Functional ramifications for the loss of P-selectin expression on hematopoietic and leukemic stem cells.
Hematopoiesis is a tightly regulated biological process that relies upon complicated interactions between blood cells and their microenvironment to preserve the homeostatic balance of long-term hematopoietic stem cells (LT-HSCs), short-term HSCs (ST-HSCs), multipotent progenitors (MPPs), and differe...
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Public Library of Science (PLoS)
2011-01-01
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Online Access: | http://europepmc.org/articles/PMC3200313?pdf=render |
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author | Con Sullivan Yaoyu Chen Yi Shan Yiguo Hu Cong Peng Haojian Zhang Linghong Kong Shaoguang Li |
author_facet | Con Sullivan Yaoyu Chen Yi Shan Yiguo Hu Cong Peng Haojian Zhang Linghong Kong Shaoguang Li |
author_sort | Con Sullivan |
collection | DOAJ |
description | Hematopoiesis is a tightly regulated biological process that relies upon complicated interactions between blood cells and their microenvironment to preserve the homeostatic balance of long-term hematopoietic stem cells (LT-HSCs), short-term HSCs (ST-HSCs), multipotent progenitors (MPPs), and differentiated cells. Adhesion molecules like P-selectin (encoded by the Selp gene) are essential to hematopoiesis, and their dysregulation has been linked to leukemogenesis. Like HSCs, leukemic stem cells (LSCs) depend upon their microenvironments for survival and propagation. P-selectin plays a crucial role in Philadelphia chromosome-positive (Ph(+)) chronic myeloid leukemia (CML). In this paper, we show that cells deficient in P-selectin expression can repopulate the marrow more efficiently than wild type controls. This results from an increase in HSC self-renewal rather than alternative possibilities like increased homing velocity or cell cycle defects. We also show that P-selectin expression on LT-HSCs, but not ST-HSCs and MPPs, increases with aging. In the absence of P-selectin expression, mice at 6 months of age possess increased levels of short-term HSCs and multipotent progenitors. By 11 months of age, there is a shift towards increased levels of long-term HSCs. Recipients of BCR-ABL-transduced bone marrow cells from P-selectin-deficient donors develop a more aggressive CML, with increased percentages of LSCs and progenitors. Taken together, our data reveal that P-selectin expression on HSCs and LSCs has important functional ramifications for both hematopoiesis and leukemogenesis, which is most likely attributable to an intrinsic effect on stem cell self-renewal. |
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language | English |
last_indexed | 2024-12-22T10:22:40Z |
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spelling | doaj.art-915a74db923241078e55a718f5fb3b132022-12-21T18:29:35ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01610e2624610.1371/journal.pone.0026246Functional ramifications for the loss of P-selectin expression on hematopoietic and leukemic stem cells.Con SullivanYaoyu ChenYi ShanYiguo HuCong PengHaojian ZhangLinghong KongShaoguang LiHematopoiesis is a tightly regulated biological process that relies upon complicated interactions between blood cells and their microenvironment to preserve the homeostatic balance of long-term hematopoietic stem cells (LT-HSCs), short-term HSCs (ST-HSCs), multipotent progenitors (MPPs), and differentiated cells. Adhesion molecules like P-selectin (encoded by the Selp gene) are essential to hematopoiesis, and their dysregulation has been linked to leukemogenesis. Like HSCs, leukemic stem cells (LSCs) depend upon their microenvironments for survival and propagation. P-selectin plays a crucial role in Philadelphia chromosome-positive (Ph(+)) chronic myeloid leukemia (CML). In this paper, we show that cells deficient in P-selectin expression can repopulate the marrow more efficiently than wild type controls. This results from an increase in HSC self-renewal rather than alternative possibilities like increased homing velocity or cell cycle defects. We also show that P-selectin expression on LT-HSCs, but not ST-HSCs and MPPs, increases with aging. In the absence of P-selectin expression, mice at 6 months of age possess increased levels of short-term HSCs and multipotent progenitors. By 11 months of age, there is a shift towards increased levels of long-term HSCs. Recipients of BCR-ABL-transduced bone marrow cells from P-selectin-deficient donors develop a more aggressive CML, with increased percentages of LSCs and progenitors. Taken together, our data reveal that P-selectin expression on HSCs and LSCs has important functional ramifications for both hematopoiesis and leukemogenesis, which is most likely attributable to an intrinsic effect on stem cell self-renewal.http://europepmc.org/articles/PMC3200313?pdf=render |
spellingShingle | Con Sullivan Yaoyu Chen Yi Shan Yiguo Hu Cong Peng Haojian Zhang Linghong Kong Shaoguang Li Functional ramifications for the loss of P-selectin expression on hematopoietic and leukemic stem cells. PLoS ONE |
title | Functional ramifications for the loss of P-selectin expression on hematopoietic and leukemic stem cells. |
title_full | Functional ramifications for the loss of P-selectin expression on hematopoietic and leukemic stem cells. |
title_fullStr | Functional ramifications for the loss of P-selectin expression on hematopoietic and leukemic stem cells. |
title_full_unstemmed | Functional ramifications for the loss of P-selectin expression on hematopoietic and leukemic stem cells. |
title_short | Functional ramifications for the loss of P-selectin expression on hematopoietic and leukemic stem cells. |
title_sort | functional ramifications for the loss of p selectin expression on hematopoietic and leukemic stem cells |
url | http://europepmc.org/articles/PMC3200313?pdf=render |
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