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Highly conserved molecular pathways, including Wnt signaling, promote functional recovery from spinal cord injury in lampreys

  • Paige E. Herman
  • , Angelos Papatheodorou
  • , Stephanie A. Bryant
  • , Courtney K.M. Waterbury
  • , Joseph R. Herdy
  • , Anthony A. Arcese
  • , Joseph D. Buxbaum
  • , Jeramiah J. Smith
  • , Jennifer R. Morgan
  • , Ona Bloom

Producción científica: Articlerevisión exhaustiva

60 Citas (Scopus)

Resumen

In mammals, spinal cord injury (SCI) leads to dramatic losses in neurons and synaptic connections, and consequently function. Unlike mammals, lampreys are vertebrates that undergo spontaneous regeneration and achieve functional recovery after SCI. Therefore our goal was to determine the complete transcriptional responses that occur after SCI in lampreys and to identify deeply conserved pathways that promote regeneration. We performed RNA-Seq on lamprey spinal cord and brain throughout the course of functional recovery. We describe complex transcriptional responses in the injured spinal cord, and somewhat surprisingly, also in the brain. Transcriptional responses to SCI in lampreys included transcription factor networks that promote peripheral nerve regeneration in mammals such as Atf3 and Jun. Furthermore, a number of highly conserved axon guidance, extracellular matrix, and proliferation genes were also differentially expressed after SCI in lampreys. Strikingly, ~3% of differentially expressed transcripts belonged to the Wnt pathways. These included members of the Wnt and Frizzled gene families, and genes involved in downstream signaling. Pharmacological inhibition of Wnt signaling inhibited functional recovery, confirming a critical role for this pathway. These data indicate that molecular signals present in mammals are also involved in regeneration in lampreys, supporting translational relevance of the model.

Idioma originalEnglish
Número de artículo742
PublicaciónScientific Reports
Volumen8
N.º1
DOI
EstadoPublished - dic 1 2018

Nota bibliográfica

Publisher Copyright:
© 2018 The Author(s).

Financiación

We wish to thank AML Labs, Clara Wilson, Ismael Rodriquez, Dylan Lukes, and Nataliya Timoshevskaya for technical support. We wish to thank Joel Smith, Avis Cohen (Univ. Maryland), and S. Randal Voss (Univ. Kentucky) for early discussions, Betty Diamond and K.J. Tracey (Feinstein), E.T. Walters (UT Houston) and Phil Popovich (The Ohio State University) for comments on the manuscript. We gratefully acknowledge support from the National Institutes of Health (R03NS078519 to OB; R01GM104123 to JJS; R01NS078165 to JRM), The Feinstein Institute for Medical Research and The Marine Biological Laboratory, including the Charles Evans Foundation Research Award, the Albert and Ellen Grass Foundation Faculty Research Award, and The Eugene and Millicent Bell Fellowship Fund in Tissue Engineering.

FinanciadoresNúmero del financiador
Albert and Ellen Grass Foundation
Charles Evans Foundation
Feinstein Institute for Medical Research
National Institutes of Health (NIH)R03NS078519, R01GM104123
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke CouncilR01NS078165
Marine Biological Laboratory

    ASJC Scopus subject areas

    • General

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