Skeletal tissues in Mozambique tilapia (Oreochromis mossambicus) express the extracellular calcium-sensing receptor

Comparative Biochemistry and Physiology - A Molecular and Integrative Physiology

Volumn 163, Issue 3-4, 2012, Pages 311-318

  Loretz, Christopher A ^a,b   Pollina, Catherine ^a,b   Herberger, Amanda L ^a   Hyodo, Susumu ^b   Takei, Yoshio ^b  

^a UNIVERSITY AT BUFFALO   (United States)

^b UNIVERSITY OF TOKYO   (Japan)

Author keywords

Bone; Calcium homeostasis; Extracellular calcium sensing receptor; Skeleton; Teleost fish; Tilapia

Indexed keywords

EXTRACELLULAR CALCIUM SENSING RECEPTOR; MESSENGER RNA; RECEPTOR; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BODY SURFACE; CALCIUM HOMEOSTASIS; CARTILAGE CELL; CASR GENE; GENE; GENE EXPRESSION; GENETIC ANALYSIS; HYALINE CARTILAGE; IMMUNOHISTOCHEMISTRY; NONHUMAN; OREOCHROMIS MOSSAMBICUS; OSTEOBLAST; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SCLEROBLAST; SKELETAL TISSUE;

CICHLIDAE; OREOCHROMIS MOSSAMBICUS; PISCES; TELEOSTEI; TILAPIA; VERTEBRATA;

EID: 84866419406     PISSN: 10956433     EISSN: 15314332     Source Type: Journal    
DOI: 10.1016/j.cbpa.2012.07.015     Document Type: Article

References (43)

