Frenkel S R, Guerra L A, Mitchell O G, Singh I J
Department of Anatomy, New York University Dental Center, NY 10010.
Cell Tissue Res. 1990 May;260(3):507-11. doi: 10.1007/BF00297230.
This study demonstrates, via immunohistochemistry and bioassay, the presence of NGF in embryonic bone and cartilage of the chick. Embryos were killed on days 6-9 of incubation at 12 h intervals, and on days 10-18 at 24 h intervals. Paraffin-embedded sections of hind limbs or buds were immunostained with a polyclonal antibody against NGF and the biotin-avidin-horseradish peroxidase technique. Immunostaining was positive in both bone and cartilage, with cartilage staining more intensely. For bioassay, bones from the hind limbs of 9- and 12-day embryos were fast-frozen, lyophilized, and homogenized with Medium 199 (M199). Dorsal root ganglia from 8-day embryos were cultured for 24-36 h with rooster plasma, M199, and varying concentrations of bone homogenate. Significant neurite outgrowth was seen, with the greatest response elicited by 12-day bone homogenate. Addition of anti-NGF to the cultures abolished neurite outgrowth. The results indicate that NGF is present in cartilage and bone of the chick embryo; it may determine the density of sympathetic innervation to the developing skeletal tissues.
本研究通过免疫组织化学和生物测定法,证实了鸡胚胎的骨和软骨中存在神经生长因子(NGF)。在孵化的第6至9天,每隔12小时处死胚胎;在第10至18天,每隔24小时处死胚胎。用抗NGF多克隆抗体和生物素-抗生物素蛋白-辣根过氧化物酶技术对后肢或芽的石蜡包埋切片进行免疫染色。骨和软骨的免疫染色均呈阳性,软骨染色更强烈。用于生物测定时,将9日龄和12日龄胚胎后肢的骨头速冻、冻干,并用199培养基(M199)匀浆。将8日龄胚胎的背根神经节与公鸡血浆、M199以及不同浓度的骨匀浆一起培养24至36小时。观察到明显的神经突生长,其中12日龄骨匀浆引起的反应最强。向培养物中添加抗NGF可消除神经突生长。结果表明,NGF存在于鸡胚胎的软骨和骨中;它可能决定发育中骨骼组织的交感神经支配密度。