Wilson D B, Wyatt D P
Acta Neuropathol. 1986;70(2):142-8. doi: 10.1007/BF00691432.
The cytochemical localization of acid phosphatase (AP) was studied at the ultrastructural level in the abnormal neuroepithelium of dysraphic loop-tail (Lp/Lp) embryos between 9 and 12 days of gestation. At 9-11 days, normal and abnormal embryos showed a positive AP reaction throughout the thickness of the neuroepithelium, i.e., in apical, intermediate, and basal zones, although many cells were unreactive. The reaction is sensitive to sodium fluoride and occurs in saccules and vesicles associated with the Golgi complex, as well as in vacuoles of varying size containing flocculent and particulate material. Gap-junctional vesicles, which are known to occur in increased numbers in abnormal brains, were AP-negative. By 12 days of gestation, the reaction in normal embryos was localized in the midventral marginal layer, where some cell processes were filled with reaction product; in abnormal embryos, these AP-positive processes were not observed. The results indicate that perturbations in lysosomal activity may not be fundamentally involved in the etiology of dysraphism in this mutant.
在妊娠9至12天的脊柱裂环尾(Lp/Lp)胚胎异常神经上皮中,在超微结构水平上研究了酸性磷酸酶(AP)的细胞化学定位。在9至11天,正常和异常胚胎的神经上皮全层均显示出阳性AP反应,即在顶端、中间和基底区域,尽管许多细胞无反应。该反应对氟化钠敏感,发生在与高尔基体相关的小囊泡和囊泡中,以及含有絮状和颗粒物质的大小不一的液泡中。已知在异常大脑中数量增加的缝隙连接囊泡为AP阴性。到妊娠12天时,正常胚胎中的反应定位于腹中缘层,其中一些细胞突起充满反应产物;在异常胚胎中,未观察到这些AP阳性突起。结果表明,溶酶体活性的扰动可能在该突变体脊柱裂的病因学中并非根本因素。