Literature DB >> 17977526

Position dependence of hemiray morphogenesis during tail fin regeneration in Danio rerio.

C Murciano1, J Pérez-Claros, A Smith, F Avaron, T D Fernández, I Durán, J Ruiz-Sánchez, F García, J Becerra, M-A Akimenko, M Marí-Beffa.   

Abstract

The fins of actinopterygian can regenerate following amputation. Classical papers have shown that the ray, a structural unit of these fins, might regenerate independent of this appendage. Each fin ray is formed by two apposed contralateral hemirays. A hemiray may autonomously regenerate and segmentate in a position-independent manner. This is observed when heterotopically grafted into an interray space, after amputation following extirpation of the contralateral hemiray or when simply ablated. During this process, a proliferating hemiblastema is formed, as shown by bromodeoxyuridine incorporation, from which the complete structure will regenerate. This hemiblastema shows a patterning of gene expression domain similar to half ray blastema. Interactions between contralateral hemiblastema have been studied by recombinant rays composed of hemirays from different origins on the proximo-distal or dorso-ventral axis of the caudal fin. Dye 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocianine perchlorate labeling of grafted tissues was used as tissular marker. Our results suggest both that there are contralateral interactions between hemiblastema of each ray, and that hemiblastema may vary its morphogenesis, always differentiating as their host region. These non-autonomous, position-dependent interactions control coordinated bifurcations, segment joints and ray length independently. A morphological study of the developing and regenerating fin of another long fin mutant zebrafish suggests that contralateral hemiblastema interactions are perturbed in this mutant.

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Year:  2007        PMID: 17977526     DOI: 10.1016/j.ydbio.2007.09.026

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  6 in total

1.  Widening control of fin inter-rays in zebrafish and inferences about actinopterygian fins.

Authors:  Carmen Murciano; Salvador Cazorla-Vázquez; Javier Gutiérrez; Juan Antonio Hijano; Josefa Ruiz-Sánchez; Laura Mesa-Almagro; Flores Martín-Reyes; Tahía Diana Fernández; Manuel Marí-Beffa
Journal:  J Anat       Date:  2018-02-14       Impact factor: 2.610

2.  Shh promotes direct interactions between epidermal cells and osteoblast progenitors to shape regenerated zebrafish bone.

Authors:  Benjamin E Armstrong; Astra Henner; Scott Stewart; Kryn Stankunas
Journal:  Development       Date:  2017-04-01       Impact factor: 6.868

Review 3.  Bioelectric signaling as a unique regulator of development and regeneration.

Authors:  Matthew P Harris
Journal:  Development       Date:  2021-05-17       Impact factor: 6.868

Review 4.  Dermoskeleton morphogenesis in zebrafish fins.

Authors:  Manuel Marí-Beffa; Carmen Murciano
Journal:  Dev Dyn       Date:  2010-11       Impact factor: 3.780

5.  Bioelectric signaling regulates size in zebrafish fins.

Authors:  Simon Perathoner; Jacob M Daane; Ulrike Henrion; Guiscard Seebohm; Charles W Higdon; Stephen L Johnson; Christiane Nüsslein-Volhard; Matthew P Harris
Journal:  PLoS Genet       Date:  2014-01-16       Impact factor: 5.917

6.  A new zebrafish bone crush injury model.

Authors:  Sara Sousa; Fabio Valerio; Antonio Jacinto
Journal:  Biol Open       Date:  2012-07-30       Impact factor: 2.422

  6 in total

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