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Phosphatidylinositol 3‐kinases are involved in the all‐ trans retinoic acid‐induced upregulation of CD38 antigen on human haematopoietic cells
Author(s) -
Lewandowski Daniel,
Linassier Claude,
Iochmann Sophie,
Degenne Michel,
Domenech Jorge,
Colombat Philippe,
Binet Christian,
Hérault Olivier
Publication year - 2002
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1046/j.1365-2141.2002.03601.x
Subject(s) - cd38 , haematopoiesis , retinoic acid , antigen , downregulation and upregulation , acute promyelocytic leukemia , myeloid , biology , cd34 , ly294002 , tretinoin , microbiology and biotechnology , cancer research , stem cell , chemistry , immunology , phosphatidylinositol , kinase , cell culture , biochemistry , genetics , gene
Summary. All‐ trans retinoic acid (ATRA) is a specific inducer of CD38 antigen on marrow CD34 + cells as well as on blast cells in acute promyelocytic and myeloblastic leukaemia. The CD38 antigen contributes to the control of blast cell proliferation, and the upregulation of CD38 might constitute an element in the pathogenesis of retinoic acid syndrome. The aim of this study was to determine whether phosphoinositide 3‐kinase (PI3‐K) is involved in the modification of CD38 antigen expression on myeloid cells, as PI3‐K plays a major role in the ATRA‐induced granulocytic differentiation of HL‐60 cells. We evaluated the effects of PI3‐K inhibitors (wortmannin and LY294002) on the levels of CD38 antigen and mRNA in HL‐60 and normal marrow CD34 + cells exposed to ATRA (1 µmol/l). The inhibitors prevented increase in CD38 mRNA expression and the overexpression of membrane CD38 antigen, without modification of the cytoplasmic level of this antigen. Interestingly, PI3‐K activity was also necessary for CD38 expression on normal marrow CD34 + cells and for the ATRA‐induced upregulation of CD157, a CD38‐related antigen. In conclusion, PI3‐K activity plays an essential role in the regulation of CD38 expression on human haematopoietic cells, and might constitute an interesting therapeutic target in haematological disorders involving CD38 overexpression.