2001
DOI: 10.1016/s0301-472x(01)00676-2
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Notch receptors and hematopoiesis

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Cited by 117 publications
(88 citation statements)
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References 150 publications
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“…In addition, a higher proportion of total immature memory CD8 + and CD4 + T cells are associated with improved prognosis in chronic HIV-1 infection (54) and can be enriched in the absence of viremia and immune activation in treated HIV-1-positive individuals (55). Interestingly, we found evidence that Notch signaling, previously mostly shown to regulate hematopoietic and thymic precursor cell differentiation (37,38), is also involved in regulating the transition of long-lasting PD-1 lo into short-lived PD-1 hi Tfh-like cells. This suggest that stem cell pathways, previously recognized in the context of traditional organ-specific stem cells, may also contribute to regulation and fate decisions within the memory Tfh pools, and may offer molecular targets for selectively influencing memory Tfh development.…”
Section: Cxcr3mentioning
confidence: 70%
See 1 more Smart Citation
“…In addition, a higher proportion of total immature memory CD8 + and CD4 + T cells are associated with improved prognosis in chronic HIV-1 infection (54) and can be enriched in the absence of viremia and immune activation in treated HIV-1-positive individuals (55). Interestingly, we found evidence that Notch signaling, previously mostly shown to regulate hematopoietic and thymic precursor cell differentiation (37,38), is also involved in regulating the transition of long-lasting PD-1 lo into short-lived PD-1 hi Tfh-like cells. This suggest that stem cell pathways, previously recognized in the context of traditional organ-specific stem cells, may also contribute to regulation and fate decisions within the memory Tfh pools, and may offer molecular targets for selectively influencing memory Tfh development.…”
Section: Cxcr3mentioning
confidence: 70%
“…To investigate mechanisms that may dictate the ability of PD-1 lo pTfh cells to repopulate PD-1 hi pTfh cells, we focused on the Notch signaling cascade, which has previously been implicated in regulating the developmental fate of organ-specific stem cells (37,38), memory T cells (39)(40)(41), and T follicular helper cells (42). We observed that Notch receptors 2 and 4, as well as the Notch active intracellular domain, were upregulated on CXCR5 + T cells after 6 days of coculture with autologous B cells and SEB in the presence of GSI compared with DMSO (n = 6).…”
Section: Cd95mentioning
confidence: 99%
“…A number of in vivo and in vitro studies have demonstrated the roles of the Notch signaling pathway in stem cells, early progenitor cells and in the development of cancers. The involvement of Notch signaling in cancer was first identified in T-cell acute lymphoblastic leukemia (T-ALL) where chromosomal translocation (7;9) leads to the constitutive activation of Notch signaling (23)(24)(25)(26) that was further demonstrated in a mouse model where expression of a constitutively active Notch1 protein led to the development of T-cell lymphoma (27,28).…”
Section: Signaling Pathways In Cancer Stem Cellsmentioning
confidence: 99%
“…Notch signaling pathway plays an important role in myelosuppression restoration and is capable of adjusting various stages of hematopoietic cells [6][7]. Notch receptors and ligands are highly expressed in hematopoietic progenitor cells and marrow stromal cells [8].…”
Section: Introductionmentioning
confidence: 99%