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991.
The fine structure of developing cartilage is described in the area of the future vertebral bodies in the cervical region of chick embryos. Incubation ages range from 36 hours, when the sclerotome of the somite begins to break up, to the thirteenth day. In the 36- to 72-hour interval cells of the sclerotome become free and assume stellate form. Polyribosomes nearly fill the largely undifferentiated cytoplasm. Microfibrils and amorphous material appear in the connective tissue space 1 The extent of the connective tissue space is determined by boundary (basement) membranes; externally by those of epithelium facing the geometric exterior of the organism and internally by those of endothelium, mesothelium, muscle, nerve and fat. The true contents of the connective tissue space are the connective tissues. As used in this paper “connective tissue space” refers to the extracellular portion, in which the fibrous and amorphous components exist. by the end of the third day. From the fourth through the sixth day both cellular contours and contents suggest fibroblasts. Microfibrillar diameter increases from 50 to 150 Å. Periodicity does not occur. Matrix granules appear and establish contact with microfibrils. From the eighth through the eleventh day the predominating cell types are chondroblasts and chondrocytes whose fine structure is typical. Microfibrils become more numerous and matrix granules larger. During days 11 through 13, chondrocytes show degenerative changes including lucid areas of nucleoplasm and cytoplasm with fragmentation of endoplasmic reticulum. Microfibrils and matrix granules are heavily concentrated in the connective tissue space and lucent osteoid appears. 相似文献
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A. F. Henschen I. Strömberg M. Bygdeman D. Dahl B. Hoffer Å. Seiger I. Olson 《Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale》1989,75(2):317-326
Summary Human fetal spinal cord tissue was recovered from elective abortions and grafted to the anterior chamber of the eye of adult athymic nude rats. The transplants slowly became vascularized from the host iris during the first months. There was a clear cut stage-dependent survival and growth along a more human time-table. Fetal spinal cord tissue from embryos younger than gestational week 8 showed a much better survival and growth than tissue from older stages. Using laminin immunohistochemistry blood vessels could be visualized in the grafts. The pattern of vascularization was, however, clearly abnormal; there were fewer vessels which had abnormally thick walls as compared to those in the normal spinal cord. Similar to rat spinal cord allografts the human spinal cord xenografts displayed a relative gliosis and were surrounded by a glial layer visualized with antibodies against glial fibrillary acidic protein. Neurofilament-immunoreactive fibres were found inside the glial layer. A variety of neurons were found including large polygonal motoneuron-shaped cells, albeit with CGRP and AChE negative cell bodies. Both Substance P and enkepha-lin-immunoreactive cells and fibres were found. It is concluded that xenografted fetal human spinal cord survives, grows and may provide a useful model for experimental studies of human spinal cord development and connectivity. 相似文献
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James M. Olson Wakelin McNeel Anne B. Young William R. Mancini 《Journal of neuro-oncology》1992,13(1):35-42
Subcellular fractionation was performed on human U251 glioblastoma cultures. In all subcellular fractions, the binding of the peripheral benzodiazepine ligand, [3H]PK 11195, correlated with the specific activity of monoamine oxidase (r = 0.95, p < 0.001) and succinate dehydrogenase (r = 0.93, p < 0.001), two mitochondrial enzymes. The specific activity of plasma membrane and nuclear markers correlated poorly with the presence of PK 11195 binding sites. These data support the mitochondrion as the primary location of peripheral-type benzodiazepine binding sites (PBBS) in human glioma cells.Mitochondria-rich preparations were then assayed for [3H]Ro5-4964 binding. Six nM [3H]Ro5-4964 failed to specifically bind to human U251 mitochondria, but bound vigorously to mitochondria from rat C6 glioma. These data indicate that the low affinity of Ro5-4864 for PBBS in human glioma cells compared to those in rat is due to interspecies receptor variation rather than impaired drug transport into human cells. 相似文献
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E F Pierce N W Eastman R W McGowan H Tripathi W L Dewey K G Olson 《British journal of sports medicine》1994,28(3):164-166
Previous research investigating the response of plasma beta-endorphins (beta-EP) to resistance exercise has resulted in equivocal findings. To examine further the effects of resistance exercise on beta-EP immunoreactivity, 10 male and 10 female college-age students participated in a series of controlled isotonic resistance exercises. The session consisted of three sets of eight repetitions at 80% of one repetition maximum (1-RM) for each of the following exercises: (1) bench press; (2) lateral pull-downs; (3) seated arm curls; and (4) military press. Blood plasma was sampled both before and after the lifting routine and beta-endorphin levels were determined by radioimmunoassay. A Students t test for paired samples indicated that mean(s.e.) plasma beta-endorphin levels after exercise (10.5(1.3) pg beta-EP ml-1) were significantly decreased as compared with pre-exercise (control) levels (16.5(1.2), P < 0.05). While the mechanism(s) contributing to the decrease in immunoreactivity is unclear, it may be the result of the synergistic effect of beta-EP clearance during rest intervals and changes in psychological states between sampling. 相似文献