Literature DB >> 15547792

The origin and evolution of the surfactant system in fish: insights into the evolution of lungs and swim bladders.

Christopher B Daniels1, Sandra Orgeig, Lucy C Sullivan, Nicholas Ling, Michael B Bennett, Samuel Schürch, Adalberto Luis Val, Colin J Brauner.   

Abstract

Several times throughout their radiation fish have evolved either lungs or swim bladders as gas-holding structures. Lungs and swim bladders have different ontogenetic origins and can be used either for buoyancy or as an accessory respiratory organ. Therefore, the presence of air-filled bladders or lungs in different groups of fishes is an example of convergent evolution. We propose that air breathing could not occur without the presence of a surfactant system and suggest that this system may have originated in epithelial cells lining the pharynx. Here we present new data on the surfactant system in swim bladders of three teleost fish (the air-breathing pirarucu Arapaima gigas and tarpon Megalops cyprinoides and the non-air-breathing New Zealand snapper Pagrus auratus). We determined the presence of surfactant using biochemical, biophysical, and morphological analyses and determined homology using immunohistochemical analysis of the surfactant proteins (SPs). We relate the presence and structure of the surfactant system to those previously described in the swim bladders of another teleost, the goldfish, and those of the air-breathing organs of the other members of the Osteichthyes, the more primitive air-breathing Actinopterygii and the Sarcopterygii. Snapper and tarpon swim bladders are lined with squamous and cuboidal epithelial cells, respectively, containing membrane-bound lamellar bodies. Phosphatidylcholine dominates the phospholipid (PL) profile of lavage material from all fish analyzed to date. The presence of the characteristic surfactant lipids in pirarucu and tarpon, lamellar bodies in tarpon and snapper, SP-B in tarpon and pirarucu lavage, and SPs (A, B, and D) in swim bladder tissue of the tarpon provide strong evidence that the surfactant system of teleosts is homologous with that of other fish and of tetrapods. This study is the first demonstration of the presence of SP-D in the air-breathing organs of nonmammalian species and SP-B in actinopterygian fishes. The extremely high cholesterol/disaturated PL and cholesterol/PL ratios of surfactant extracted from tarpon and pirarucu bladders and the poor surface activity of tarpon surfactant are characteristics of the surfactant system in other fishes. Despite the paraphyletic phylogeny of the Osteichthyes, their surfactant is uniform in composition and may represent the vertebrate protosurfactant.

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Year:  2004        PMID: 15547792     DOI: 10.1086/422058

Source DB:  PubMed          Journal:  Physiol Biochem Zool        ISSN: 1522-2152            Impact factor:   2.247


  22 in total

1.  Changes in Nkx2.1, Sox2, Bmp4, and Bmp16 expression underlying the lung-to-gas bladder evolutionary transition in ray-finned fishes.

Authors:  Emily C Funk; Catriona Breen; Bhargav D Sanketi; Natasza Kurpios; Amy McCune
Journal:  Evol Dev       Date:  2020-09       Impact factor: 1.930

2.  Chronic zebrafish PFOS exposure alters sex ratio and maternal related effects in F1 offspring.

Authors:  Mingyong Wang; Jiangfei Chen; Kuanfei Lin; Yuanhong Chen; Wei Hu; Robert L Tanguay; Changjiang Huang; Qiaoxiang Dong
Journal:  Environ Toxicol Chem       Date:  2011-06-30       Impact factor: 3.742

3.  The transcription factor Atonal homolog 8 regulates Gata4 and Friend of Gata-2 during vertebrate development.

Authors:  David R Rawnsley; Jiping Xiao; John S Lee; Xi Liu; Patricia Mericko-Ishizuka; Vinayak Kumar; Jie He; Arindam Basu; MinMin Lu; Francis C Lynn; Michael Pack; Rosa Gasa; Mark L Kahn
Journal:  J Biol Chem       Date:  2013-07-08       Impact factor: 5.157

Review 4.  Lung endoderm morphogenesis: gasping for form and function.

Authors:  Daniel T Swarr; Edward E Morrisey
Journal:  Annu Rev Cell Dev Biol       Date:  2015-09-10       Impact factor: 13.827

5.  Autophagy Is Required for Maturation of Surfactant-Containing Lamellar Bodies in the Lung and Swim Bladder.

Authors:  Hideaki Morishita; Yuki Kanda; Takeshi Kaizuka; Haruka Chino; Kazuki Nakao; Yoshimi Miki; Yoshitaka Taketomi; Jun-Lin Guan; Makoto Murakami; Atsu Aiba; Noboru Mizushima
Journal:  Cell Rep       Date:  2020-12-08       Impact factor: 9.423

Review 6.  The Lung and Esophagus: Developmental and Regenerative Overlap.

Authors:  Edward E Morrisey; Anil K Rustgi
Journal:  Trends Cell Biol       Date:  2018-06-02       Impact factor: 20.808

7.  Exploiting cellular-developmental evolution as the scientific basis for preventive medicine.

Authors:  J S Torday; V K Rehan
Journal:  Med Hypotheses       Date:  2009-01-14       Impact factor: 1.538

8.  Dorsoventral inversion of the air-filled organ (lungs, gas bladder) in vertebrates: RNAsequencing of laser capture microdissected embryonic tissue.

Authors:  Emily Funk; Ezra Lencer; Amy McCune
Journal:  J Exp Zool B Mol Dev Evol       Date:  2020-08-30       Impact factor: 2.656

9.  Why Do We have to Move Fluid to be Able to Breathe?

Authors:  Martin Fronius; Wolfgang G Clauss; Mike Althaus
Journal:  Front Physiol       Date:  2012-05-22       Impact factor: 4.566

10.  Evolution of the lung surfactant proteins in birds and mammals.

Authors:  Austin L Hughes
Journal:  Immunogenetics       Date:  2007-04-25       Impact factor: 3.330

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