Literature DB >> 10901596

Organ specificity of c-kit+ lymphoid precursors in the liver, thymus, and bone marrow.

T Shimizu1, M Bannai, H Kawamura, S Yamamoto, H Oya, S Maruyama, M Minagawa, T Kawamura, H Watanabe, K Hatakeyama, T Abo.   

Abstract

c-kit+Lin- cells are present in various immune organs, including the liver, thymus, and bone marrow, where lymphoid, myeloid, or erythroid cells are generated. To compare their properties as lymphoid precursors, c-kit+Lin- cells purified from various organs of B6.Ly5.1 mice were injected into 6.5 Gy-irradiated B6.Ly5.2 mice. Depending on the source of the c-kit cells, the degree of entrance and expansion of lymphoid cells differed in the liver and thymus of recipient mice. c-kit+ cells isolated from the bone marrow entered and expanded prominently in both the liver and thymus, whereas c-kit+ cells from the thymus did not do so at all. On the other hand, c-kit+ cells isolated from the liver and spleen showed an intermediate pattern, namely, they took a long time to enter and expand in the liver and thymus of recipient mice. All of these c-kit+ cells had the potential to give rise to lymphoid cells, which were specific to the liver and thymus, respectively. We previously showed that progenitor cells for extrathymic T cells in the liver and those for conventional T cells in the thymus are not always supplied by the bone marrow, as shown by experiments using parabiosis. Taken together with those previous data, the present results suggest that c-kit+Lin- cells isolated from various immune organs have organ specific properties.

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Year:  2000        PMID: 10901596     DOI: 10.1034/j.1600-0609.2000.90158.x

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


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Journal:  Stem Cells Transl Med       Date:  2020-03-03       Impact factor: 6.940

3.  Fibrotic liver microenvironment promotes Dll4 and SDF-1-dependent T-cell lineage development.

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  3 in total

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