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Mammary gland serotonin regulates parathyroid hormone-related protein and other bone-related signals

机译:乳腺5-羟色胺调节甲状旁腺激素相关蛋白和其他骨相关信号

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摘要

Breast cells drive bone demineralization during lactation and metastatic cancers. A shared mechanism among these physiological and pathological states is endocrine secretion of parathyroid hormone-related protein (PTHrP), which acts through osteoblasts to stimulate osteoclastic bone demineralization. The regulation of PTHrP has not been accounted for fully by any conventional mammotropic stimuli or tumor growth factors. Serotonin (5-HT) synthesis within breast epithelial cells is induced during lactation and in advancing breast cancer. Here we report that serotonin deficiency (knockout of tryptophan hydroxylase-1) results in a reduction of mammary PTHrP expression during lactation, which is rescued by restoring 5-HT synthesis. 5-HT induced PTHrP expression in lactogen-primed mammary epithelial cells from either mouse or cow. In human breast cancer cells 5-HT induced both PTHrP and the metastasis-associated transcription factor Runx2/Cbfa1. Based on receptor expression and pharmacological evidence, the 5-HT2 receptor type was implicated as being critical for induction of PTHrP and Runx2. These results connect 5-HT synthesis to the induction of bone-regulating factors in the normal mammary gland and in breast cancer cells. ? 2012 the American Physiological Society.
机译:乳细胞在哺乳期和转移性癌症中驱动骨骼脱矿质。这些生理和病理状态之间共有的机制是甲状旁腺激素相关蛋白(PTHrP)的内分泌分泌,该蛋白通过成骨细胞刺激破骨细胞脱矿质。任何常规的促乳动刺激或肿瘤生长因子都不能完全解释PTHrP的调节。哺乳期间和晚期乳腺癌中会诱导上皮细胞内的5-羟色胺(5-HT)合成。在这里,我们报告血清素缺乏症(色氨酸羟化酶-1的敲除)导致泌乳期间乳腺PTHrP表达的减少,这是通过恢复5-HT合成来解决的。 5-HT诱导小鼠或母牛的乳原引发的乳腺上皮细胞中的PTHrP表达。在人类乳腺癌细胞中,5-HT诱导了PTHrP和与转移相关的转录因子Runx2 / Cbfa1。根据受体表达和药理证据,暗示5-HT2受体类型对于诱导PTHrP和Runx2至关重要。这些结果将5-HT合成与正常乳腺和乳腺癌细胞中骨调节因子的诱导联系起来。 ? 2012年美国生理学会。

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