期刊论文详细信息
BMC Developmental Biology
Functional modifications associated with gastrointestinal tract organogenesis during metamorphosis in Atlantic halibut (Hippoglossus hippoglossus)
Ivar Rønnestad2  Deborah M Power3  Torstein Harboe1  Yuko Kamisaka2  Ana S Gomes2 
[1]Institute of Marine Research, Austevoll Aquaculture Research Station, NO-5392 Storebø, Norway
[2]Department of Biology, University of Bergen, Po. Box 7803, NO-5020 Bergen, Norway
[3]Comparative and Molecular Endocrinology Group, Centre for Marine Sciences (CCMAR), University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal
关键词: Stomach;    pH;    Ontogeny;    Pepsinogen;    Na+/K+-ATPase;    Motility;    Ghrelin;    Gastrointestinal tract;    Gastric proton pump;    Atlantic halibut;   
Others  :  1085137
DOI  :  10.1186/1471-213X-14-11
 received in 2013-07-25, accepted in 2013-12-09,  发布年份 2014
PDF
【 摘 要 】

Background

Flatfish metamorphosis is a hormone regulated post-embryonic developmental event that transforms a symmetric larva into an asymmetric juvenile. In altricial-gastric teleost fish, differentiation of the stomach takes place after the onset of first feeding, and during metamorphosis dramatic molecular and morphological modifications of the gastrointestinal (GI-) tract occur. Here we present the functional ontogeny of the developing GI-tract from an integrative perspective in the pleuronectiforme Atlantic halibut, and test the hypothesis that the multiple functions of the teleost stomach develop synchronously during metamorphosis.

Results

Onset of gastric function was determined with several approaches (anatomical, biochemical, molecular and in vivo observations). In vivo pH analysis in the GI-tract lumen combined with quantitative PCR (qPCR) of α and β subunits of the gastric proton pump (H+/K+-ATPase) and pepsinogen A2 indicated that gastric proteolytic capacity is established during the climax of metamorphosis. Transcript abundance of ghrelin, a putative orexigenic signalling molecule produced in the developing stomach, correlated (p < 0.05) with the emergence of gastric proteolytic activity, suggesting that the stomach’s role in appetite regulation occurs simultaneously with the establishment of proteolytic function. A 3D models series of the GI-tract development indicated a functional pyloric sphincter prior to first feeding. Observations of fed larvae in vivo confirmed that stomach reservoir function was established before metamorphosis, and was thus independent of this event. Mechanical breakdown of food and transportation of chyme through the GI-tract was observed in vivo and resulted from phasic and propagating contractions established well before metamorphosis. The number of contractions in the midgut decreased at metamorphic climax synchronously with establishment of the stomach’s proteolytic capacity and its increased peristaltic activity. Putative osmoregulatory competence of the GI-tract, inferred by abundance of Na+/K+-ATPase α transcripts, was already established at the onset of exogenous feeding and was unmodified by metamorphosis.

Conclusions

The functional specialization of the GI-tract was not exclusive to metamorphosis, and its osmoregulatory capacity and reservoir function were established before first feeding. Nonetheless, acid production and the proteolytic capacity of the stomach coincided with metamorphic climax, and also marked the onset of the stomach’s involvement in appetite regulation via ghrelin.

【 授权许可】

   
2014 Gomes et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150113170953911.pdf 2438KB PDF download
Figure 7. 67KB Image download
Figure 6. 185KB Image download
Figure 5. 46KB Image download
Figure 4. 61KB Image download
Figure 3. 59KB Image download
Figure 2. 151KB Image download
Figure 1. 143KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

Figure 4.

Figure 5.

Figure 6.

Figure 7.

