Developmental origin and maintenance of distinct testicular macrophage populations

被引:116
作者
Mossadegh-Keller, Noushin [1 ]
Gentek, Rebecca [1 ]
Gimenez, Gregory [1 ,2 ]
Bigot, Sylvain [1 ]
Mailfert, Sebastien [1 ]
Sieweke, Michael H. [1 ,2 ]
机构
[1] Aix Marseille Univ, Ctr Immunol Marseille Luminy, CNRS, INSERM, Marseille, France
[2] Max Delbruck Ctr Mol Med, Helmholtzgemeinschaft, Berlin, Germany
基金
欧洲研究理事会;
关键词
SAC-DERIVED MACROPHAGES; TISSUE-RESIDENT MACROPHAGES; CIRCULATING MONOCYTES; SELF-RENEWAL; CARDIAC MACROPHAGES; ADULT LIFE; STEM-CELLS; REVEALS; TESTIS; HOMEOSTASIS;
D O I
10.1084/jem.20170829
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Testicular macrophages (tM phi) are the principal immune cells of the mammalian testis. Beyond classical immune functions, they have been shown to be important for organogenesis, spermatogenesis, and male hormone production. In the adult testis, two different macrophage populations have been identified based on their distinct tissue localization and morphology, but their developmental origin and mode of homeostatic maintenance are unknown. In this study, we use genetic lineage-tracing models and adoptive transfer protocols to address this question. We show that embryonic progenitors give rise to the interstitial macrophage population, whereas peritubular macrophages are exclusively seeded postnatally in the prepuberty period from bone marrow (BM)-derived progenitors. As the proliferative capacity of interstitial macrophages declines, BM progenitors also contribute to this population. Once established, both the peritubular and interstitial macrophage populations exhibit a long life span and a low turnover in the steady state. Our observations identify distinct developmental pathways for two different tM phi populations that have important implications for the further dissection of their distinct roles in organ homeostasis and testicular function.
引用
收藏
页码:2829 / 2841
页数:13
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