Wilson D B, Finta L A, Center E M, Paavola L G
Virchows Arch B Cell Pathol Incl Mol Pathol. 1982;39(1):101-10. doi: 10.1007/BF02892840.
Abnormalities of notochordal cells and of mesenchymal cells in embryos of Danforth's short-tail (Sd) and C57BL mice were examined by means of electron microscopy and cytochemical staining at 11.0 and 11.5 days of gestation. In abnormal (Sd/+; Sd/Sd) embryos, the notochordal cells were markedly deficient in bundles of filaments and lacked surface protrusions, and the notochordal basal lamina was continuous; in contrast, notochordal cells of normal (+/+) littermates and of C57BL embryos contained numerous bundles of filaments and showed fingerlike surface protrusions and discontinuous basal laminae. The pathologic notochordal cells also lacked the accumulations of glycogen revealed in the normals by means of thiocarbohydrazide cytochemical staining at the electron microscopic level. The mesenchymal cells of abnormals also were deficient in filaments but did stain for glycogen, though less prominently than did normal mesenchymal cells.
在妊娠11.0天和11.5天时,通过电子显微镜和细胞化学染色检查了丹佛短尾(Sd)小鼠和C57BL小鼠胚胎中脊索细胞和间充质细胞的异常情况。在异常(Sd/+; Sd/Sd)胚胎中,脊索细胞明显缺乏丝状束,且没有表面突起,脊索基膜是连续的;相比之下,正常(+/+)同窝小鼠和C57BL胚胎的脊索细胞含有大量丝状束,并呈现出指状表面突起和不连续的基膜。通过电子显微镜水平的硫代碳酰肼细胞化学染色发现,病理状态下的脊索细胞也缺乏正常细胞中糖原的积累。异常胚胎的间充质细胞也缺乏丝状束,但能对糖原进行染色,不过染色程度不如正常间充质细胞明显。