1. Apschner A., Schulte-Merker S., Witten P.E. Not all bones are created equal-using zebrafish and other teleost species in osteogenesis research. Methods Cell Biol. 2011, 105:239-255. 10.1016/B978-0-12-381320-6.00010-2.
2. Bereiter-Hahn J., Zylberberg L. Regeneration of teleost fish scale. Comp. Biochem. Physiol. A Physiol. 1993, 105:625-641. 10.1016/0300-9629(93)90262-3.
3. Bodznick D. Calcium ion: an odorant for natural water discriminations and the migratory behavior of sockeye salmon. J. Comp. Physiol. A 1978, 127:157-166. 10.1007/BF01352300.
4. Brown E.M., MacLeod R.J. Extracellular calcium sensing and extracellular calcium signaling. Physiol. Rev. 2001, 81:239-297. (http://physrev.physiology.org/cgi/content/full/81/1/239).
5. Cao L., Moriishi T., Miyazaki T., Iimura T., Hamagaki M., Nakane A., Tamamura Y., Komori T., Yamaguchi A. Comparative morphology of the osteocyte lacunocanalicular system in various vertebrates. J. Bone Miner. Metab. 2011, 29:662-670. 10.1007/s00774-011-0268-6.
6. Chang W., Tu C., Chen T.-H., Komuves L., Oda Y., Pratt S.A., Miller S., Shoback D. Expression and signal transduction of calcium-sensing receptors in cartilage and bone. Endocrinology 1999, 140:5883-5893. (http://endo.endojournals.org/cgi/reprint/140/12/5883).
7. Chang W., Tu C., Bikle D., Shoback D. The extracellular calcium-sensing receptor (CaSR) is a critical modulator of skeletal development. Sci. Signal. 2008, 1(35):ra1. 10.1126/scisignal.1159945.
8. 2+-sensing receptor and cell differentiation in murine growth plate chondrocytes. Endocrinology 2007, 148:4984-4992. 10.1210/en.2007-0653.
9. Dal Pai-Silva M., Carvalho R.F., Pellizzon C.H., Dal Pai V. Muscle growth in Nile tilapia (Oreochromis niloticus): histochemical, ultrastructural and morphometric study. Tissue Cell 2003, 35:179-187. 10.1016/S0040-8166(03)00019-3.
10. Danks J.A., D'Souza D.G., Gunn H.J., Milley K.M., Richardson S.J. Evolution of the parathyroid hormone family and skeleton formation pathways. Gen. Comp. Endocrinol. 2011, 170:79-91. 10.1016/j.ygcen.2010.10.023.
11. Donoghue P.C.J., Sansom I.J. Origin and early evolution of vertebrate skeletonization. Microsc. Res. Tech. 2002, 59:352-372. 10.1002/jemt.10217.
12. Donoghue P.C.J., Sansom I.J., Downs J.P. Early evolution of vertebrate skeletal tissues and cellular interactions, and the canalization of skeletal development. J. Exp. Zool. 2006, 306B:278-294. 10.1002/jez.b.21090.
13. Dukes J.P., Deaville R., Gottelli D., Neigel J.E., Bruford M.W., Jordan W.C. Isolation and characterization of main olfactory and vomeronasal receptor gene families from the Atlantic salmon (Salmo salar). Gene 2006, 371:257-267. 10.1016/j.gene.2005.12.003.
14. 2+-sensing receptor regulates bone development, mineralization, and turnover. J. Bone Miner. Res. 2011, 26:2935-2947. 10.1002/jbmr.520.
15. Evans D.H., Piermarini P.M., Choe K.P. The multifunctional fish gill: dominant site of gas exchange, osmoregulation, acid-base regulation, and excretion of nitrogenous waste. Physiol. Rev. 2005, 85:97-177. 10.1152/physrev.00050.2003.
16. Flanagan J.A., Bendell L.A., Guerreiro P.M., Clark M.S., Power D.M., Canario A.V.M., Brown B.L., Ingleton P. Cloning of the cDNA for the putative calcium-sensing receptor and its tissue distribution in sea bream (Sparus aurata). Gen. Comp. Endocrinol. 2002, 127:117-127. 10.1016/S0016-6480(02)00035-7.
17. Fujimura K., Okada N. Bone development in the jaw of Nile tilapia Oreochromis niloticus (Pisces: Cichlidae). Dev. Growth Differ. 2008, 50:339-355. 10.1111/j.1440-169x.2008.01032.x.
18. Genten F., Terwinghe E., Danguy A. Atlas of Fish Histology 2009, Science Publishers, Enfield, NJ.
19. Hecht J., Stricker S., Wiecha U., Stiege A., Panopoulou G., Podsiadlowski L., Poustka A.J., Dieterich C., Ehrich S., Suvorova J., Mundlos S., Seitz V. Evolution of a core gene network for skeletogenesis in chordates. PLoS Genet. 2008, 4(3):e1000025. 10.1371/journal.pgen.1000025.
20. Herberger A., Loretz C.A. Examining phylogenetic history of the extracellular calcium-sensing receptor: a key sensor in calcium homeostatic systems. Front. Endocrin. 2011, 10.3389/conf.fendo.2011.04.00025.
21. Hubbard P.C., Canario A.V.M. Evidence that olfactory sensitivities to calcium and sodium are mediated by different mechanisms in the goldfish Carassius auratus. Neurosci. Lett. 2007, 414:90-93. 10.1016/j.neulet.2006.12.007.
