Glucocorticoids maintain the extracellular matrix of differentiated mammary tissue during explant and whole organ culture.

T M Casey, A Boecker, J F Chiu, K Plaut
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Abstract

Mouse mammary whole organ culture (WOC) and explant culture of lactating tissue were used to investigate the mechanism by which glucocorticoids maintain secretory epithelium following lobuloalveolar development. The relative number of mammary epithelial cells expressing glucocorticoid receptors did not change with the loss of secretory epithelium during involution as demonstrated with competitive binding assays and immunohistochemistry for the glucocorticoid receptor. Furthermore, glucocorticoids did not inhibit AP-1 binding activity. However, Northern analysis demonstrated that genes associated with the breakdown of the extracellular matrix were not expressed in tissues cultured with glucocorticoids, in contrast to their upregulation during involution of mammary tissue cultured with insulin alone. Tissue inhibitor of metalloproteinase-1 (TIMP-1) mRNA expression was lowest in tissue cultured in the presence of glucocorticoids and increased 2.3-, 3.4-, and 9-fold when tissues were involuted in the presence of insulin (Ins) alone, Ins and hydrocortisone (Hyd) with 0. 005 mg/ml, or 0.01 mg/ml collagenase IV, respectively. These data indicate that glucocorticoids maintain mammary differentiation in part by inhibiting the turnover of basement membrane.

糖皮质激素在移植和整个器官培养过程中维持分化乳腺组织的细胞外基质。
采用小鼠乳腺全器官培养(WOC)和泌乳组织外植体培养,探讨糖皮质激素维持小叶肺泡发育后分泌上皮的机制。表达糖皮质激素受体的乳腺上皮细胞的相对数量并没有随着分泌上皮的丧失而改变,正如糖皮质激素受体的竞争性结合试验和免疫组织化学所证明的那样。此外,糖皮质激素不抑制AP-1的结合活性。然而,Northern的分析表明,与细胞外基质分解相关的基因在糖皮质激素培养的组织中不表达,而在单独使用胰岛素培养的乳腺组织中,它们的表达上调。组织金属蛋白酶抑制剂-1 (TIMP-1) mRNA的表达在糖皮质激素存在的情况下最低,而在胰岛素(Ins)单独存在、Ins和氢化可的松(Hyd)存在的情况下,TIMP-1 mRNA的表达分别增加2.3倍、3.4倍和9倍。分别为0.05 mg/ml或0.01 mg/ml胶原酶IV。这些数据表明糖皮质激素在一定程度上通过抑制基底膜的更新来维持乳腺分化。
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