TY - JOUR
T1 - Identification of axon growth promoters in the secretome of the deer antler velvet
AU - Pita-Thomas, Wolfgang
AU - Barroso-García, Gemma
AU - Moral, Veronica
AU - Hackett, Amber R.
AU - Cavalli, Valeria
AU - Nieto-Diaz, Manuel
N1 - Funding Information:
This work was supported by the Consejeria de Sanidad de Castilla la Mancha (Grant PI2008-38 ). We thank for their technical and logistic support to the Fundacion del Hospital Nacional de Paraplejicos para la Investigacion y la Integracion (FUHNPAIIN) and the microscopy and proteomics facilities of the Experimental Neurology Unit, Hospital Nacional de Paraplejicos, Toledo (Spain).
Publisher Copyright:
© 2016 IBRO
PY - 2017/1/6
Y1 - 2017/1/6
N2 - Every spring, deer cast their old antlers and initiate a regeneration process, which yields a new set of antlers of up to 1 m in length. Over the course of three months, branches of the trigeminal nerve, originating from the frontal skull, innervate velvet, a modified skin that covers the regenerating antler. The rate of growth of these axons reaches up to 2 cm per day making them the fastest regenerating axons in adult mammals. Here, we aim to identify the factors secreted by velvet that promote such high speed axon growth. Our experiments with cultures of adult rat trigeminal neurons demonstrate that conditioned medium harvested from velvet organotypic cultures has greater axon growth-promoting properties than a medium conditioned by normal skin. The axon growth-promoting effects of velvet act synergistically with the extracellular matrix (ECM) protein laminin, a component of the basal lamina present in the deer antler. Our proteomic analyses identified several axon growth promoters in the velvet-conditioned medium (VCM), including soluble proteins such as nerve growth factor (NGF) and apolipoprotein A-1, as well as matrix extracellular proteins, such as periostin and SPARC. Additional in vitro analyses allowed us to determine that a synergic relationship between periostin and NGF may contribute to neurite growth-promoting effects of velvet secretome. A combinatorial approach using these factors may promote regeneration at high speeds in patients with peripheral neuropathies.
AB - Every spring, deer cast their old antlers and initiate a regeneration process, which yields a new set of antlers of up to 1 m in length. Over the course of three months, branches of the trigeminal nerve, originating from the frontal skull, innervate velvet, a modified skin that covers the regenerating antler. The rate of growth of these axons reaches up to 2 cm per day making them the fastest regenerating axons in adult mammals. Here, we aim to identify the factors secreted by velvet that promote such high speed axon growth. Our experiments with cultures of adult rat trigeminal neurons demonstrate that conditioned medium harvested from velvet organotypic cultures has greater axon growth-promoting properties than a medium conditioned by normal skin. The axon growth-promoting effects of velvet act synergistically with the extracellular matrix (ECM) protein laminin, a component of the basal lamina present in the deer antler. Our proteomic analyses identified several axon growth promoters in the velvet-conditioned medium (VCM), including soluble proteins such as nerve growth factor (NGF) and apolipoprotein A-1, as well as matrix extracellular proteins, such as periostin and SPARC. Additional in vitro analyses allowed us to determine that a synergic relationship between periostin and NGF may contribute to neurite growth-promoting effects of velvet secretome. A combinatorial approach using these factors may promote regeneration at high speeds in patients with peripheral neuropathies.
KW - axon regeneration
KW - deer antler
KW - peripheral nervous system
KW - proteomics
KW - secreted proteins
UR - http://www.scopus.com/inward/record.url?scp=84995972547&partnerID=8YFLogxK
U2 - 10.1016/j.neuroscience.2016.10.063
DO - 10.1016/j.neuroscience.2016.10.063
M3 - Article
C2 - 27818162
AN - SCOPUS:84995972547
SN - 0306-4522
VL - 340
SP - 333
EP - 344
JO - Neuroscience
JF - Neuroscience
ER -