Roberts V J, Bentley C A, Guo Q, Matzuk M M, Woodruff T K
Department of Reproductive Medicine, University of California, San Diego, La Jolla 92093-0674, USA.
Endocrinology. 1996 Oct;137(10):4201-9. doi: 10.1210/endo.137.10.8828478.
Activin affects the growth and differentiation of many cultured cell types, including rat anterior pituitary cells and gonadal and neuronal cell lines. Endogenous activins regulate mesoderm induction, body axis formation, and organogenisis in the developing embryo. The messenger RNAs encoding inhibin/activin subunits, follistatin (an activin-binding protein), and activin type II receptors (ActRII and IIB) are expressed in various cell types and tissues of the embryonic rat and mouse. Follistatin-deficient mice have numerous embryonic defects, including shiny taut skin, allowing relatively easy identification by the later stages of embryogenesis. ActRII-deficient mice, on the other hand, show limited developmental defects, with some (22%) embryonic day 18.5 (E18.5) ActRII-deficient embryos showing various skeletal and facial abnormalities. The present study was undertaken to identify the target tissues for biologically active activin A and assess the significance of its association with ActRII and follistatin in developing rat and mouse embryos. Fresh-frozen, slide-mounted, rat (E13 to E19) and mouse (E18.5) embryo sections were incubated with 125I-labeled recombinant human activin A. Nonspecific binding was evaluated by competition with an excess of cold activin A. As determined by image analysis, the highest levels of activin A binding were observed throughout the brain, spinal cord, and trigeminal and spinal ganglia at all ages. Lower levels of binding were found in the dermis of the skin starting on E15. Follistatin-deficient mice demonstrated similar patterns and levels of activin A binding in the neural tissues compared to wild-type controls, but binding was absent in the skin. In ActRII-deficient mice, activin A binding was completely absent in neural tissues, but was similar to wild-type control levels in the dermal layer of the skin. The data indicate that activin A binds to specific tissues of mouse and rat embryos and that binding is dependent upon the presence of ActRII in the central and peripheral nervous system and on follistatin in the skin.
激活素影响多种培养细胞类型的生长和分化,包括大鼠垂体前叶细胞以及性腺和神经细胞系。内源性激活素在发育中的胚胎中调节中胚层诱导、体轴形成和器官发生。编码抑制素/激活素亚基、卵泡抑素(一种激活素结合蛋白)和激活素II型受体(ActRII和IIB)的信使核糖核酸在胚胎大鼠和小鼠的各种细胞类型和组织中表达。卵泡抑素缺陷型小鼠有许多胚胎缺陷,包括皮肤紧绷发亮,在胚胎发育后期相对容易识别。另一方面,ActRII缺陷型小鼠表现出有限的发育缺陷,一些(22%)胚胎第18.5天(E18.5)的ActRII缺陷型胚胎出现各种骨骼和面部异常。本研究旨在确定生物活性激活素A的靶组织,并评估其在发育中的大鼠和小鼠胚胎中与ActRII和卵泡抑素关联的意义。将新鲜冷冻、载玻片固定的大鼠(E13至E19)和小鼠(E18.5)胚胎切片与125I标记的重组人激活素A孵育。通过与过量冷激活素A竞争来评估非特异性结合。通过图像分析确定,在所有年龄段,整个大脑、脊髓、三叉神经节和脊髓神经节中观察到的激活素A结合水平最高。从E15开始,在皮肤真皮中发现较低的结合水平。与野生型对照相比,卵泡抑素缺陷型小鼠在神经组织中表现出相似的激活素A结合模式和水平,但在皮肤中没有结合。在ActRII缺陷型小鼠中,神经组织中完全没有激活素A结合,但在皮肤真皮层中与野生型对照水平相似。数据表明,激活素A与小鼠和大鼠胚胎的特定组织结合,并且这种结合取决于中枢和外周神经系统中ActRII的存在以及皮肤中卵泡抑素的存在。