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Establishment of a human T-cell line with deficient surface expression of glycosylphosphatidylinositol (GPI)-anchored proteins from a patient with paroxysmal nocturnal haemoglobinuria.

作者信息

Masuda T, Yonemura Y, Fujimoto K, Hidaka M, Nagakura S, Nakakuma H, Hata H, Sanada I, Kawakita M, Takatsuki K

机构信息

Second Department of Internal Medicine, Kumamoto University School of Medicine, Japan.

出版信息

Br J Haematol. 1994 May;87(1):24-30. doi: 10.1111/j.1365-2141.1994.tb04865.x.

DOI:10.1111/j.1365-2141.1994.tb04865.x
PMID:7524616
Abstract

A novel interleukin-2 dependent T-cell line, PMT-2Y, was established from the peripheral blood of a patient with paroxysmal nocturnal haemoglobinuria (PNH) by human T lymphotropic virus type I (HTLV-I)-mediated transformation. PMT-2Y cells are positive for CD2, CD3, CD4, CD25, T cell receptor alpha beta and HLA-DR, but negative for CD1, CD7, CD8, CD19 and CD20, indicating that the clone belongs to a helper/inducer subset of T cells. PMT-2Y cells have the monoclonal integration of HTLV-I proviral DNA, suggesting that they derived from a single clone. Moreover, they lack surface expression of complement regulatory proteins such as DAF (CD55) and CD59, that are the most important glycosylphosphatidylinositol (GPI)-anchored membrane proteins defective in haemopoietic cells of patients with PNH. Northern blot analysis, however, revealed the production of normal levels of DAF mRNAs. Thus, PMT-2Y is derived from a PNH T cell clone and may be a useful model to study PNH.

摘要

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