【 参考文献 】
  • [1]Smith DM, Grasty RC, Theodosiou NA, Tabin CJ, Nascone-Yoder NM: Evolutionary relationships between the amphibian, avian, and mammalian stomachs. Evol Dev 2000, 2(6):348-359.
  • [2]Laudet V: The origins and evolution of vertebrate metamorphosis. Curr Biol 2011, 21(18):R726-737.
  • [3]Power DM, Einarsdóttir IE, Pittman K, Sweeney GE, Hildahl J, Campinho MA, Silva N, Sæle Ø, Galay-Burgos M, Smáradóttir H, Björnsson BT: The molecular and endocrine basis of flatfish metamorphosis. Rev Fish Sci 2008, 16(1):95-111.
  • [4]Brown DD, Cai L: Amphibian metamorphosis. Dev Biol 2007, 306(1):20-33.
  • [5]Ishizuya-Oka A, Inokuchi T, Ueda S: Thyroid hormone-induced apoptosis of larval cells and differentiation of pepsinogen-producing cells in the stomach of Xenopus laevis in vitro. Differentiation 1998, 63(2):59-68.
  • [6]Ishizuya-Oka A, Shi YB: Molecular mechanisms for thyroid hormone-induced remodeling in the amphibian digestive tract: a model for studying organ regeneration. Dev Growth Differ 2005, 47(9):601-607.
  • [7]Schreiber AM, Mukhi S, Brown DD: Cell–cell interactions during remodeling of the intestine at metamorphosis in Xenopus laevis. Dev Biol 2009, 331(1):89-98.
  • [8]Ishizuya-Oka A: Amphibian organ remodeling during metamorphosis: insight into thyroid hormone-induced apoptosis. Dev Growth Differ 2011, 53(2):202-212.
  • [9]Stevens CE, Hume ID: Comparative physiology of the vertebrate digestive system. Cambridge, UK: Cambridge University Press; 2004.
  • [10]Govoni J, Boehlert G, Watanabe Y: The physiology of digestion in fish larvae. Environ Biol Fish 1986, 16(1–3):59-77.
  • [11]Segner H, Storch V, Reinecke M, Kloas W, Hanke W: The development of functional digestive and metabolic organs in turbot. Scophthalmus maximus. Mar Biol 1994, 119(3):471-486.
  • [12]Rust MB: Quantitative aspects of nutrient assimilation in six species of fish larva. Seattle, USA: Washington University, School of Fisheries; 1995. [PhD thesis]
  • [13]Tonheim SK, Espe M, Hamre K, Rønnestad I: Pre-hydrolysis improves utilisation of dietary protein in the larval teleost Atlantic halibut (Hippoglossus hippoglossus L.). J Exp Mar Biol Ecol 2005, 321(1):19-34.
  • [14]Rønnestad I, Yúfera M, Ueberschär B, Ribeiro L, Sæle Ø, Boglione C: Feeding behaviour and digestive physiology in larval fish: current knowledge, and gaps and bottlenecks in research. Rev Aquaculture 2013, 5(1):S59-S98.
  • [15]Tanaka M: Studies on the structure and function of the digestive system of teleost larvae. Kyoto, Japan: Kyoto University, Department of Fisheries; 1973. [PhD thesis]
  • [16]Murray HM, Wright GM, Goff GP: A comparative histological and histochemical study of the stomach from three species of pleuronectid, the Atlantic halibut, Hippoglossus hippoglossus, the yellowtail flounder, Pleuronectes ferruginea, and the winter flounder, Pleuronectes americanus. Can J Zool 1994, 72(7):1199-1210.
  • [17]Moyano FJ, Díaz M, Alarcón FJ, Sarasquete MC: Characterization of digestive enzyme activity during larval development of gilthead seabream (Sparus aurata). Fish Physiol Biochem 1996, 15(2):121-130.
  • [18]Huang L, Schreiber AM, Soffientino B, Bengtson DA, Specker JL: Metamorphosis of summer flounder (Paralichthys dentatus): thyroid status and the timing of gastric gland formation. J Exp Zool 1998, 280(6):413-420.
  • [19]Douglas SE, Gawlicka A, Mandla S, Gallant JW: Ontogeny of the stomach in winter flounder: characterization and expression of the pepsinogen and proton pump genes and determination of pepsin activity. J Fish Biol 1999, 55(5):897-915.
