Sydora B C, Habu S, Taniguchi M
Center for Neurobiology and Molecular Immunology, School of Medicine, Chiba University, Japan.
Int Immunol. 1993 Jul;5(7):743-51. doi: 10.1093/intimm/5.7.743.
We have used C.B-17 severe combined immune deficiency (SCID) mice to study the repopulation of intestinal intraepithelial cells in these mice. We have found that intestinal intraepithelial lymphocytes (IELs) injected into SCID mice preferentially repopulate the intestinal epithelium. About 5 weeks after injection we can detect significant numbers of IEL in repopulated SCID mice. Repopulation occurs in approximately 70% of the injected mice and the amount of recovered cells per mouse is variable. The recovered cells are of donor-type origin and exhibit a typical IEL phenotype. The donor-type T lymphocytes that can sometimes be found in other organs of IEL-repopulated SCID mice are generally of low number. They are not stained with antibodies against IEL-specific markers and their phenotypes appear to be more typical for T cells normally found in these sites. In contrast, the intestinal epithelium of SCID mice cannot be efficiently repopulated with lymphocytes using cells of other organs including thymocytes, Peyer's patch lymphocytes, and bone marrow cells. From our data we conclude that intestinal IELs are confined to the intestinal epithelium and possibly contain a precursor-type cell that preferentially regenerates cells of its own population.
我们利用C.B-17严重联合免疫缺陷(SCID)小鼠来研究这些小鼠肠道上皮内细胞的再填充情况。我们发现,注入SCID小鼠体内的肠道上皮内淋巴细胞(IEL)优先再填充肠道上皮。注射后约5周,我们可以在再填充的SCID小鼠中检测到大量的IEL。约70%的注射小鼠出现再填充,每只小鼠回收的细胞数量各不相同。回收的细胞来源于供体类型,并呈现典型的IEL表型。在IEL再填充的SCID小鼠的其他器官中有时能发现的供体类型T淋巴细胞数量通常较少。它们不能被针对IEL特异性标志物的抗体染色,其表型似乎更典型于通常在这些部位发现的T细胞。相比之下,使用包括胸腺细胞、派尔集合淋巴结淋巴细胞和骨髓细胞在内的其他器官的细胞,SCID小鼠的肠道上皮不能有效地被淋巴细胞再填充。根据我们的数据,我们得出结论,肠道IEL局限于肠道上皮,并且可能含有一种前体细胞类型,其优先再生自身群体的细胞。