Ewan Kenneth B, Shyamala Gopalan, Ravani Shraddha A, Tang Yang, Akhurst Rosemary, Wakefield Lalage, Barcellos-Hoff Mary Helen
Life Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, California 94720, USA.
Am J Pathol. 2002 Jun;160(6):2081-93. doi: 10.1016/s0002-9440(10)61158-3.
Transforming growth factor-beta1 (TGF-beta 1) is a pluripotent cytokine that can inhibit epithelial proliferation and induce apoptosis, but is also widely implicated in breast cancer progression. Understanding its biological action in mammary development is critical for understanding its role in cancer. TGF-beta 1 is produced as a latent complex that requires extracellular activation before receptor binding. To better understand the spatial and temporal regulation of its action during mammary gland development, we examined the pattern of activation in situ using antibodies selected to distinguish between latent and active TGF-beta. Activation was highly restricted. TGF-beta 1 activation was localized primarily to the epithelium, and within the epithelium it was restricted to luminal epithelial cells but absent from either cap or myoepithelial cells. Within the luminal epithelium, we noted a further restriction. During periods of proliferation (ie, puberty, estrus and pregnancy), which are stimulated by ovarian hormones, TGF-beta 1 activation decreased in some cells, consistent with preparation for proliferation. Paradoxically, other cells simultaneously increase TGF-beta 1 immunoreactivity, which suggests that TGF-beta 1 differentially restrains epithelial subpopulations from responding to hormonal signals to proliferate. These data suggest that endogenous TGF-beta 1 activation and thus activity are regulated by ovarian hormones. To determine the specific consequences of TGF-beta 1 activity, we manipulated TGF-beta 1 levels in vivo using Tgfbeta 1 knockout mice and undertook tissue recombination experiments with heterozygous tissue. In Tgfbeta 1 heterozygous mice, which have <10% wild-type levels of TGF-beta1, ductal development during puberty and alveolar development during pregnancy were accelerated, consistent with its role as a growth inhibitor. The proliferative index of Tgfbeta 1+/- epithelium was increased approximately twofold in quiescent tissue and fourfold in proliferating tissue but both ducts and alveoli were grossly and histologically normal. To test whether epithelial TGF-beta1 was critical to the proliferative phenotype, Tgfbeta 1+/+ and +/- epithelium were transplanted into +/+ mammary stroma. The outgrowth of Tgfbeta 1+/- epithelium was accelerated in wild-type hosts, indicating that the phenotype was intrinsic to the epithelium. Moreover, proliferation was 15-fold greater in Tgfbeta 1+/- than wild-type mice after ovariectomy and treatment with estrogen and progesterone, suggesting that TGF-beta 1 acts in an autocrine or juxtacrine manner to regulate epithelial proliferation. Together these data indicate that ovarian hormones regulate TGF-beta 1 activation, which in turn restricts proliferative response to hormone signaling.
转化生长因子β1(TGF-β1)是一种多能细胞因子,它可以抑制上皮细胞增殖并诱导细胞凋亡,但也广泛参与乳腺癌的进展。了解其在乳腺发育中的生物学作用对于理解其在癌症中的作用至关重要。TGF-β1以潜伏复合物的形式产生,在与受体结合之前需要细胞外激活。为了更好地理解其在乳腺发育过程中作用的时空调节,我们使用选择区分潜伏性和活性TGF-β的抗体原位检测激活模式。激活受到高度限制。TGF-β1激活主要定位于上皮细胞,在上皮细胞内,它仅限于腔上皮细胞,而帽状细胞或肌上皮细胞中不存在。在腔上皮细胞内,我们注意到进一步的限制。在由卵巢激素刺激的增殖期(即青春期、发情期和妊娠期),一些细胞中的TGF-β1激活减少,这与增殖准备一致。矛盾的是,其他细胞同时增加TGF-β1免疫反应性,这表明TGF-β1以不同方式抑制上皮亚群对激素信号的增殖反应。这些数据表明内源性TGF-β1激活以及活性受卵巢激素调节。为了确定TGF-β1活性的具体后果,我们使用Tgfbeta 1基因敲除小鼠在体内操纵TGF-β1水平,并使用杂合组织进行组织重组实验。在Tgfbeta 1杂合小鼠中,其TGF-β1水平低于野生型水平的10%,青春期的导管发育和妊娠期的腺泡发育加速,这与其作为生长抑制剂的作用一致。在静止组织中,Tgfbeta 1+/-上皮细胞的增殖指数增加约两倍,在增殖组织中增加四倍,但导管和腺泡在大体和组织学上均正常。为了测试上皮TGF-β1对增殖表型是否至关重要,将Tgfbeta 1+/+和+/-上皮细胞移植到+/+乳腺基质中。Tgfbeta 1+/-上皮细胞在野生型宿主中的生长加速,表明该表型是上皮细胞固有的。此外,卵巢切除并用雌激素和孕酮处理后,Tgfbeta 1+/-小鼠的增殖比野生型小鼠高15倍,这表明TGF-β1以自分泌或旁分泌方式调节上皮细胞增殖。这些数据共同表明卵巢激素调节TGF-β1激活,进而限制对激素信号的增殖反应。