Itoi M, Amagai T
Department of Immunology and Microbiology, Meiji University of Oriental Medicine, Kyoto, Japan.
Cell Immunol. 1998 Jan 10;183(1):32-41. doi: 10.1006/cimm.1998.1239.
Previously, we have shown that embryonic day 12 thymus anlage cultured alone cannot develop into the mature organ but degenerates. In the present study, we investigated the cause of this insufficient organogenesis of embryonic day 12 thymus anlage in organ culture. We cocultured embryonic day 12 thymus anlages with various cell lines as pellets formed by centrifugation. In coculture with fibroblastic cell lines, but not with thymic epithelial cell lines, embryonic day 12 thymus anlages developed to support full T cell differentiation, and expressed mature stromal cell markers, Ia and Kb. By pellet culture of thymus anlages and fibroblastic cell lines transfected with a beta-galactosidase expression vector, we analyzed the distribution of added fibroblastic cells in pellets. The added fibroblastic cells constituted neither thymic capsule nor septa but disappeared after about 2 weeks in culture. Moreover, immunohistochemical studies indicated that added fibroblastic cells were adjacent to mesenchymal cells of thymus anlage. Our results strongly suggest that added fibroblastic cells support the development of the thymus anlage through interaction with its mesenchymal cells.
此前,我们已经表明,单独培养的胚胎第12天胸腺原基无法发育成成熟器官,而是会退化。在本研究中,我们调查了器官培养中胚胎第12天胸腺原基器官发生不足的原因。我们将胚胎第12天胸腺原基与通过离心形成的各种细胞系小丸共同培养。与成纤维细胞系共同培养时,胚胎第12天胸腺原基能够发育以支持完整的T细胞分化,并表达成熟的基质细胞标志物Ia和Kb,但与胸腺上皮细胞系共同培养时则不能。通过对转染了β-半乳糖苷酶表达载体的胸腺原基和成纤维细胞系进行小丸培养,我们分析了添加的成纤维细胞在小丸中的分布情况。添加的成纤维细胞既不构成胸腺被膜也不构成间隔,而是在培养约2周后消失。此外,免疫组织化学研究表明,添加的成纤维细胞与胸腺原基的间充质细胞相邻。我们的结果强烈表明,添加的成纤维细胞通过与其间充质细胞相互作用来支持胸腺原基的发育。