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Chemoattraction of bone marrow-derived stem cells towards human endometrial stromal cells is mediated by estradiol regulated CXCL12 and CXCR4 expression

机译:雌二醇调节的CXCL12和CXCR4表达介导骨髓干细胞向人子宫内膜基质细胞的化学引诱

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摘要

Bone marrow derived cells engraft to the uterine endometrium and contribute to endometriosis. The mechanism by which these cells are mobilized and directed to the endometrium has not been previously characterized. We demonstrate that human endometrial stromal cells (hESCs) produce the chemokine CXCL12 and that bone marrow cells (BMCs) express the CXCL12 receptor, CXCR4. Treatment with physiological levels of estradiol (E2) induced both CXCL12 and CXCR4 expression in hESCs and BMCs, respectively. BMCs migrated towards hESCs conditioned media; a CXCR4 antagonist blocked migration indicating that CXCL12 acting through its receptor, CXCR4, is necessary for chemoattraction of BM cells to human endometrial cells. E2 increased both CXCL12 expression in endometrial cells and CXCR4 expression in BM cells, further enhancing chemoattraction. E2 induced CXCL12/CXCR4 expression in endometrium and BM, respectively, drives migration of stem cells to the endometrium. The E2-CXCL12/CXCR4 signaling pathway may be useful in determining treatments for endometrial disorders, and may be antagonized to block stem cell migration to endometriosis.
机译:骨髓来源的细胞移植到子宫内膜并促进子宫内膜异位。这些细胞动员并定向到子宫内膜的机制尚未被表征。我们证明了人类子宫内膜基质细胞(hESCs)产生趋化因子CXCL12,而骨髓细胞(BMCs)表达CXCL12受体CXCR4。生理水平的雌二醇(E2)处理分别诱导hESCs和BMC中CXCL12和CXCR4表达。 BMC向hESCs条件培养基迁移; CXCR4拮抗剂阻止了迁移,表明通过其受体CXCR4起作用的CXCL12对于BM细胞向人子宫内膜细胞的化学引诱是必需的。 E2增加子宫内膜细胞中CXCL12的表达和BM细胞中CXCR4的表达,从而进一步增强趋化性。 E2诱导子宫内膜和BM中CXCL12 / CXCR4的表达分别驱动干细胞向子宫内膜迁移。 E2-CXCL12 / CXCR4信号传导途径可用于确定子宫内膜疾病的治疗方法,并可拮抗阻止干细胞向子宫内膜异位症的迁移。

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