Crowley M R, Head K L, Kwiatkowski D J, Asch H L, Asch B B
Division of Experimental Pathology, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, New York 14263, USA.
Dev Biol. 2000 Sep 15;225(2):407-23. doi: 10.1006/dbio.2000.9844.
Gelsolin is an actin-binding/severing protein expressed in intracellular and secreted forms. It is a major regulator of the form and function of the actin cytoskeleton in most all cells. Here we demonstrate that female mice with a targeted deletion of the gelsolin gene (Gsn-/-) have defects in mammary gland morphogenesis. Two distinct defects were identified in the gelsolin-null mammary gland. First, the mammary anlage from Gsn-/- mice failed to elongate at the onset of puberty and remained rudimentary until approximately 9 weeks of age, early block (Gsn-/-(EB)). Second, after the mammary epithelium had filled the mammary fat pad, a complete lack of terminal branching, or late block, was observed (Gsn-/-(LB)). The Gsn-/-(EB) was seen in 70% of Gsn-/- mice and appeared to be dependent on a modifier gene(s) in addition to the loss of gelsolin. Gsn-/-(LB) was observed in all Gsn-/- mice. Terminal end buds (TEBs) were not evident in the mammary anlage from Gsn-/-(EB) mice until approximately 9 weeks of age. Cellular proliferation in the terminal ductal regions of Gsn-/-(EB) females was detected by bromodeoxyuridine incorporation, but was less than that found in the TEBs of age-matched controls. In mice deficient for gelsolin, mammary gland architecture was unaltered at the histological level. Lobuloalveolar development was delayed in response to pregnancy in mammary glands of Gsn-/- mice but was otherwise normal. Lactation and involution in the gelsolin-null animals were similar to those of wild-type mice. Transplantation of epithelium devoid of gelsolin into a wild-type (GsnWT) mammary fat pad resulted in proper arborization of the ductal tree. Transplantation of GsnWT epithelium into the Gsn-/- fat pad recapitulated the lack of terminal branching seen in Gsn-/- females. These results indicate that gelsolin is required in the mammary stroma for proper ductal morphogenesis. Our results provide the first evidence of an actin regulatory protein affecting mammary ductal growth through stromal-epithelial communication.
凝溶胶蛋白是一种以细胞内和分泌形式表达的肌动蛋白结合/切割蛋白。它是大多数细胞中肌动蛋白细胞骨架形态和功能的主要调节因子。在此我们证明,凝溶胶蛋白基因靶向缺失的雌性小鼠(Gsn-/-)在乳腺形态发生方面存在缺陷。在凝溶胶蛋白缺失的乳腺中发现了两种不同的缺陷。首先,Gsn-/-小鼠的乳腺原基在青春期开始时未能伸长,直到大约9周龄时仍处于未发育状态,即早期阻滞(Gsn-/-(EB))。其次,在乳腺上皮填充乳腺脂肪垫后,观察到完全缺乏终末分支,即晚期阻滞(Gsn-/-(LB))。70%的Gsn-/-小鼠出现Gsn-/-(EB),似乎除了凝溶胶蛋白缺失外,还依赖于一个修饰基因。所有Gsn-/-小鼠均观察到Gsn-/-(LB)。直到大约9周龄,Gsn-/-(EB)小鼠的乳腺原基中才出现明显的终末芽(TEB)。通过溴脱氧尿苷掺入检测到Gsn-/-(EB)雌性小鼠终末导管区域的细胞增殖,但低于年龄匹配对照组TEB中的增殖。在凝溶胶蛋白缺陷的小鼠中,乳腺结构在组织学水平上未发生改变。Gsn-/-小鼠乳腺中的小叶腺泡发育在妊娠时延迟,但其他方面正常。凝溶胶蛋白缺失动物的泌乳和退化与野生型小鼠相似。将不含凝溶胶蛋白的上皮移植到野生型(GsnWT)乳腺脂肪垫中,导致导管树正常分支。将GsnWT上皮移植到Gsn-/-脂肪垫中,重现了Gsn-/-雌性小鼠中缺乏终末分支的现象。这些结果表明,凝溶胶蛋白在乳腺基质中是导管正常形态发生所必需的。我们的结果首次证明了一种肌动蛋白调节蛋白通过基质-上皮通讯影响乳腺导管生长。