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Cited by 405

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Angiocrine factors from Akt-activated endothelial cells balance self-renewal and differentiation of haematopoietic stem cells

Open access
Kobayashi, Hideki, Butler, Jason M., O'Donnell, Rebekah, Kobayashi, Mariko, Ding, Bi-Sen, Bonner, Bryant, Chiu, Vi K., Nolan, Daniel J., Shido, Koji, Benjamin, Laura, Rafii, Shahin·2010·Nature Cell Biology

Abstract

Endothelial cells establish an instructive vascular niche that reconstitutes haematopoietic stem and progenitor cells (HSPCs) through release of specific paracrine growth factors, known as angiocrine factors. However, the mechanism by which endothelial cells balance the rate of proliferation and lineage-specific differentiation of HSPCs is unknown. Here, we demonstrate that Akt activation in endothelial cells, through recruitment of mTOR, but not the FoxO pathway, upregulates specific angiocrine factors that support expansion of CD34−Flt3− KLS HSPCs with long-term haematopoietic stem cell (LT-HSC) repopulation capacity. Conversely, co-activation of Akt-stimulated endothelial cells with p42/44 MAPK shifts the balance towards maintenance and differentiation of the HSPCs. Selective activation of Akt1 in the endothelial cells of adult mice increased the number of colony forming units in the spleen and CD34−Flt3− KLS HSPCs with LT-HSC activity in the bone marrow, accelerating haematopoietic recovery. Therefore, the activation state of endothelial cells modulates reconstitution of HSPCs through the modulation of angiocrine factors, with Akt–mTOR-activated endothelial cells supporting the self-renewal of LT-HSCs and expansion of HSPCs, whereas MAPK co-activation favours maintenance and lineage-specific differentiation of HSPCs.

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Crossref · 10.1038/ncb2108

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Metadata

Authors
Kobayashi, H., Butler, J. M., O'Donnell, R., Kobayashi, M., Ding, B.-S., Bonner, B., Chiu, V. K., Nolan, D. J., Shido, K., Benjamin, L., & Rafii, S.
Venue
Nature Cell Biology
Published
2010-10-24
Volume
12
Issue
11
Pages
1046-1056
ISSN
  • 1465-7392 (ISSN-L)
  • 1476-4679
OpenAlex
W2124977778
Cited by
405
References
3
FWCI
19.57
Type
journal article
Language
en
Open access
green

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