Cardiovascular actions of neurotrophins

Andrea Caporali, Costanza Emanueli

Research output: Contribution to journalArticlepeer-review


Neurotrophins were christened in consideration of their actions on the nervous system and, for a long time, they were the exclusive interest of neuroscientists. However, more recently, this family of proteins has been shown to possess essential cardiovascular functions. During cardiovascular development, neurotrophins and their receptors are essential factors in the formation of the heart and critical regulator of vascular development. Postnatally, neurotrophins control the survival of endothelial cells, vascular smooth muscle cells, and cardiomyocytes and regulate angiogenesis and vasculogenesis, by autocrine and paracrine mechanisms. Recent studies suggest the capacity of neurotrophins, via their tropomyosin-kinase receptors, to promote therapeutic neovascularization in animal models of hindlimb ischemia. Conversely, the neurotrophin low-affinity p75(NTR) receptor induces apoptosis of endothelial cells and vascular smooth muscle cells and impairs angiogenesis. Finally, nerve growth factor looks particularly promising in treating microvascular complications of diabetes or reducing cardiomyocyte apoptosis in the infarcted heart. These seminal discoveries have fuelled basic and translational research and thus opened a new field of investigation in cardiovascular medicine and therapeutics. Here, we review recent progress on the molecular signaling and roles played by neurotrophins in cardiovascular development, function, and pathology, and we discuss therapeutic potential of strategies based on neurotrophin manipulation.
Original languageEnglish
Pages (from-to)279-308
Number of pages30
JournalPhysiological reviews
Issue number1
Publication statusPublished - Jan 2009


  • Animals
  • Cardiovascular Physiological Phenomena
  • Cardiovascular System
  • Humans
  • Neovascularization, Pathologic
  • Neovascularization, Physiologic
  • Nerve Growth Factors
  • Receptor, Nerve Growth Factor
  • Receptor, trkA


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