  • [20]Gawlicka A, Leggiadro CT, Gallant JW, Douglas SE: Cellular expression of the pepsinogen and gastric proton pump genes in the stomach of winter flounder as determined by in situ hybridization. J Fish Biol 2001, 58(2):529-536.
  • [21]Darias MJ, Murray HM, Gallant JW, Douglas SE, Yúfera M, Martínez-Rodríguez G: Ontogeny of pepsinogen and gastric proton pump expression in red porgy (Pagrus pagrus): determination of stomach functionality. Aquaculture 2007, 270(1–4):369-378.
  • [22]Yúfera M, Moyano FJ, Astola A, Pousão-Ferreira P, Martínez-Rodríguez G: Acidic digestion in a Teleost: postprandial and circadian pattern of gastric pH, pepsin activity, and pepsinogen and proton pump mRNAs expression. PLoS ONE 2012, 7(3):e33687.
  • [23]Murray HM, Gallant JW, Johnson SC, Douglas SE: Cloning and expression analysis of three digestive enzymes from Atlantic halibut (Hippoglossus hippoglossus) during early development: predicting gastrointestinal functionality. Aquaculture 2006, 252(2–4):394-408.
  • [24]Olsson C, Holmgren S: The control of gut motility. Comp Biochem Physiol, Part A: Mol Integr Physiol 2001, 128(3):479-501.
  • [25]Pittman K, Skiftesvik AB, Berg L: Morphological and behavioural development of halibut, Hippoglossus hippoglossus (L.) larvae. J Fish Biol 1990, 37(3):455-472.
  • [26]Rønnestad I, Rojas-Garcia CR, Skadal J: Retrograde peristalsis; a possible mechanism for filling the pyloric caeca? J Fish Biol 2000, 56(1):216-218.
  • [27]Holmberg A, Schwerte T, Fritsche R, Pelster B, Holmgren S: Ontogeny of intestinal motility in correlation to neuronal development in zebrafish embryos and larvae. J Fish Biol 2003, 63(2):318-331.
  • [28]Date Y, Kojima M, Hosoda H, Sawaguchi A, Mondal MS, Suganuma T, Matsukura S, Kangawa K, Nakazato M: Ghrelin, a novel growth hormone-releasing acylated peptide, is synthesized in a distinct endocrine cell type in the gastrointestinal tracts of rats and humans. Endocrinology 2000, 141(11):4255-4261.
  • [29]Nakazato M, Murakami N, Date Y, Kojima M, Matsuo H, Kangawa K, Matsukura S: A role for ghrelin in the central regulation of feeding. Nature 2001, 409(6817):194-198.
  • [30]Masuda Y, Tanaka T, Inomata N, Ohnuma N, Tanaka S, Itoh Z, Hosoda H, Kojima M, Kangawa K: Ghrelin stimulates gastric acid secretion and motility in rats. Biochem Biophys Res Commun 2000, 276(3):905-908.
  • [31]Fujitsuka N, Asakawa A, Amitani H, Fujimiya M, Inui A: Methods in enzymology: volume 514. Edited by Masayasu K, Kenji K. San Diego: Academic Press; 2012:289-301.
  • [32]Xu M, Volkoff H: Molecular characterization of ghrelin and gastrin-releasing peptide in Atlantic cod (Gadus morhua): cloning, localization, developmental profile and role in food intake regulation. Gen Comp Endocrinol 2009, 160(3):250-258.
  • [33]Manning AJ, Murray HM, Gallant JW, Matsuoka MP, Radford E, Douglas SE: Ontogenetic and tissue-specific expression of preproghrelin in the Atlantic halibut, Hippoglossus hippoglossus L. J Endocrinol 2008, 196(1):181-192.
  • [34]Einarsdóttir I, Power D, Jönsson E, Björnsson B: Occurrence of ghrelin-producing cells, the ghrelin receptor and Na+, K + −ATPase in tissues of Atlantic halibut (Hippoglossus hippoglossus) during early development. Cell Tissue Res 2011, 344(3):481-498.
  • [35]Schreiber AM, Cai L, Brown DD: Remodeling of the intestine during metamorphosis of Xenopus laevis. Proc Natl Acad Sci U S A 2005, 102(10):3720-3725.
  • [36]Ishizuya-Oka A, Ueda S, Damjanovski S, Li Q, Liang VCT, Shi Y-B: Anteroposterior gradient of epithelial transformation during amphibian intestinal remodeling: immunohistochemical detection of intestinal fatty acid-binding protein. Dev Biol 1997, 192(1):149-161.