22. 2+] in the marine teleost Sparus aurata. J. Exp. Biol. 2000, 203:3821-3829. (http://jeb.biologists.org/cgi/reprint/203/24/3821).
23. 2+-sensing receptor?. J. Exp. Biol. 2002, 205:2755-2764. (http://jeb.biologists.org/cgi/reprint/205/18/2755).
24. Loretz C.A. Extracellular calcium-sensing receptors in fishes. Comp. Biochem. Physiol. A: Molec. Integr. Physiol. 2008, 149:225-245. 10.1016/j.cbpa.2008.01.037.
25. 2+-sensing receptor with truncated carboxyterminal tail from the Mozambique tilapia (Oreochromis mossambicus). J. Biol. Chem. 2004, 279:53288-53297. (http://www.jbc.org/content/279/51/53288).
26. Loretz C.A., Pollina C., Hyodo S., Takei Y. Extracellular calcium-sensing receptor expression in osmoregulatory and endocrine tissues of the tilapia. Gen. Comp. Endocrinol. 2009, 161:216-228. 10.1016/j.ygcen.2008.12.020.
27. Loretz C.A., Pollina C., Herberger A.L., Hyodo S., Takei Y. Skeletal tissues in tilapia express the extracellular calcium-sensing receptor. FASEB J. 2011, 25:1048.1. (http://www.fasebj.org/cgi/content/meeting_abstract/25/1_MeetingAbstracts/1048.1).
28. 2+-sensing receptor in Fugu. Proc. Natl. Acad. Sci. U. S. A. 1998, 95:5178-5181. (http://www.pnas.org/cgi/reprint/95/9/5178).
29. Römpler H., Stäubert C., Thor D., Schulz A., Hofreiter M., Schöneberg T. G protein-coupled time travel: evolutionary aspects of GPCR research. Med. Intervent. 2007, 7:17-25. 10.1124/mi.7.1.5.
30. Rotllant J., Redruello B., Guerreiro P.M., Fernandes H., Canario A.V.M., Power D.M. Calcium mobilization from fish scales is mediated by parathyroid hormone related protein via the parathyroid hormone type 1 receptor. Reg. Peptides 2005, 132:33-40. 10.1016/j.regpep.2005.08.004.
31. Sire J.-Y., Huysseune A. Formation of dermal skeletal and dental tissues in fish: a comparative and evolutionary approach. Biol. Rev. 2003, 78:219-249. 10.1017/S1464793102006073.
32. Strotmann R., Schröck K., Böselt I., Stäubert C., Russ A., Schöneberg T. Evolution of GPCR: change and continuity. Mol. Cell. Endocrinol. 2011, 331:170-178. 10.1016/j.mce.2010.07.012.
33. Tfelt-Hansen J., Brown E.M. The calcium-sensing receptor in normal physiology and pathophysiology: a review. Crit. Rev. Clin. Lab. Sci. 2005, 42:35-70. 10.1080/10408360590886606.
34. Tu C.-L., Chang W., Bikle D.D. The extracellular calcium-sensing receptor is required for calcium-induced differentiation in human keratinocytes. J. Biol. Chem. 2001, 276:41079-41085. (http://www.jbc.org/content/276/44/41079).
35. Tu C.-L., Chang W., Bikle D.D. The role of the calcium-sensing receptor in regulating intracellular calcium handling in human epidermal keratinocytes. J. Invest. Dermatol. 2007, 127:1074-1083. 10.1038/sj.jid.5700633.
36. Tu C.-L., Chang W., Bikle D.D. The calcium-sensing receptor-dependent regulation of cell-cell adhesion and keratinocyte differentiation requires Rho and filamin A. J. Invest. Dermatol. 2011, 131:1119-1128. 10.1038/jid.2010.414.
37. Wada H. Origin and evolution of the vertebrate skeleton. Zool. Sci. 2010, 27:119-123. 10.2108/zsj.27.119.
38. Witten P.E. Enzyme histochemical characteristics of osteoblasts and mononucleated osteoclasts in a teleost fish with acellular bone (Oreochromis niloticus, Cichlidae). Cell Tissue Res. 1997, 287:591-599. 10.1007/s004410050782.
39. Witten P.E., Huysseune A. A comparative view on mechanisms and functions of skeletal remodeling in teleost fish, with special emphasis on osteoclasts and their function. Biol. Rev. 2009, 84:315-346. 10.1111/j.1469-185X.2009.00077.x.
40. Witten P.E., Huysseune A. The unobtrusive majority: mononucleated bone resorbing cells in teleost fish and mammals. J. Appl. Ichthyol. 2010, 26:225-229. 10.1111/j.1439-0426.2010.01410.x.
41. Witten P.E., Hansen A., Hall B.K. Features of mono- and multinucleated bone resorbing cells of the zebrafish Danio rerio and their contribution to skeletal development, remodeling, and growth. J. Morphol. 2001, 250:197-207. 10.1002/jmor.1065.
42. Witten P.E., Huysseune A., Hall B.K. A practical approach for the identification of the many cartilaginous tissues in teleost fish. J. Appl. Ichthyol. 2010, 26:257-262. 10.1111/j.1439-0426.2010.01416.x.
43. Zhang G., Eames B.F., Cohn M.J. Evolution of vertebrate cartilage development. Curr. Top. Dev. Biol. 2009, 86:15-42. 10.1016/S0070-2153(09)01002-3.