Zhong Aimei, Wang Guohua, Yang Jie, Xu Qijun, Yuan Quan, Yang Yanqing, Xia Yun, Guo Ke, Horch Raymund E, Sun Jiaming
Department of Plastic Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
J Cell Mol Med. 2014 Jul;18(7):1257-66. doi: 10.1111/jcmm.12275. Epub 2014 Apr 10.
True macromastia is a rare but disabling condition characterized by massive breast growth. The aetiology and pathogenic mechanisms for this disorder remain largely unexplored because of the lack of in vivo or in vitro models. Previous studies suggested that regulation of epithelial cell growth and development by oestrogen was dependent on paracrine growth factors from the stroma. In this study, a co-culture model containing epithelial and stromal cells was used to investigate the interactions of these cells in macromastia. Epithelial cell proliferation and branching morphogenesis were measured to assess the effect of macromastic stromal cells on epithelial cells. We analysed the cytokines secreted by stromal cells and identified molecules that were critical for effects on epithelial cells. Our results indicated a significant increase in cell proliferation and branching morphogenesis of macromastic and non-macromastic epithelial cells when co-cultured with macromastic stromal cells or in conditioned medium from macromastic stromal cells. Hepatocyte growth factor (HGF) is a key factor in epithelial-stromal interactions of macromastia-derived cell cultures. Blockade of HGF with neutralizing antibodies dramatically attenuated epithelial cell proliferation in conditioned medium from macromastic stromal cells. The epithelial-stromal cell co-culture model demonstrated reliability for studying interactions of mammary stromal and epithelial cells in macromastia. In this model, HGF secreted by macromastic stromal cells was found to play an important role in modifying the behaviour of co-cultured epithelial cells. This model allows further studies to investigate basic cellular and molecular mechanisms in tissue from patients with true breast hypertrophy.
真性巨乳症是一种罕见但致残的疾病,其特征为乳房大量增生。由于缺乏体内或体外模型,这种疾病的病因和发病机制在很大程度上仍未得到探索。先前的研究表明,雌激素对上皮细胞生长和发育的调节依赖于来自基质的旁分泌生长因子。在本研究中,使用包含上皮细胞和基质细胞的共培养模型来研究这些细胞在巨乳症中的相互作用。测量上皮细胞增殖和分支形态发生,以评估巨乳症基质细胞对上皮细胞的影响。我们分析了基质细胞分泌的细胞因子,并鉴定了对上皮细胞有影响的关键分子。我们的结果表明,当与巨乳症基质细胞共培养或在巨乳症基质细胞的条件培养基中培养时,巨乳症和非巨乳症上皮细胞的细胞增殖和分支形态发生均显著增加。肝细胞生长因子(HGF)是巨乳症来源细胞培养物上皮-基质相互作用中的关键因子。用中和抗体阻断HGF可显著减弱巨乳症基质细胞条件培养基中的上皮细胞增殖。上皮-基质细胞共培养模型证明了在研究巨乳症中乳腺基质细胞和上皮细胞相互作用方面的可靠性。在该模型中,发现巨乳症基质细胞分泌的HGF在改变共培养上皮细胞的行为中起重要作用。该模型允许进一步研究以探究真性乳腺肥大患者组织中的基本细胞和分子机制。