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首页> 外文期刊>Hormone and Metabolic Research >Thyroid-Stimulating Hormone-Stimulated Human Adipocytes Express Thymic Stromal Lymphopoietin
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Thyroid-Stimulating Hormone-Stimulated Human Adipocytes Express Thymic Stromal Lymphopoietin

机译:甲状腺刺激激素刺激的人脂肪细胞表达胸腺基质淋巴二胞胎

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When recombinant human (rh) thyroid-stimulating hormone (TSH) is administered to thyroid cancer survivors, an acute extra-thyroidal effect raises pro-inflammatory cytokines and activates platelets. Thymic stromal lymphopoietin (TSLP) is a cytokine recently implicated in platelet activation. Our aim was to measure platelet microparticle levels after rhTSH stimulation in vivo, and to investigate TSLP expression in TSH-stimulated human adipocytes in culture. Blood samples for total and platelet microparticle analysis were obtained from thyroid cancer survivors before (day 1) and after rhTSH administration (day 5). Adipocytes, differentiated from stromal preadipocytes isolated from adipose tissue from surgical patients, were stimulated with TSH. TSLP mRNA expression, protein expression, and protein release into the adipocyte medium were measured. The level of platelet microparticles in thyroid cancer patients rose 5-fold after rhTSH stimulation. TSH upregulated TSLP mRNA expression in adipocytes in culture through a pathway that was inhibited by 66% by H89, a protein kinase A inhibitor. TSLP protein expression rose in response to TSH, and TSH-stimulated TSLP release into the medium was completely blocked by dexamethasone. In conclusion, TSLP is a novel TSH-responsive adipokine. Future studies will be needed to address the potential role of adipocyte-derived TSLP and whether it is linked to TSH-dependent platelet activation.
机译:当对甲状腺癌幸存者给予重组人(RH)甲状腺刺激激素(TSH)时,急性超甲状腺效果提高了促炎细胞因子并激活血小板。胸腺基质淋巴细胞素(TSLP)是一种最近血小板活化的细胞因子。我们的目标是测量体内刺激刺激后的血小板微粒水平,并在培养的TSH刺激的人脂肪细胞中调查TSLP表达。从甲状腺癌幸存者(第1天)和Rhtsh施用之后(第5天)获得血小板微粒分析的血液样品。用来自外科患者分离的来自脂肪组织中分离的基质前脂肪细胞的脂肪细胞被TSH刺激。测量TSLP mRNA表达,蛋白表达和蛋白质释放到脂肪细胞培养基中。甲状腺癌患者的血小板微粒水平上升5倍后刺激刺激。 TSH通过H89抑制66%的途径,培养涉及培养的脂肪细胞中的TSH上调的TSLP mRNA表达,蛋白激酶抑制剂。 TSLP蛋白表达响应于TSH,TSH刺激的TSLP释放到培养基中被地塞米松完全阻断。总之,TSLP是一种新型TSH响应性adipokine。将来需要进行未来的研究来解决脂肪细胞衍生TSLP的潜在作用以及是否与TSH依赖性血小板激活相关联。

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