Literature DB >> 10605019

A role for pref-1 and HES-1 in thymocyte development.

M Kaneta1, M Osawa, K Sudo, H Nakauchi, A G Farr, Y Takahama.   

Abstract

T lymphocyte development requires a series of interactions between developing thymocytes and thymic epithelial (TE) cells. In this paper we show that TE cells in the developing thymus express Pref-1, a Delta-like cell-surface molecule. In fetal thymus organ cultures (FTOC), thymocyte cellularity was increased by the exogenous dimeric Pref-1 fusion protein, but was reduced by the soluble Pref-1 monomer or anti-Pref-1 Ab. Dimeric Pref-1 in FTOC also increased thymocyte expression of the HES-1 transcription factor. Thymocyte cellularity was increased in FTOC repopulated with immature thymocytes overexpressing HES-1, whereas FTOC from HES-1-deficient mice were hypocellular and unresponsive to the Pref-1 dimer. We detected no effects of either Pref-1 or HES-1 on developmental choice among thymocyte lineages. These results indicate that Pref-1 expressed by TE cells and HES-1 expressed by thymocytes are critically involved in supporting thymocyte cellularity.

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Year:  2000        PMID: 10605019     DOI: 10.4049/jimmunol.164.1.256

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  46 in total

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Journal:  EMBO J       Date:  2005-11-17       Impact factor: 11.598

6.  Mutational loss of PTEN induces resistance to NOTCH1 inhibition in T-cell leukemia.

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7.  Overexpression of Pref-1 in pancreatic islet β-cells in mice causes hyperinsulinemia with increased islet mass and insulin secretion.

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8.  Hes1 mediates the different responses of hematopoietic stem and progenitor cells to T cell leukemic environment.

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Review 10.  DLK1-DIO3 imprinted cluster in induced pluripotency: landscape in the mist.

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Journal:  Cell Mol Life Sci       Date:  2014-08-07       Impact factor: 9.261

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