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An evolutionarily conserved role for VEGF signaling in the expansion of non-vascular tissue during regeneration.

Savage, A. M.; Wagner, A. C.; Kim, R. T.; Gilbert, P.; Singer, H. D.; Chen, E.; Kim, E. M.; Lopez, N.; Dooling, K. E.; Paoli, J. C.; Wu, S. Y. C.; Bohm, S.; Chilambi, R.; Froitzheim, T.; Blair, S. J.; Powell, C. J.; Abouelela, A.; Luong, A. G.; Thornton, K. N.; Tajer, B.; Payzin-Dogru, D.; Whited, J. L.

2024-10-03 developmental biology
10.1101/2024.10.01.616057 bioRxiv
Show abstract

Salamanders are capable of regenerating whole limbs throughout life, a feat that is unmatched within tetrapods. Limb regeneration is dependent upon the formation of a blastema, which contains undifferentiated cells capable of giving rise to most cells of the regenerated limb. Innervation is required for regeneration, along with many signaling pathways, including FGF, BMP and Wnt, but the role of VEGF signaling during salamander limb regeneration is not well understood. Here we show that VEGF signaling is essential for limb regeneration and that blastema cells and limb fibroblasts display impaired proliferation in the absence of VEGF signaling. By performing analogous experiments in planaria, which lack vasculature, we show a potential evolutionarily conserved role for VEGF in the expansion of blastema tissues that is separable from angiogenesis. Moreover, loss of VEGF signaling reduces induction of EMT-like processes, suggesting VEGF signaling functions upstream of the expression of EMT transcription factors, including Snai2. These findings highlight potential roles for VEGF signaling during regeneration which may extend beyond typical findings related to angiogenesis.

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