Wilkin Allison M, Harnett Amber, Underschultz Michael, Cragg Cheryl, Meckling Kelly A
Department of Human Health and Nutritional Sciences, University of Guelph, 50 Stone Rd E, Guelph, ON N1G 2W1, Canada.
Department of Human Health and Nutritional Sciences, University of Guelph, 50 Stone Rd E, Guelph, ON N1G 2W1, Canada.
Steroids. 2018 Jul;135:63-68. doi: 10.1016/j.steroids.2018.02.006. Epub 2018 Feb 23.
The protein disulfide isomerase ERp57 (GRp58/PDIA3/1,25D3-MARRS) has been implicated in a multitude of signaling pathways throughout the entire body. Most thoroughly studied for its protein-folding role, ERp57 has also been found to have multiple binding partners, and have significant effects on cellular growth. ERp57 has been studied n the context of several neurodegenerative disorders, metabolic conditions, and can be used as a prognosis marker in certain cancers. One role, as an alternate vitamin D binding receptor, has prompted research in tissues with known vitamin D activity, such as the intestine and bone. Vitamin D has been studied in relation to mammary gland growth and development, but it is not yet known if ERp57 plays an independent role in this tissue. In this study, ERp57 was knocked out in murine mammary gland epithelial cells of 30 4-week old mice. Several markers of mammary gland growth were measured, including number of terminal end buds (TEB), ductal coverage of the fat pad, and ductal extension. It was found the knockout animals had decreased numbers of TEBs (p = 0.019), and decreased ductal extension (p = 0.018) compared to wildtype animals, with no differences in gross body weight. Immunohistochemistry analysis of mammary glands showed ERp57 localized to the apical side of alveolar branches, and on leading edges of TEBs. These results provide further evidence for ERp57 functioning separately to the VDR, and further insights into the roles of ERp57.
蛋白质二硫键异构酶ERp57(GRp58/PDIA3/1,25D3-MARRS)参与了全身多种信号通路。ERp57因其蛋白质折叠作用得到了最深入的研究,还被发现有多个结合伴侣,并对细胞生长有显著影响。在几种神经退行性疾病、代谢状况的背景下对ERp57进行了研究,它还可作为某些癌症的预后标志物。作为一种替代性维生素D结合受体的作用,促使人们在具有已知维生素D活性的组织,如肠道和骨骼中开展研究。已经对维生素D与乳腺生长发育的关系进行了研究,但尚不清楚ERp57在该组织中是否发挥独立作用。在本研究中,敲除了30只4周龄小鼠的乳腺上皮细胞中的ERp57。测量了几种乳腺生长标志物,包括末端终芽(TEB)数量、脂肪垫的导管覆盖率和导管延伸情况。结果发现,与野生型动物相比,敲除动物的TEB数量减少(p = 0.019),导管延伸减少(p = 0.018),总体体重无差异。对乳腺的免疫组织化学分析显示,ERp57定位于肺泡分支的顶端以及TEB的前沿。这些结果为ERp57独立于维生素D受体发挥作用提供了进一步证据,并对ERp57的作用有了更深入的了解。