In vivo imaging of specialized bone marrow endothelial microdomains for tumour engraftment
By D. Sipkins, Xunbin Wei, Juwell W. Wu, J. Runnels, D. Côté, T. Means, A. Luster, D. Scadden, Charles P Lin. Nature, 2005
909 citations recorded by the source corpus.
Subfields: Immunology and Allergy, Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/3442498bbb2a2dd5ae0a46a63213138e512b865c
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In Immunology and Allergy
In Molecular Biology
- Richard J. Gilbertson
- Vasilis Ntziachristos
- H. Kronenberg
- Erik Sahai
- Leonard I. Zon
- Stuart H. Orkin
- D. Scadden
- P. Dirks
In Oncology
Citations in the corpus
- The stem-cell niche as an entity of action (2006, background): “The sites on such vessels where primitive cells engage and diapedese seem to be highly discontinuous, and are functionally distinguished by abundant CXCL12 and E-selectin expressio”
- A perivascular niche for brain tumor stem cells. (2007, background): “, 2005), and that bone marrow endothelial niches are required for the homing and retention of normal hematopoietic and leukemic stem cells (Kiel et al., 2005; Sipkins et al., 2005).”
- Arteriolar niches maintain haematopoietic stem cell quiescence (2013, neutral): “…may represent a proliferative niche is consistent with recent studies indicating that E-selectin, an adhesion molecule constitutively expressed in certain BM sinusoid microdomains 43 , promotes HSC proliferation and blockade of E-selectin protects HSCs following chemotherapy or γ -irradiation 44 .”
- Endogenous Bone Marrow MSCs Are Dynamic, Fate-Restricted Participants in Bone Maintenance and Regeneration (2012, methodology): “Fourteen days after 4-OHT treatment, we scanned both sides of the sagittal (S.S.) and coronal (C.S.) sutures, which permitted examination of 40%–60% of the calvarial cavities of the mouse (Sipkins et al., 2005) (Figure 1B, left panel).”
- Engraftment and reconstitution of hematopoiesis is dependent on VEGFR2 mediated regeneration of sinusoidal endothelial cells (2009, neutral): “SECs have a unique expression of adhesion molecules, allowing the trafficking and homing of HSPCs to the BM (Kataoka and Tavassoli, 1985; Naiyer et al., 1999; Rafii et al., 1994, 1995; Sipkins et al., 2005; Kollet et al., 2006; Slayton et al., 2007).”
- Hematopoiesis: an evolving paradigm for stem cell biology. (2008, methodology): “As assessed by intravital microscopy, HSCs appear to reside in the periosteal region of calverium marrow (Sipkins et al., 2005).”
- Functional photoacoustic microscopy for high-resolution and noninvasive in vivo imaging (2006, neutral): “dtd" [ ]> Although optical absorption is strongly associated with the physiological status of biological tissue, existing high-resolution optical imaging modalities, including confocal microscop”
- BM mesenchymal stromal cell-derived exosomes facilitate multiple myeloma progression. (2013, neutral): “Using in vivo confocal imaging, we were able to visualize the BM vasculature and the possible presence of GFP + MM cells (38).”