  • [37]Ishizuya-Oka A, Ueda S: Apoptosis and cell proliferation in the Xenopus small intestine during metamorphosis. Cell Tissue Res 1996, 286(3):467-476.
  • [38]Ishizuya-Oka A, Ueda S, Inokuchi T, Amano T, Damjanovski S, Stolow M, Shi YB: Thyroid hormone-induced expression of sonic hedgehog correlates with adult epithelial development during remodeling of the Xenopus stomach and intestine. Differentiation 2001, 69(1):27-37.
  • [39]Ishizuya-Oka A, Shi YB: Regulation of adult intestinal epithelial stem cell development by thyroid hormone during Xenopus laevis metamorphosis. Dev Dyn 2007, 236(12):3358-3368.
  • [40]Ishizuya-Oka A, Hasebe T, Shimizu K, Suzuki K, Ueda S: Shh/BMP-4 signaling pathway is essential for intestinal epithelial development during Xenopus larval-to-adult remodeling. Dev Dyn 2006, 235(12):3240-3249.
  • [41]Galay-Burgos M, Power DM, Llewellyn L, Sweeney GE: Thyroid hormone receptor expression during metamorphosis of Atlantic halibut (Hippoglossus hippoglossus). Mol Cell Endocrinol 2008, 281(1–2):56-63.
  • [42]Yaoita Y, Brown DD: A correlation of thyroid hormone receptor gene expression with amphibian metamorphosis. Genes Dev 1990, 4(11):1917-1924.
  • [43]Kamisaka Y, Rønnestad I: Reconstructed 3D models of digestive organs of developing Atlantic cod (Gadus morhua) larvae. Mar Biol 2011, 158(1):233-243.
  • [44]Rønnestad I, Yúfera M, Ueberschär B, Ribeiro L, Sæle Ø, Boglione C: Feeding behaviour and digestive physiology in larval fish: current knowledge, and gaps and bottlenecks in research. Rev Aquaculture 2013, 5:S59-S98.
  • [45]Miwa S, Yamano K, Inui Y: Thyroid hormone stimulates gastric development in flounder larvae during metamorphosis. J Exp Zool 1992, 261(4):424-430.
  • [46]Maeda M: Gastric proton pump (H+/K(+)-ATPase): structure and gene regulation through GATA DNA-binding protein(s). J Biochem 1994, 115(1):6-14.
  • [47]Shin JM, Besancon M, Bamberg K, Sachs G: Structural aspects of the gastric H, K ATPase. Ann N Y Acad Sci 1997, 834:65-76.
  • [48]Shin JM, Munson K, Vagin O, Sachs G: The gastric HK-ATPase: structure, function, and inhibition. Pflugers Arch, EJP 2009, 457(3):609-622.
  • [49]Morley GP, Callaghan JM, Rose JB, Toh BH, Gleeson PA, van Driel IR: The mouse gastric H, K-ATPase beta subunit: gene structure and co-ordinate expression with the alpha subunit during ontogeny. J Biol Chem 1992, 267(2):1165-1174.
  • [50]Darias MJ, Murray HM, Martínez-Rodríguez G, Cárdenas S, Yúfera M: Gene expression of pepsinogen during the larval development of red porgy (Pagrus pagrus). Aquaculture 2005, 248(1–4):245-252.
  • [51]Gao C, Yang RB, Hu WB, Wang J: Ontogeny of the stomach in yellow catfish (Pelteobagrus fulvidraco): detection and quantifictation of pepsinogen and H+/K + −ATPase gene expression. J Anim Physiol Anim Nutr (Berl) 2013, 97(1):20-26.
  • [52]Bal HS, Ghoshal NG: Electron microscopy of the oxynticopeptic cells of the gastric glands and the intestinal glands of the caecum of the guineapig. Lab Anim 1992, 26(1):47-52.
  • [53]Rønnestad I, Dominguez RP, Tanaka M: Ontogeny of digestive tract functionality in Japanese flounder, Paralichthys olivaceus studied by in vivo microinjection: pH and assimilation of free amino acids. Fish Physiol Biochem 2000, 22(3):225-235.
  • [54]Walford J, Lam TJ: Development of digestive tract and proteolytic enzyme activity in seabass (Lates calcarifer) larvae and juveniles. Aquaculture 1993, 109(2):187-205.
  • [55]Hoehne-Reitan K, Kjørsvik E, Reitan K: Development of the pH in the intestinal tract of larval turbot. Mar Biol 2001, 139(6):1159-1164.
