Gong Han, Chen Yilu, Xu Jingjie, Xie Xingxing, Yu Dainan, Yang Bei, Kuang Haibin
Department of Physiology and Jiangxi Provincial Key Laboratory of Reproductive Physiology and Pathology, Basic Medical College, Nanchang University, Nanchang, Jiangxi, 330006, People's Republic of China.
Department of Clinic medicine, School of Queen Mary, Nanchang University, Nanchang, Jiangxi, 330006, People's Republic of China.
Reprod Biol Endocrinol. 2017 Sep 6;15(1):73. doi: 10.1186/s12958-017-0290-1.
Uterine natural killer (uNK) cells are short-lived, terminally differentiated and the most abundant lymphocytes in the uterus which play a crucial role in the spiral arteriole modification and establishment of successful pregnancy. Dysregulation of uNK cells has been linked to gestational implications such as recurrent pregnancy loss, preeclampsia and fetal growth retardation. There is evidence showing that progesterone and estrogen can regulate the recruitment, proliferation, differentiation and function of uNK cells via direct action on intracellular nuclear receptors or through intermediary cells in the uterus during early pregnancy. As the deepening of related research in this field, the role of conceptus in such regulation has received extensive attention, it utilizes endocrine signaling (hCG), juxtacrine signaling (HLA-C, HLA-E, HLA-G) and paracrine signaling (cytokines) to facilitate the activities of uNK cells. In addition, under the influence of ovarian hormones, conceptus can increase expression of PIBF and HLA-G molecules to reduce cytotoxicity of uNK cells and promote angiogenesis. In this review, we aim to concentrate on the novel findings of ovarian hormones in the regulation of uNK cells, emphasize the regulatory role of conceptus on uNK cells and highlight the proposed issues for future research in the field.
子宫自然杀伤(uNK)细胞寿命短暂,终末分化,是子宫中数量最多的淋巴细胞,在螺旋小动脉重塑和成功妊娠的建立中起关键作用。uNK细胞功能失调与复发性流产、先兆子痫和胎儿生长受限等妊娠相关问题有关。有证据表明,在妊娠早期,孕酮和雌激素可通过直接作用于细胞内核受体或通过子宫中的中间细胞来调节uNK细胞的募集、增殖、分化和功能。随着该领域相关研究的深入,胚胎在这种调节中的作用受到广泛关注,它利用内分泌信号(hCG)、旁分泌信号(HLA-C、HLA-E、HLA-G)和自分泌信号(细胞因子)来促进uNK细胞的活性。此外,在卵巢激素的影响下,胚胎可增加PIBF和HLA-G分子的表达,以降低uNK细胞的细胞毒性并促进血管生成。在本综述中,我们旨在聚焦卵巢激素在调节uNK细胞方面的新发现,强调胚胎对uNK细胞的调节作用,并突出该领域未来研究中存在的问题。