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Emerging Themes in Uterine Natural Killer Cell Heterogeneity and Function
被引:13
作者:
Hatta, Kota
[2
,3
]
MacLeod, R. John
[1
]
Gerber, Scott A.
[4
]
Croy, B. Anne
[1
]
机构:
[1] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON K7L 3N6, Canada
[2] Toronto Gen Hosp, Div Cardiovasc Surg, Toronto, ON, Canada
[3] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A1, Canada
[4] Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Rochester, NY 14642 USA
基金:
加拿大健康研究院;
加拿大自然科学与工程研究理事会;
关键词:
Angiogenesis;
blood pressure regulation;
decidua;
gestational programming;
mouse;
pregnancy;
ultrasound;
Wnt signaling;
NK CELLS;
EARLY-PREGNANCY;
MOUSE UTERUS;
REPRODUCTIVE FAILURE;
CD56(BRIGHT) CELLS;
DEFICIENT MICE;
METRIAL GLAND;
EXPRESSION;
ANGIOGENESIS;
DIFFERENTIATION;
D O I:
10.1111/j.1600-0897.2012.01160.x
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Problem Understanding of uterine natural killer (uNK) cell functions during normal pregnancy remains incomplete. Method of study Cloud tag analysis of literature was used to document themes addressed experimentally for uNK cells. Immunohistochemistry, including whole-mount staining of early implantation sites, separation of uNK cells into molecularly distinct subsets, and physiologic measurements in normal and mutant mice, are further advancing understanding of uNK cell biology. Results Literature analyses revealed three key, current uNK cell research themes: angiogenesis, spiral arterial remodeling/pre-eclampsia/hypertension and infertility. UNK cells are being defined as cells potentially regulated by Wnt signaling that are heterogeneous in progenitor source and function and make unique contributions to implantation site development prior to spiral arterial remodeling. Conclusion Future studies are poised to define uNK cell progenitor cells, identify the signaling pathways supporting established uNK cell functions and move current understanding of mouse uNK cells to clinical research questions.
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页码:282 / 289
页数:8
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