  • [56]Yúfera M, Fernández-Díaz C, Vidaurreta A, Cara JB, Moyano FJ: Gastrointestinal pH and development of the acid digestion in larvae and early juveniles of Sparus aurata (Pisces: Teleostei). Mar Biol 2004, 144(5):863-869.
  • [57]Grosell M: Intestinal anion exchange in marine fish osmoregulation. J Exp Biol 2006, 209(Pt 15):2813-2827.
  • [58]Grosell M, Taylor JR: Intestinal anion exchange in teleost water balance. Comp Biochem Physiol, Part A: Mol Integr Physiol 2007, 148(1):14-22.
  • [59]Taylor JR, Grosell M: Feeding and osmoregulation: dual function of the marine teleost intestine. J Exp Biol 2006, 209(Pt 15):2939-2951.
  • [60]Du G-M, Liu M-J, Shi Z-M, Zhang L, Wei X-H, Zhao R-Q: In vitro effects of ghrelin on gastric H + −K + −ATPase and pepsin activity and mRNA expression of gastrin, somatostatin, receptors for GH and IGF-1 in cultured gastric mucosal cells of weanling piglets. Anim Sci 2006, 82(06):823-828.
  • [61]Horn MH, Messer KS: Fish guts as chemical reactors: a model of the alimentary canals of marine herbivorous fishes. Mar Biol 1992, 113(4):527-535.
  • [62]Kamisaka Y, Totland GK, Tagawa M, Kurokawa T, Suzuki T, Tanaka M, Rønnestad I: Ontogeny of cholecystokinin-immunoreactive cells in the digestive tract of Atlantic halibut, Hippoglossus hippoglossus. Larvae. Gen Comp Endocrinol 2001, 123(1):31-37.
  • [63]Harboe T, Mangor-Jensen A, Moren M, Hamre K, Rønnestad I: Control of light condition affects the feeding regime and enables successful eye migration in Atlantic halibut juveniles. Aquaculture 2009, 290(3–4):250-255.
  • [64]Sæle Ø, Solbakken JS, Watanabe K, Hamre K, Power D, Pittman K: Staging of Atlantic halibut (Hippoglossus hippoglossus L.) from first feeding through metamorphosis, including cranial ossification independent of eye migration. Aquaculture 2004, 239(1–4):445-465.
  • [65]Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG: The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 1997, 25(24):4876-4882.
  • [66]Jones DT, Taylor WR, Thornton JM: The rapid generation of mutation data matrices from protein sequences. Comput Appl Biosci 1992, 8(3):275-282.
  • [67]Felsenstein J: Confidence limits on phylogenies: an approach using the bootstrap. Evolution 1985, 39(4):783-791.
  • [68]Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S: MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 2011, 28(10):2731-2739.
  • [69]Infante C, Matsuoka MP, Asensio E, Canavate JP, Reith M, Manchado M: Selection of housekeeping genes for gene expression studies in larvae from flatfish using real-time PCR. BMC Mol Biol 2008, 9:28. BioMed Central Full Text
  • [70]Muller PY, Janovjak H, Miserez AR, Dobbie Z: Processing of gene expression data generated by quantitative real-time RT-PCR. Biotechniques 2002, 32(6):1372-1374. 1376, 1378–1379
  • [71]Simon P: Q-gene: processing quantitative real-time RT-PCR data. Bioinformatics 2003, 19(11):1439-1440.
  • [72]Chambers JM: Chapter 4: linear models. In Statistical models in S. Edited by Chambers JM, Hastie TJ. California: Wadsworth & Brooks/Cole; 1992.
  • [73]Wilkinson GN, Rogers CE: Symbolic descriptions of factorial models for analysis of variance. J Roy Statist Soc Ser C 1973, 22:392-399.
  • [74]R: Development Core Team: R: a language and environment for statistical computing. Vienna, Austria: Foundation for Statistical Computing; 2013.
  • [75]Ottoni E: EthoLog 2.2: a tool for the transcription and timing of behavior observation sessions. Behav Res Methods Instrum Comput 2000, 32(3):446-449.
  文献评价指标  
  下载次数:86次 浏览次数:20次