FES-Cre targets phosphatidylinositol glycan class A (PIGA) inactivation to hematopoietic stem cells in the bone marrow Journal Article


Authors: Keller, P.; Payne, J. L.; Tremml, G.; Greer, P. A.; Gaboli, M.; Pandolfi, P. P.; Bessler, M.
Article Title: FES-Cre targets phosphatidylinositol glycan class A (PIGA) inactivation to hematopoietic stem cells in the bone marrow
Abstract: A somatic mutation in the X-linked phosphatidylinositol glycan class A (PIGA) gene causes the loss of glycosyl phosphatidylinositol (GPI)-linked proteins on blood cells from patients with paroxysmal nocturnal hemoglobinuria. Because all blood cell lineages may be affected it is thought that the mutation occurs in a hematopoietic stein cell. In transgenic mice, germline transmission of an inactive Papa gene is embryonic lethal. To inactivate the murine Piga gene in early hematopoiesis we therefore chose conditional gene inactivation using the Cre/loxP system. We expressed Cre recombinase under the transcription regulatory sequences of the Human c-fes gene. FES-Cre inactivated PIGA in hematopoietic cells of puce carrying a floxed Piga allele (LF mice). PIGA(-) cells were found in all hematopoietic lineages of definitive but not primitive hematopoiesis. Their proportions were low in newborn mice but subsequently increased continuously to produce for the first time mice that have almost exclusively PIGA(-) blood cells. The loss of GPI-linked proteins occurred mainly in c-kit(+)CD34(+)Lin(-) progenitor cells before the CFU-GEMM stage. Using bone marrow reconstitution experiments with purified PIGA- cells we demonstrate that LF mice have long-term bone marrow repopulating cells that lack GPI-linked proteins, indicating that recombination of the floxed Piga allele occurs in the hematopoietic stein cell.
Keywords: protein; stem cell; hematopoiesis; transgenic mice; differentiation; paroxysmal nocturnal hemoglobinuria; expression; membrane; paroxysmal-nocturnal hemoglobinuria; kinase-activity; protooncogene; pu.1; c-fes; conditional gene inactivation; a gene; fps/fes
Journal Title: Journal of Experimental Medicine
Volume: 194
Issue: 5
ISSN: 0022-1007
Publisher: Rockefeller University Press  
Date Published: 2001-09-03
Start Page: 581
End Page: 589
Language: English
ACCESSION: WOS:000170873700006
DOI: 10.1084/jem.194.5.581
PROVIDER: wos
PMCID: PMC2195941
PUBMED: 11535627
Notes: Article -- Source: Wos
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  1. Mirella P Gaboli
    19 Gaboli
  2. Gabriele   Tremml
    15 Tremml