AI Article Synopsis

  • Controlling angiogenesis is essential for various biological processes, and while growth factors and cytokines are known regulators, their complete mechanisms are still not fully understood.
  • Recent studies reveal that electrical stimulation can significantly enhance angiogenesis by increasing the production of vascular endothelial growth factor (VEGF) in muscle cells, indicating a link between electrical fields and blood vessel formation.
  • Applied electric fields of low magnitude can directly stimulate VEGF production and influence endothelial cell behaviors like migration and reorientation through specific signaling pathways, suggesting potential therapeutic applications for guiding angiogenesis.

Article Abstract

Controlling angiogenesis is crucial. Growth factors and cytokines are key regulators but a full understanding remains elusive. Endogenous electrical potential differences exist within and around the vasculature, both in relation to blood flow and in situations where active angiogenesis occurs, such as wound healing, development and tumor growth. Recent work shows that electrical stimulation induces significant angiogenesis in vivo, through enhanced vascular endothelial growth factor (VEGF) production by muscle cells. We report that applied electric fields (EFs) of small physiological magnitude directly stimulate VEGF production by endothelial cells in culture without the presence of any other cell type. EFs as low as 75-100 mV mm-1 (1.5-2.0 mV across an endothelial cell) directed the reorientation, elongation and migration of endothelial cells in culture. These pre-angiogenic responses required VEGF receptor activation and were mediated through PI3K-Akt and Rho-ROCK signaling pathways, resulting in reorganization of the actin cytoskeleton. This indicates that endogenous EFs might play a role in angiogenesis in vivo by stimulating the VEGF receptor signaling pathway, to induce key pre-angiogenic responses. In addition, it raises the feasibility of using applied EFs to initiate and guide angiogenesis through direct effects on endothelial cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1459284PMC
http://dx.doi.org/10.1242/jcs.00868DOI Listing

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