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Quantitative Proteomics After Spinal Cord Injury (SCI) in a Regenerative and a Nonregenerative Stage in the Frog Xenopus laevis.
Lee-Liu, Dasfne; Sun, Liangliang; Dovichi, Norman J; Larraín, Juan.
Affiliation
  • Lee-Liu D; From the ‡Center for Aging and Regeneration, Millennium Nucleus in Regenerative Biology, Faculty of Biological Sciences, P. Universidad Católica de Chile, Alameda 340, Santiago, Chile.
  • Sun L; §Department of Chemistry, Michigan State University, East Lansing, Michigan 48824.
  • Dovichi NJ; ¶Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556.
  • Larraín J; From the ‡Center for Aging and Regeneration, Millennium Nucleus in Regenerative Biology, Faculty of Biological Sciences, P. Universidad Católica de Chile, Alameda 340, Santiago, Chile ; jlarrain@bio.puc.cl.
Mol Cell Proteomics ; 17(4): 592-606, 2018 04.
Article in En | MEDLINE | ID: mdl-29358338
The capacity to regenerate the spinal cord after an injury is a coveted trait that only a limited group of nonmammalian organisms can achieve. In Xenopus laevis, this capacity is only present during larval or tadpole stages, but is absent during postmetamorphic frog stages. This provides an excellent model for comparative studies between a regenerative and a nonregenerative stage to identify the cellular and molecular mechanisms that explain this difference in regenerative potential. Here, we used iTRAQ chemistry to obtain a quantitative proteome of the spinal cord 1 day after a transection injury in regenerative and nonregenerative stage animals, and used sham operated animals as controls. We quantified a total of 6,384 proteins, with 172 showing significant differential expression in the regenerative stage and 240 in the nonregenerative stage, with an overlap of only 14 proteins. Functional enrichment analysis revealed that although the regenerative stage downregulated synapse/vesicle and mitochondrial proteins, the nonregenerative stage upregulated lipid metabolism proteins, and downregulated ribosomal and translation control proteins. Furthermore, STRING network analysis showed that proteins belonging to these groups are highly interconnected, providing interesting candidates for future functional studies. Data are available via ProteomeXchange with identifier PXD006993.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Regeneration / Spinal Cord / Spinal Cord Injuries / Xenopus laevis / Amphibian Proteins Limits: Animals Language: En Journal: Mol Cell Proteomics Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA Year: 2018 Document type: Article Affiliation country: Chile Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Regeneration / Spinal Cord / Spinal Cord Injuries / Xenopus laevis / Amphibian Proteins Limits: Animals Language: En Journal: Mol Cell Proteomics Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA Year: 2018 Document type: Article Affiliation country: Chile Country of publication: United States