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用Y染色体探针原位杂交研究无骨膜跖骨与造血细胞共培养体系中破骨细胞的发育。

Osteoclast development in the coculture system of periostless metatarsal bones and hemopoietic cells studied by in situ hybridization with a probe for Y chromosomes.

作者信息

Hagenaars C E, Kawilarang-de Haas E W, Hazekamp J, Wiegant J, Nijweide P J

机构信息

Laboratory of Cell Biology and Histology, University of Leiden, The Netherlands.

出版信息

Calcif Tissue Int. 1994 Feb;54(2):170-4. doi: 10.1007/BF00296070.

Abstract

In the coculture system of periostless metatarsal bones of 17-day-old fetal mice and osteoclast progenitors, osteoclasts will develop. Our goal in the present report was to provide further evidence that in the coculture system of fetal metatarsal bone rudiments with hemopoietic cells, the osteoclasts developing inside the bone rudiments are exclusively derived from the cells suspended in the plasma clot and not from endogenous precursor cells of the bone explants themselves, by using the technique of in situ hybridization with a probe for the mouse Y chromosome. Osteoclast formation in unstripped male metatarsal rudiments, occurring after 3-4 days of culture, was compared with osteoclast formation in cocultures of female metatarsal rudiments and male bone marrow cells, occurring after 5-6 days of culture. Osteoclasts were recognized by their tartrate-resistant acid phosphatase activity. In paraffin sections of cultured male metatarsals, the mean percentage of microscopically identifiable osteoclast nuclei, in which the Y chromosome could be detected, was 43.1 +/- 4.2% (n = 12). For cocultures of female metatarsal bones and male bone marrow cells this mean percentage was 40.9 +/- 5.7% (n = 17). Statistical comparison by means of the two sample t-test indicated no significant difference in the percentages of osteoclast nuclei containing the Y chromosome for both groups. We concluded that the osteoclasts do derive from cocultured cells and not from precursor cells in the bone explant itself.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在17日龄胎鼠无骨膜跖骨与破骨细胞祖细胞的共培养体系中,会形成破骨细胞。在本报告中,我们的目标是通过使用针对小鼠Y染色体的探针进行原位杂交技术,进一步证明在胎儿跖骨雏形与造血细胞的共培养体系中,在骨雏形内部形成的破骨细胞完全来源于悬浮在血浆凝块中的细胞,而非来自骨外植体自身的内源性前体细胞。将未剥离的雄性跖骨雏形培养3 - 4天后形成破骨细胞的情况,与雌性跖骨雏形和雄性骨髓细胞共培养5 - 6天后形成破骨细胞的情况进行比较。通过抗酒石酸酸性磷酸酶活性来识别破骨细胞。在培养的雄性跖骨的石蜡切片中,显微镜下可识别出能检测到Y染色体的破骨细胞核的平均百分比为43.1±4.2%(n = 12)。对于雌性跖骨和雄性骨髓细胞的共培养,该平均百分比为40.9±5.7%(n = 17)。通过两样本t检验进行的统计比较表明,两组中含有Y染色体的破骨细胞核百分比无显著差异。我们得出结论,破骨细胞确实来源于共培养的细胞,而非来自骨外植体自身的前体细胞。(摘要截断于250字)

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