: a critical role of tumor necrosis factor alpha†.脂多糖诱导的小鼠睾丸功能障碍和附睾炎炎:肿瘤坏死因子 α 的关键作用†。
Biol Reprod. 2019 Mar 1;100(3):849-861. doi: 10.1093/biolre/ioy235.
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Tissue-resident macrophages in the intestine are long lived and defined by Tim-4 and CD4 expression.肠道组织驻留巨噬细胞寿命长,其特征是表达 Tim-4 和 CD4。
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成年附睾和睪丸中存在两种自我维持的单核细胞非依赖性巨噬细胞群体。

Two populations of self-maintaining monocyte-independent macrophages exist in adult epididymis and testis.

机构信息

Medical Research Center, The First Affiliated Hospital of Zhengzhou University, 450052 Zhengzhou, China.

Institute of Anatomy and Cell Biology, Unit of Reproductive Biology, Justus-Liebig University Giessen, 35392 Giessen, Germany.

出版信息

Proc Natl Acad Sci U S A. 2021 Jan 5;118(1). doi: 10.1073/pnas.2013686117.

DOI:
10.1073/pnas.2013686117
PMID:33372158
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7817195/
Abstract

Macrophages are the principal immune cells of the epididymis and testis, but their origins, heterogeneity, development, and maintenance are not well understood. Here, we describe distinct populations of epididymal and testicular macrophages that display an organ-specific cellular identity. Combining in vivo fate-mapping, chimeric and parabiotic mouse models with in-depth cellular analyses, we found that CD64MHCII and CD64MHCII macrophage populations of epididymis and testis arise sequentially from yolk sac erythro-myeloid progenitors, embryonic hematopoiesis, and nascent neonatal monocytes. While monocytes were the major developmental source of both epididymal and testicular macrophages, both populations self-maintain in the steady-state independent of bone marrow hematopoietic precursors. However, after radiation-induced macrophage ablation or during infection, bone marrow-derived circulating monocytes are recruited to the epididymis and testis, giving rise to inflammatory macrophages that promote tissue damage. These results define the layered ontogeny, maintenance and inflammatory response of macrophage populations in the male reproductive organs.

摘要

巨噬细胞是附睾和睾丸的主要免疫细胞,但它们的起源、异质性、发育和维持尚不清楚。在这里,我们描述了附睾和睾丸中具有器官特异性细胞特征的不同巨噬细胞群体。通过体内示踪、嵌合和联体小鼠模型与深入的细胞分析相结合,我们发现附睾和睾丸的 CD64MHCII 和 CD64MHCII 巨噬细胞群是从卵黄囊红髓造血前体细胞、胚胎造血和新生新生儿单核细胞中依次出现的。虽然单核细胞是附睾和睾丸中两种巨噬细胞的主要发育来源,但在稳态下,它们都可以独立于骨髓造血前体自我维持。然而,在辐射诱导的巨噬细胞耗竭或感染后,骨髓来源的循环单核细胞被招募到附睾和睾丸中,产生促炎巨噬细胞,导致组织损伤。这些结果定义了男性生殖器官中巨噬细胞群体的分层发生、维持和炎症反应。