TY - JOUR
T1 - Spinal cord regeneration in Xenopus laevis
AU - Edwards-Faret, Gabriela
AU - Muñoz, Rosana
AU - Méndez-Olivos, Emilio E.
AU - Lee-Liu, Dasfne
AU - Tapia, Victor S.
AU - Larraín, Juan
N1 - Funding Information:
We thank members of our laboratory for their support, and especially our dedicated animal caretaker A. Farias. We thank H.T. Cline (The Scripps Research Institute) for our collaborative work with two-photon microscopy. This work was supported by funds from the CARE Chile UC-Centro de Envejecimiento y Regeneración (PFB 12/2007), MINREB (RC120003), FONDECYT (1141162), and ICGEB (CRP/CHI-13-01), FONDEF Idea (ID15I10349) to J.L. and Gastos Operacionales (21110043) to G.E.-F. G.E.-F., D.L.-L. and E.E.M.-O. are CONICYT PhD fellows.
PY - 2017/2/1
Y1 - 2017/2/1
N2 - Here we present a protocol for the husbandry of Xenopus laevis tadpoles and froglets, and procedures to study spinal cord regeneration. This includes methods to induce spinal cord injury (SCI); DNA and morpholino electroporation for genetic studies; in vivo imaging for cell analysis; a swimming test to measure functional recovery; and a convenient model for screening for new compounds that promote neural regeneration. These protocols establish X. laevis as a unique model organism for understanding spinal cord regeneration by comparing regenerative and nonregenerative stages. This protocol can be used to understand the molecular and cellular mechanisms involved in nervous system regeneration, including neural stem and progenitor cell (NSPC) proliferation and neurogenesis, extrinsic and intrinsic mechanisms involved in axon regeneration, glial response and scar formation, and trophic factors. For experienced personnel, husbandry takes 1-2 months; SCI can be achieved in 5-15 min; and swimming recovery takes 20-30 d.
AB - Here we present a protocol for the husbandry of Xenopus laevis tadpoles and froglets, and procedures to study spinal cord regeneration. This includes methods to induce spinal cord injury (SCI); DNA and morpholino electroporation for genetic studies; in vivo imaging for cell analysis; a swimming test to measure functional recovery; and a convenient model for screening for new compounds that promote neural regeneration. These protocols establish X. laevis as a unique model organism for understanding spinal cord regeneration by comparing regenerative and nonregenerative stages. This protocol can be used to understand the molecular and cellular mechanisms involved in nervous system regeneration, including neural stem and progenitor cell (NSPC) proliferation and neurogenesis, extrinsic and intrinsic mechanisms involved in axon regeneration, glial response and scar formation, and trophic factors. For experienced personnel, husbandry takes 1-2 months; SCI can be achieved in 5-15 min; and swimming recovery takes 20-30 d.
UR - http://www.scopus.com/inward/record.url?scp=85010951365&partnerID=8YFLogxK
U2 - 10.1038/nprot.2016.177
DO - 10.1038/nprot.2016.177
M3 - Article
C2 - 28102835
AN - SCOPUS:85010951365
SN - 1754-2189
VL - 12
SP - 372
EP - 389
JO - Nature Protocols
JF - Nature Protocols
IS - 2
ER -