Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions.
Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions.
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DOI:
10.1038/s41467-023-37199-0
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发表时间:
2023-03-15
影响因子:
16.6
通讯作者:
DeFalco, Tony
中科院分区:
文献类型:
--
作者:
Gu, Xiaowei;Heinrich, Anna;Li, Shu-Yun;DeFalco, Tony
A growing body of evidence demonstrates that fetal-derived tissue-resident macrophages have developmental functions. It has been proposed that macrophages promote testicular functions, but which macrophage populations are involved is unclear. Previous studies showed that macrophages play critical roles in fetal testis morphogenesis and described two adult testicular macrophage populations, interstitial and peritubular. There has been debate regarding the hematopoietic origins of testicular macrophages and whether distinct macrophage populations promote specific testicular functions. Here our hematopoietic lineage-tracing studies in mice show that yolk-sac-derived macrophages comprise the earliest testicular macrophages, while fetal hematopoietic stem cells (HSCs) generate monocytes that colonize the gonad during a narrow time window in a Sertoli-cell-dependent manner and differentiate into adult testicular macrophages. Finally, we show that yolk-sac-derived versus HSC-derived macrophages have distinct functions during testis morphogenesis, while interstitial macrophages specifically promote adult Leydig cell steroidogenesis. Our findings provide insight into testicular macrophage origins and their tissue-specific roles. How testis resident macrophages develop and influence tissue function is not fully understood. Here the authors use mouse lineage tracing methods to document the haematopoietic source, development and recruitment of early testicular macrophages, support of foetal testis differentiation, and interaction with, and promotion of steroidogenesis in, Leydig cells.
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影响因子:
16.2
作者:
Dhillon, H;Zigman, JM;Lowelll, BB
通讯作者:
Lowelll, BB
DOI:
10.1007/978-1-60761-869-0_29
发表时间:
2011-01-01
期刊:
SUPPRESSION AND REGULATION OF IMMUNE RESPONSES: METHODS AND PROTOCOLS
影响因子:
--
作者:
Fijak, Monika;Bhushan, Sudhanshu;Meinhardt, Andreas
通讯作者:
Meinhardt, Andreas
影响因子:
8.8
作者:
DeFalco T;Potter SJ;Williams AV;Waller B;Kan MJ;Capel B
通讯作者:
Capel B
影响因子:
4.4
作者:
Grabert, Kathleen;Sehgal, Anuj;Hume, David A.
通讯作者:
Hume, David A.
DOI:
10.1038/mt.2014.112
发表时间:
2014-09
期刊:
Molecular therapy : the journal of the American Society of Gene Therapy
影响因子:
--
作者:
Gow DJ;Sauter KA;Pridans C;Moffat L;Sehgal A;Stutchfield BM;Raza S;Beard PM;Tsai YT;Bainbridge G;Boner PL;Fici G;Garcia-Tapia D;Martin RA;Oliphant T;Shelly JA;Tiwari R;Wilson TL;Smith LB;Mabbott NA;Hume DA
通讯作者:
Hume DA