School of Health & Life Science, University of the West of Scotland, Paisley, UK.
Obstetrics & Gynaecology, College of Medicine, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Immunol Invest. 2020 Apr;49(3):264-286. doi: 10.1080/08820139.2019.1655573. Epub 2019 Aug 20.
Homeostatic leukocyte trafficking into and within the female reproductive tract (FRT) contributes to fertility and reproductive health. It is unclear how this process is regulated in the anatomically distinct reproductive tissues, or whether the genes involved are affected by cyclical changes in reproductive hormones. In tissues such as skin and intestine, mouse studies have defined evolutionarily conserved molecular mechanisms for tissue-specific homing, interstitial positioning, and leukocyte egress. Chemokine family members are invariably involved, with the chemokine expression profile of a tissue regulating leukocyte content. Reproductive tissues (ovary, vagina, cervix, uterine horn) of 8 week old virgin female C57BL/6 mice () were collected, and expression of mRNA for leukocyte markers and chemokines conducted by qPCR. Lymphocytic and myeloid cell populations within the uterus, cervix, bone marrow and PALN from virgin C57BL/6 mice were determined by flow cytometric analysis. Variation in leukocyte content between reproductive tissues is evident, with the uterus and cervix containing complex mixtures of lymphocytes and myeloid cells. Twenty-six chemokine genes are expressed in the FRT, many by several component tissues, some preferentially by one. Most striking are and , which are restricted to the uterus. and genes encoding CXCR2 ligands are primarily transcribed in cervix and vagina. Ovary shows the lowest expression of most chemokine genes, with the notable exception of and . We also identify eight chemokines in the vagina whose expression fluctuates substantially across the oestrous cycle. These data reveal complex chemokine networks within the FRT, and provide a framework for future studies of homeostatic leukocyte trafficking into and within these tissues.: BM: bone marrow; DC: dendritic cell; DN: double negative; FRT: female reproductive tract; FSC: forward scatter; NK: natural killer; PALN: para-aortic lymph node; SSC: side scatter; Tregs: regulatory T cells.
稳态白细胞向女性生殖道(FRT)内和在其内的迁移有助于生育和生殖健康。目前尚不清楚这一过程在解剖学上不同的生殖组织中是如何被调控的,也不清楚参与其中的基因是否受到生殖激素周期性变化的影响。在皮肤和肠道等组织中,小鼠研究已经定义了用于组织特异性归巢、间质定位和白细胞出胞的进化保守的分子机制。趋化因子家族成员始终参与其中,组织的趋化因子表达谱调节白细胞含量。收集 8 周龄处女 C57BL/6 小鼠的卵巢、阴道、子宫颈和子宫角等生殖组织,并通过 qPCR 检测白细胞标志物和趋化因子的 mRNA 表达。通过流式细胞术分析,确定处女 C57BL/6 小鼠子宫、子宫颈、骨髓和 PALN 中的淋巴细胞和髓样细胞群体。生殖组织之间的白细胞含量存在明显差异,子宫和子宫颈含有淋巴细胞和髓样细胞的复杂混合物。FRT 中有 26 个趋化因子基因表达,其中许多由几个组成组织表达,有些则优先由一个组织表达。最引人注目的是 和 ,它们仅局限于子宫。 和编码 CXCR2 配体的基因主要在宫颈和阴道中转录。卵巢表达大多数趋化因子基因的水平最低,但 和 除外。我们还在阴道中鉴定出 8 种表达在整个发情周期中波动很大的趋化因子。这些数据揭示了 FRT 内复杂的趋化因子网络,并为未来研究这些组织中稳态白细胞的迁移提供了框架。:BM:骨髓;DC:树突状细胞;DN:双阴性;FRT:女性生殖道;FSC:前向散射;NK:自然杀伤;PALN:腹主动脉旁淋巴结;SSC:侧向散射;Tregs:调节性 T 细胞。