Reversion to developmental pathways underlies rapid arm regeneration in juvenile European cuttlefish, Sepia officinalis (Linnaeus 1758).

amputation cephalopod cuttlefish development immune progenitor regeneration

Journal

Journal of experimental zoology. Part B, Molecular and developmental evolution
ISSN: 1552-5015
Titre abrégé: J Exp Zool B Mol Dev Evol
Pays: United States
ID NLM: 101168228

Informations de publication

Date de publication:
05 2019
Historique:
received: 13 09 2018
revised: 18 01 2019
accepted: 06 03 2019
pubmed: 20 3 2019
medline: 19 2 2020
entrez: 20 3 2019
Statut: ppublish

Résumé

Coleoid cephalopods, including the European cuttlefish (Sepia officinalis), possess the remarkable ability to fully regenerate an amputated arm with no apparent fibrosis or loss of function. In model organisms, regeneration usually occurs as the induction of proliferation in differentiated cells. In rare circumstances, regeneration can be the product of naïve progenitor cells proliferating and differentiating de novo . In any instance, the immune system is an important factor in the induction of the regenerative response. Although the wound response is well-characterized, little is known about the physiological pathways utilized by cuttlefish to reconstruct a lost arm. In this study, the regenerating arms of juvenile cuttlefish, with or without exposure at the time of injury to sterile bacterial lipopolysaccharide extract to provoke an antipathogenic immune response, were assessed for the transcription of early tissue lineage developmental genes, as well as histological and protein turnover analyses of the resulting regenerative process. The transient upregulation of tissue-specific developmental genes and histological characterization indicated that coleoid arm regeneration is a stepwise process with staged specification of tissues formed de novo, with immune activation potentially affecting the timing but not the result of this process. Together, the data suggest that rather than inducing proliferation of mature cells, developmental pathways are reinstated, and that a pool of naïve progenitors at the blastema site forms the basis for this regeneration.

Identifiants

pubmed: 30888729
doi: 10.1002/jez.b.22849
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

113-120

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Neal I Callaghan (NI)

Institute of Biomaterials and Biomedical Engineering, Faculty of Applied Science and Engineering, University of Toronto, Toronto, ON, Canada.
Translational Biology and Engineering Program, Ted Rogers Centre for Heart Research, Toronto, ON, Canada.

Juan C Capaz (JC)

CCMAR - Centro de Ciências do Mar do Algarve, Universidade do Algarve, Campus de Gambelas, Faro, Portugal.

Simon G Lamarre (SG)

Department of Biology, University of Moncton, Moncton, NB, Canada.

Émilie Bourloutski (É)

Department of Biology, University of Moncton, Moncton, NB, Canada.

Ana R Oliveira (AR)

CCMAR - Centro de Ciências do Mar do Algarve, Universidade do Algarve, Campus de Gambelas, Faro, Portugal.

Tyson J MacCormack (TJ)

Department of Chemistry and Biochemistry, Mount Allison University, Sackville, NB, Canada.

William R Driedzic (WR)

Department of Ocean Sciences, Memorial University of Newfoundland, St. John's, NL, Canada.

Antonio V Sykes (AV)

CCMAR - Centro de Ciências do Mar do Algarve, Universidade do Algarve, Campus de Gambelas, Faro, Portugal.

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Classifications MeSH