Ramachandran R K, Govindarajan V, Seid C A, Patil S, Tomlinson C R
Department of Biology, University of Houston, Texas 77204-5513, USA.
Dev Dyn. 1995 Sep;204(1):77-88. doi: 10.1002/aja.1002040110.
The mechanisms underlying sea urchin gastrulation and spiculogenesis have been sought for decades. We have identified two growth factor signaling pathways that are involved in these developmental events. Antibodies against mammalian platelet-derived growth factor (PDGF) receptor-beta inhibited gastrulation and spiculogenesis, and antibodies against human epidermal growth factor (EGF) receptor disrupted gastrulation and spicule placement in Lytechinus pictus and L. variegatus embryos. Our studies suggested that the antibodies affect development by inhibiting rather than activating the signaling pathways. Polyclonal and monoclonal antibodies against the mammalian receptors recognized specifically Lytechinus proteins of the expected size of 170-180 x 10(3) M(r). Growth factor binding assays indicated that there are approximately 1.25 x 10(4) platelet-derived growth factor-like receptors per cell at the mesenchyme blastula stage of L. pictus, and human platelet-derived growth factor bound with an apparent affinity of KD = 4.4 nM to dissociated cells at the mesenchyme blastula stage. Immunolabelling experiments showed that at the gastrula stage, the Lytechinus platelet-derived growth factor-like receptors are located on the primary mesenchyme cells, the gut, and most prominently on the secondary mesenchyme cells and the stomodeum. The epidermal growth factor-like receptors stained less intensely on the gut and primary and secondary mesenchyme cells. Both receptors are expressed on the ciliary band and the gut of the pluteus larva but only the PDGF-like receptor is expressed on the primary mesenchyme cells. Pulse studies showed that the embryos are sensitive to the platelet-derived growth factor receptor-beta and epidermal growth factor receptor antibodies from the blastula to sometime between the mesenchyme blastula and midgastrula stages. We show that antibodies enter the blastocoel as late as the gastrula stage. Our results suggest that platelet-derived growth factor-like and epidermal growth factor-like signaling pathways are involved in the early differentiation and morphogenesis of the sea urchin gut and spicules.
几十年来,人们一直在探寻海胆原肠胚形成和骨针形成的潜在机制。我们已经鉴定出两条参与这些发育过程的生长因子信号通路。针对哺乳动物血小板衍生生长因子(PDGF)受体β的抗体抑制了原肠胚形成和骨针形成,而针对人表皮生长因子(EGF)受体的抗体则破坏了花斑海胆和多变海胆胚胎的原肠胚形成及骨针定位。我们的研究表明,这些抗体通过抑制而非激活信号通路来影响发育。针对哺乳动物受体的多克隆和单克隆抗体特异性识别预期大小为170 - 180×10³ M(r)的花斑海胆蛋白。生长因子结合试验表明,在花斑海胆间充质囊胚阶段每个细胞约有1.25×10⁴个血小板衍生生长因子样受体,人血小板衍生生长因子以KD = 4.4 nM的表观亲和力与间充质囊胚阶段的解离细胞结合。免疫标记实验表明,在原肠胚阶段,花斑海胆血小板衍生生长因子样受体位于初级间充质细胞、肠道上,最显著的是位于次级间充质细胞和口凹处。表皮生长因子样受体在肠道、初级和次级间充质细胞上的染色强度较低。两种受体都在长腕幼虫的纤毛带和肠道上表达,但只有血小板衍生生长因子样受体在初级间充质细胞上表达。脉冲研究表明,胚胎从囊胚期到间充质囊胚期和原肠胚中期之间的某个时间对血小板衍生生长因子受体β和表皮生长因子受体抗体敏感。我们发现抗体最晚在原肠胚阶段进入囊胚腔。我们的结果表明,血小板衍生生长因子样和表皮生长因子样信号通路参与海胆肠道和骨针的早期分化和形态发生。