Literature DB >> 26108341

Carbonic anhydrase inhibition blocks skeletogenesis and echinochrome production in Paracentrotus lividus and Heliocidaris tuberculata embryos and larvae.

Francesca Zito1, Demian Koop2, Maria Byrne2, Valeria Matranga1.   

Abstract

Carbonic anhydrases (CAs) are a family of widely distributed metalloenzymes, involved in diverse physiological processes. These enzymes catalyse the reversible conversion of carbon dioxide to protons and bicarbonate. At least 19 genes encoding for CAs have been identified in the sea urchin genome, with one of these localized to the skeletogenic mesoderm (primary mesenchyme cells, PMCs). We investigated the effects of a specific inhibitor of CA, acetazolamide (AZ), on development of two sea urchin species with contrasting investment in skeleton production, Paracentrotus lividus and Heliocidaris tuberculata, to determine the role of CA on PMC differentiation, skeletogenesis and on non-skeletogenic mesodermal (NSM) cells. Embryos were cultured in the presence of AZ from the blastula stage prior to skeleton formation and development to the larval stage was monitored. At the dose of 8 mmol/L AZ, 98% and 90% of P. lividus and H. tuberculata embryos lacked skeleton, respectively. Nevertheless, an almost normal PMC differentiation was indicated by the expression of msp130, a PMC-specific marker. Strikingly, the AZ-treated embryos also lacked the echinochrome pigment produced by the pigment cells, a subpopulation of NSM cells with immune activities within the larva. Conversely, all ectoderm and endoderm derivatives and other subpopulations of mesoderm developed normally. The inhibitory effects of AZ were completely reversed after removal of the inhibitor from the medium. Our data, together with new information concerning the involvement of CA on skeleton formation, provide evidence for the first time of a possible role of the CAs in larval immune pigment cells.
© 2015 Japanese Society of Developmental Biologists.

Entities:  

Keywords:  acetazolamide; biomineralization; larval immune pigment cells; primary mesenchyme cells; sea urchin

Mesh:

Substances:

Year:  2015        PMID: 26108341     DOI: 10.1111/dgd.12229

Source DB:  PubMed          Journal:  Dev Growth Differ        ISSN: 0012-1592            Impact factor:   2.053


  5 in total

1.  Rare genetic variation and balanced polymorphisms are important for survival in global change conditions.

Authors:  Reid S Brennan; April D Garrett; Kaitlin E Huber; Heidi Hargarten; Melissa H Pespeni
Journal:  Proc Biol Sci       Date:  2019-06-12       Impact factor: 5.349

Review 2.  From genome to anatomy: The architecture and evolution of the skeletogenic gene regulatory network of sea urchins and other echinoderms.

Authors:  Tanvi Shashikant; Jian Ming Khor; Charles A Ettensohn
Journal:  Genesis       Date:  2018-10       Impact factor: 2.487

3.  Characterization of an Alpha Type Carbonic Anhydrase from Paracentrotus lividus Sea Urchin Embryos.

Authors:  Konstantinos Karakostis; Caterina Costa; Francesca Zito; Franz Brümmer; Valeria Matranga
Journal:  Mar Biotechnol (NY)       Date:  2016-05-26       Impact factor: 3.619

4.  Functional Involvement of Carbonic Anhydrase in the Lysosomal Response to Cadmium Exposure in Mytilus galloprovincialis Digestive Gland.

Authors:  Roberto Caricato; M Elena Giordano; Trifone Schettino; M Giulia Lionetto
Journal:  Front Physiol       Date:  2018-04-04       Impact factor: 4.566

Review 5.  Toxicological Impact of Rare Earth Elements (REEs) on the Reproduction and Development of Aquatic Organisms Using Sea Urchins as Biological Models.

Authors:  Chiara Martino; Teresa Chianese; Roberto Chiarelli; Maria Carmela Roccheri; Rosaria Scudiero
Journal:  Int J Mol Sci       Date:  2022-03-06       Impact factor: 5.923

  5 in total

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