Litcius/Paper detail

Neuroprotective Effect of Vascular Endothelial Growth Factor on Motoneurons of the Oculomotor System

Silvia Silva-Hucha, Ángel M. Pastor, Sara Morcuende

2021International Journal of Molecular Sciences31 citationsDOIOpen Access PDF

Abstract

Vascular endothelial growth factor (VEGF) was initially characterized as a potent angiogenic factor based on its activity on the vascular system. However, it is now well established that VEGF also plays a crucial role as a neuroprotective factor in the nervous system. A deficit of VEGF has been related to motoneuronal degeneration, such as that occurring in amyotrophic lateral sclerosis (ALS). Strikingly, motoneurons of the oculomotor system show lesser vulnerability to neurodegeneration in ALS compared to other motoneurons. These motoneurons presented higher amounts of VEGF and its receptor Flk-1 than other brainstem pools. That higher VEGF level could be due to an enhanced retrograde input from their target muscles, but it can also be produced by the motoneurons themselves and act in an autocrine way. By contrast, VEGF's paracrine supply from the vicinity cells, such as glial cells, seems to represent a minor source of VEGF for brainstem motoneurons. In addition, ocular motoneurons experiment an increase in VEGF and Flk-1 level in response to axotomy, not observed in facial or hypoglossal motoneurons. Therefore, in this review, we summarize the differences in VEGF availability that could contribute to the higher resistance of extraocular motoneurons to injury and neurodegenerative diseases.

Topics & Concepts

NeuroprotectionVascular endothelial growth factorNeuroscienceParacrine signallingNeurodegenerationBrainstemAutocrine signallingVascular endothelial growth factor ABiologyAxotomyMotor neuronVascular endothelial growth factor BAngiogenesisCentral nervous systemInternal medicineMedicineSpinal cordReceptorVEGF receptorsCancer researchDiseaseBiochemistryNerve injury and regenerationNeurogenesis and neuroplasticity mechanismsAxon Guidance and Neuronal Signaling