Bode K, Hofmann H D, Müller T H, Otten U, Schmidt R, Unsicker K
Brain Res. 1986 Jun;392(1-2):139-50. doi: 10.1016/0165-3806(86)90240-3.
Whether or not adrenal medullary (chromaffin) cells which respond to nerve growth factor (NGF) both in vitro and in vivo require NGF for their normal development is controversial. Systemic deprivation of endogenous NGF by injection of anti-NGF antibodies into rat fetuses or by transfer of anti-NGF to the offspring of autoimmunized mothers has provided conflicting results. We have reinvestigated the effects of a specific antiserum to NGF on the morphology, catecholamine (CA) and neuropeptide (Met-enkephalin, Met-ENK; substance P, SP) content, and choline acetyltransferase (ChAT) activity of the rat adrenal medulla. Fetuses were injected with anti-NGF antibodies on day 17 of gestation and postnatally at daily intervals for 7 days. The histological appearance of adrenal medullae of anti-NGF injected animals was not altered as compared to controls. Ultrastructurally, no degenerative changes or developmental retardation of chromaffin cells could be detected. However, numbers of chromaffin granules per micron 2 of cytoplasmic area were greater and the mean diameters of the cores of adrenaline storage granules were smaller in antibody-treated than in control animals. CA and SP content, ratios of adrenaline to noradrenaline and ChAT activities were identical in anti-NGF-treated and control animals. Anti-NGF antibodies caused a reduction of adrenal Met-ENK by 40% as compared to controls. Superior cervical ganglia from the same animals were used to document immunosympathectomy induced by the antiserum. They displayed the well-established structural alterations and a marked reduction of the CA content. We conclude that administration of anti-NGF antibodies to embryonic and early postnatal rats induces only subtle changes in the ultramorphology of chromaffin cells without altering the development of normal CA levels. The small, yet significant effects of anti-NGF antibodies on adrenal Met-ENK, however, may suggest a role for endogenous NGF in the regulation of opioid peptide metabolism in developing chromaffin cells.
肾上腺髓质(嗜铬)细胞在体外和体内均对神经生长因子(NGF)产生反应,但其正常发育是否需要NGF仍存在争议。通过向大鼠胎儿注射抗NGF抗体或向自身免疫母亲的后代转移抗NGF来系统性剥夺内源性NGF,结果相互矛盾。我们重新研究了针对NGF的特异性抗血清对大鼠肾上腺髓质的形态、儿茶酚胺(CA)和神经肽(甲硫氨酸脑啡肽,Met-ENK;P物质,SP)含量以及胆碱乙酰转移酶(ChAT)活性的影响。在妊娠第17天给胎儿注射抗NGF抗体,并在出生后每天注射一次,持续7天。与对照组相比,注射抗NGF动物的肾上腺髓质组织学外观未改变。在超微结构上,未检测到嗜铬细胞的退行性变化或发育迟缓。然而,与对照动物相比,抗体处理动物每平方微米细胞质区域的嗜铬颗粒数量更多,肾上腺素储存颗粒核心的平均直径更小。抗NGF处理组和对照组动物的CA和SP含量、肾上腺素与去甲肾上腺素的比率以及ChAT活性相同。与对照组相比,抗NGF抗体使肾上腺Met-ENK减少了40%。使用同一动物的颈上神经节来证明抗血清诱导的免疫交感神经切除术。它们表现出公认的结构改变和CA含量的显著降低。我们得出结论,向胚胎期和出生后早期的大鼠施用抗NGF抗体仅在嗜铬细胞的超微形态上引起细微变化,而不改变正常CA水平的发育。然而,抗NGF抗体对肾上腺Met-ENK的微小但显著的影响可能表明内源性NGF在发育中的嗜铬细胞中阿片肽代谢调节中起作用。