Distinct Roles for S100a8 in Early Embryo Development and in the Maternal Deciduum

被引:21
作者
Baker, J. R. [1 ]
Jeffery, R. [2 ]
May, R. D. [1 ]
Mathies, M. [1 ]
Spencer-Dene, B.
Poulsom, R. [2 ]
Hogg, N. [1 ]
机构
[1] Canc Res UK London Res Inst, Leukocyte Adhes Lab, London, England
[2] Canc Res UK London Res Inst, Histopathol Lab, London, England
关键词
S100; proteins; embryo development; vascular tissue; CALCIUM-BINDING PROTEINS; MOLECULAR-PATTERN MOLECULES; NATURAL-KILLER-CELLS; CHEMOTACTIC PROTEIN; MOUSE EMBRYO; IN-VITRO; CP-10; DIFFERENTIATION; NEUTROPHILS; MRP14;
D O I
10.1002/dvdy.22709
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
S100a8 is a cytosolic protein expressed in myeloid cells where it forms a stable heterodimer with another S100 protein family member, S100a9. The S100a9(-/-) mouse is viable and phenotypically normal, whereas the S100a8(-/-) condition is embryonic lethal. We present evidence that S100a8, without S100a9, has a previously unrecognized role in embryo development between fertilization and the 8-cell stage at embryonic day (E) 2.5. S100a8 also has a second role in the maternal deciduum, where expression is associated with the vasculature from the E8.5 stage to the formation of mature placenta. Uterine natural killer cells that have a role in vascular remodelling colocalise with the S100a8 vascular expression in the metrial triangle. In inflammatory responses in peripheral tissues, S100a8 is a potent chemoattractant and also an anti-oxidant. Both roles may be important in the developing placenta. Thus we highlight two new S100a9-independent roles for S100a8 in early embryo development. Developmental Dynamics 240:2194-2203, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:2194 / 2203
页数:10
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