Understanding the heterogeneity of natural killer cells at the maternal-fetal interface: implications for pregnancy health and disease

被引:1
|
作者
Zhang, Yuying [1 ,2 ]
Yang, Liangtao [3 ,4 ,5 ]
Yang, Dongyong [1 ,2 ]
Cai, Songchen [3 ,4 ,5 ]
Wang, Yanjun [1 ,2 ]
Wang, Linlin [1 ,2 ,3 ,4 ,5 ]
Li, Yuye [3 ,4 ,5 ]
Li, Longfei [3 ,4 ,5 ]
Yin, Tailang [1 ,2 ]
Diao, Lianghui [2 ,3 ,4 ,5 ]
机构
[1] Wuhan Univ, Renmin Hosp, Reprod Med Ctr, 99 Zhangzhidong Rd, Wuhan 430060, Hubei, Peoples R China
[2] Hubei Clin Res Ctr Assisted Reprod Technol & Embry, 99 Zhangzhidong Rd, Wuhan 430060, Hubei, Peoples R China
[3] Shenzhen Zhongshan Obstet & Gynecol Hosp, Shenzhen Zhongshan Inst Reprod Med & Genet, Shenzhen Key Lab Reprod Immunol Periimplantat, 1001 Fuqiang Rd, Shenzhen 518045, Guangdong, Peoples R China
[4] Shenzhen Zhongshan Urol Hosp, Shenzhen, Peoples R China
[5] Guangdong Engn Technol Res Ctr Reprod Immunol Peri, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
maternal-fetal interface; uterine natural killer cells; single-cell RNA sequencing; categorization; pregnancy complications; immunity; endometrium; decidua; UTERINE NK CELLS; IMPLANTATION; PATHOGENESIS; FAILURE; WOMEN;
D O I
10.1093/molehr/gaae040
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Natural killer (NK) cells are the most abundant leukocytes located at the maternal-fetal interface; they respond to pregnancy-related hormones and play a pivotal role in maintaining the homeostatic micro-environment during pregnancy. However, due to the high heterogeneity of NK cell subsets, their categorization has been controversial. Here, we review previous studies on uterine NK cell subsets, including the classic categorization based on surface markers, functional molecules, and developmental stages, as well as single-cell RNA sequencing-based clustering approaches. In addition, we summarize the potential pathways by which endometrial NK cells differentiate into decidual NK (dNK) cells, as well as the differentiation pathways of various dNK subsets. Finally, we compared the alterations in the NK cell subsets in various pregnancy-associated diseases, emphasizing the possible contribution of specific subsets to the development of the disease.
引用
收藏
页数:14
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