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首页> 外文期刊>Developmental and Comparative Immunology: Ontogeny, Phylogeny, Aging: The Official Journal of the International Society of Developmental and Comparative Immunology >Differential expression and functional roles of chemokine (C-C motif) ligand 23 and its receptor chemokine (C-C motif) receptor type 1 in the uterine endometrium during early pregnancy in pigs
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Differential expression and functional roles of chemokine (C-C motif) ligand 23 and its receptor chemokine (C-C motif) receptor type 1 in the uterine endometrium during early pregnancy in pigs

机译:冬季妊娠早孕期间,趋化因子(C-C基序)配体23及其受体趋化因子(C-C基序)受体型1型受体1的差异表达及其受体趋化因子受体1

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摘要

Many chemokines expressed by cells of the uterine endometrium of mammals are involved in cell-cell interactions. However, little is known about expression and functional roles of chemokine (C-C motif) ligand 23 (CCL23) in the uterine endometrium. Results of this study demonstrated that CCL23 and its receptor, chemokine (C-C motif) receptor type 1 (CCR1), are up-regulated in porcine endometria during pregnancy. CCL23 and CCR1 mRNAs were strongly expressed in endometrial glandular (GE) and luminal (LE) epithelial cells. Treatment of porcine uterine luminal epithelial (pLE) cells with recombinant CCL23 increased the abundances of PCNA and cyclin D1, and enhanced proliferation and cell cycle progression in pLE cells. CCL23 also stimulated phosphorylation of cell signaling molecules including AKT and MAPKs in pLE cells. Furthermore, ER stress-related molecules were reduced by CCL23. These results suggest that CCL23-CCR1 signaling is important for endometrial development and establishment of pregnancy in pigs. (C) 2017 Elsevier Ltd. All rights reserved.
机译:由哺乳动物子宫子宫内膜细胞表达的许多趋化因子参与细胞 - 细胞相互作用。然而,关于子宫子宫内膜中的趋化因子(C-C基序)配体23(CCL23)的表达和功能作用很少。该研究的结果证明,CCL23及其受体,趋化因子(C-C基序)受体1(CCR1),在妊娠期间在猪子宫内膜中调节。 CCL23和CCR1 mRNA在子宫内膜腺(GE)和腔(LU)上皮细胞中强烈表达。用重组CCL23治疗猪子宫腔上皮(PLE)细胞增加了PCNA和细胞周期蛋白D1的丰度,并增强了PLE细胞中的增殖和细胞周期进展。 CCL23还刺激了在Ple细胞中包括AKT和MAPK的细胞信号传导分子的磷酸化。此外,CCL23还减少了ER应激相关的分子。这些结果表明,CCL23-CCR1信号传导对子宫内膜发育和猪怀孕的建立很重要。 (c)2017 Elsevier Ltd.保留所有权利。

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