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Review
. 2014 Jul 9:6:14.
doi: 10.1186/2045-824X-6-14. eCollection 2014.

Flow-regulated lymphatic vasculature development and signaling

Affiliations
Review

Flow-regulated lymphatic vasculature development and signaling

Yingdi Wang et al. Vasc Cell. .

Abstract

The role of blood flow in regulating signaling pathways and gene expression in the blood vasculature is well known. Recent studies have identified equally important roles of flow-mediated signaling in the lymphatic circulation including control of lymphatic vascular growth, remodeling, regeneration and maintenance of the lymphatic fate. In this review, we summarize these advances focusing on the role of fluid dynamics in control of lymphatic vasculature formation.

Keywords: Flow; Lymphatic endothelial cells; Lymphatic vascular development; Shear stress; Signaling.

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Figures

Figure 1
Figure 1
Fluid flow in lymphatic vasculature development in mice. (A) Flow triggers lymphatic valve development. At approximately embryonic day (E)16.0, lymph flow induces Cx37 expression and activates calcineurin/NFATc1 signaling in lymphatic-valve-forming cells initiating luminal valve development. (B) Fluid flow plays a role in lymphatic fate maintenance. In mice, loss of Slp-76 results in shunt formation between blood and lymphatic vessels in mesentery and, therefore mixing of blood and lymphatic circulation. The presence of blood flow in lymphatic vessels in Slp-76 null mice causes the change of lymphatic fate to a venous identity.

References

    1. Brown JD, DiChiara MR, Anderson KR, Gimbrone MA, Topper JN. MEKK-1, a component of the stress (stress-activated protein kinase/c-Jun N-terminal kinase) pathway, can selectively activate Smad2-mediated transcriptional activation in endothelial cells. J Biol Chem. 1999;274:8797–8805. - PubMed
    1. Chien S, Li S, Shyy JY. Effects of mechanical forces on signal transduction and gene expression in endothelial cells. Hypertension. 1998;31:162–169. - PubMed
    1. Topper JN, Gimbrone MA Jr. Blood flow and vascular gene expression: fluid shear stress as a modulator of endothelial phenotype. Mol Med Today. 1999;5:40–46. - PubMed
    1. Wasserman SM, Topper JN. Adaptation of the endothelium to fluid flow: in vitro analyses of gene expression and in vivo implications. Vasc Med. 2004;9:35–45. - PubMed
    1. Chiu J-J, Usami S, Chien S. Vascular endothelial responses to altered shear stress: pathologic implications for atherosclerosis. Ann Med. 2009;41:19–28. - PubMed

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