首页> 外文期刊>PLoS One >Inhibitory Activity of YKL-40 in Mammary Epithelial Cell Differentiation and Polarization Induced by Lactogenic Hormones: A Role in Mammary Tissue Involution
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Inhibitory Activity of YKL-40 in Mammary Epithelial Cell Differentiation and Polarization Induced by Lactogenic Hormones: A Role in Mammary Tissue Involution

机译:YKL-40在乳腺激素诱导的乳腺上皮细胞分化和极化中的抑制活性:在乳腺组织退化中的作用。

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We previously reported that a secreted glycoprotein YKL-40 acts as an angiogenic factor to promote breast cancer angiogenesis. However, its functional role in normal mammary gland development is poorly understood. Here we investigated its biophysiological activity in mammary epithelial development and mammary tissue morphogenesis. YKL-40 was expressed exclusively by ductal epithelial cells of parous and non-parous mammary tissue, but was dramatically up-regulated at the beginning of involution. To mimic ductal development and explore activity of elevated YKL-40 during mammary tissue regression in vivo, we grew a mammary epithelial cell line 76N MECs in a 3-D Matrigel system in the presence of lactogenic hormones including prolactin, hydrocortisone, and insulin. Treatment of 76N MECs with recombinant YKL-40 significantly inhibited acinar formation, luminal polarization, and secretion. YKL-40 also suppressed expression of E-cadherin but increased MMP-9 and cell motility, the crucial mechanisms that mediate mammary tissue remodeling during involution. In addition, engineering of 76N MECs with YKL-40 gene to express ectopic YKL-40 recapitulated the same activities as recombinant YKL-40 in the inhibition of cell differentiation. These results suggest that YKL-40-mediated inhibition of cell differentiation and polarization in the presence of lactogenic hormones may represent its important function during mammary tissue involution. Identification of this biophysiological property will enhance our understanding of its pathologic role in the later stage of breast cancer that is developed from poorly differentiated and highly invasive cells.
机译:我们以前曾报道过,分泌的糖蛋白YKL-40可以作为血管生成因子来促进乳腺癌的血管生成。然而,人们对其在正常乳腺发育中的功能作用了解甚少。在这里,我们调查了其在乳腺上皮发育和乳腺组织形态发生中的生物生理活性。 YKL-40仅由乳腺组织和非乳腺组织的导管上皮细胞表达,但在内卷开始时显着上调。为了模拟导管发育并探索体内乳腺组织消退期间升高的YKL-40的活性,我们在存在泌乳激素(包括催乳素,氢化可的松和胰岛素)的情况下,在3-D Matrigel系统中培养了乳腺上皮细胞系76N MEC。用重组YKL-40处理76N MEC可显着抑制腺泡形成,管腔极化和分泌。 YKL-40还抑制E-钙黏着蛋白的表达,但增加MMP-9和细胞运动性,这是在进化过程中介导乳腺组织重塑的关键机制。另外,用YKL-40基因表达异位YKL-40的76N MECs在抑制细胞分化方面概括了与重组YKL-40相同的活性。这些结果表明,在生乳激素的存在下,YKL-40介导的细胞分化和极化抑制可能代表其在乳腺组织退化过程中的重要功能。鉴定这种生物生理特性将增强我们对其在晚期乳腺癌中的病理学作用的了解,该晚期乳腺癌是由分化程度低和侵入性强的细胞发展而成的。

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