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ATP-Binding Cassette Transporters and HDL Suppress Hematopoietic Stem Cell Proliferation
Author(s) -
Laurent YvanCharvet,
Tamara A. Pagler,
Emmanuel L. Gautier,
Serine Avagyan,
Read Siry,
Seongah Han,
Carrie L. Welch,
Nan Wang,
Gwendalyn J. Randolph,
Hans Snoeck,
Alan R. Tall
Publication year - 2010
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1189731
Subject(s) - atp binding cassette transporter , stem cell , haematopoiesis , hematopoietic stem cell , microbiology and biotechnology , transporter , cell growth , chemistry , biology , biochemistry , gene
Elevated leukocyte cell numbers (leukocytosis), and monocytes in particular, promote atherosclerosis; however, how they become increased is poorly understood. Mice deficient in the adenosine triphosphate-binding cassette (ABC) transporters ABCA1 and ABCG1, which promote cholesterol efflux from macrophages and suppress atherosclerosis in hypercholesterolemic mice, displayed leukocytosis, a transplantable myeloproliferative disorder, and a dramatic expansion of the stem and progenitor cell population containing Lin(-)Sca-1(+)Kit+ (LSK) in the bone marrow. Transplantation of Abca1(-/-) Abcg1(-/-) bone marrow into apolipoprotein A-1 transgenic mice with elevated levels of high-density lipoprotein (HDL) suppressed the LSK population, reduced leukocytosis, reversed the myeloproliferative disorder, and accelerated atherosclerosis. The findings indicate that ABCA1, ABCG1, and HDL inhibit the proliferation of hematopoietic stem and multipotential progenitor cells and connect expansion of these populations with leukocytosis and accelerated atherosclerosis.

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