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Histochemical studies of Ca-ATPase, succinate and NAD+-dependent isocitrate dehydrogenases in the shell gland of laying Japanese quails: with special reference to calcium-transporting cells

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Summary

In order to elucidate the problem of which cells are involved in calcium transport and to estimate the role of mitochondria in calcium transport in the avian shell gland, the fine structure and the Ca-ATPase, succinate dehydrogenase (SDH) and nicotinamide adenine dinucleotide (NAD+)-dependent isocitrate dehydrogenase (NAD+-ICDH) activity of the shell gland of egg-laying Japanese quails were examined. The surface epithelial cells, consisting of ciliated cells with cilia and microvilli and non-ciliated cells with microvilli, had many large and electron-dense granules. The tubular-gland cells occupied the proprial layer and lacked secretory granules. When an egg was in the shell gland, the well-developed mitochondria of tubular-gland cells characteristically tended to accumulate in the apical cytoplasm, while they were scattered throughout the cytoplasm when an egg was not in the shell gland. Intense Ca-ATPase activity was found on the microvilli of tubular-gland cells, and moderate activity was found on the lateral-cell surface. In the surface epithelial cells, the basolateral cell surface showed moderate enzymatic activity. Both SDH and NAD+-ICDH activity were found in tubular-gland cells when an egg was in the shell gland. These results strongly suggest that calcium for eggshell calcification is actively transported by the tubular-gland (depending on Ca-ATPase activity) and that the mitochondria of gland cells may play an important role in this process as an energy source.

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References

  • Aitken RNC (1972) The oviduct. In: Bell DJ, Freeman BM (eds) Physiology and biochemistry of the domestic fowl, vol 3. Academic Press, London New York, pp 1237–1389

    Google Scholar 

  • Ando T, Fujimoto K, Mayahara H, Miyajima H, Ogawa K (1981) A new one-step method for the histochemistry and cytochemistry of Ca2+-ATPase activity. Acta Histochem Cytochem 14:705–726

    CAS  Google Scholar 

  • Breen PC, DeBruyn PPH (1969) The fine structure of the secretory cells of the uterus (shell gland) of the chicken. J Morphol 128:35–65

    Article  PubMed  CAS  Google Scholar 

  • Cossu M, Lantini MS, Puxeddu P, Riva A (1984) Cytochemical localization of ouabain-sensitive, K+-dependent p-nitro-phenylphosphatase and Ca++-stimulated adenosine triphosphatase activities in human parotid and submandibular glands. Histochemistry 81:221–225

    Article  PubMed  CAS  Google Scholar 

  • Coty WA (1982) The hen oviduct shell gland contains high levels of calcium-stimulated ATPase activity. Fed Proc 41:463

    Google Scholar 

  • Fukushima O (1984) Mg-ATPase and Ca-ATPase activities on the plasma membrane of the metaphyseal osteoblast. Jpn J Bone Metab 2:154–162

    Google Scholar 

  • Gay CV, Schraer H (1971) Autoradiographic localization of calcium in the mucosal cells of the avian oviduct. Calcif Tissue Res 7:201–211

    Article  PubMed  CAS  Google Scholar 

  • Gay CV, Mueller WJ (1973) Cellular localization of carbonic anhydrase in avian tissues by labeled inhibitor autoradiography. J Histochem Cytochem 21:693–702

    PubMed  CAS  Google Scholar 

  • Gay CV, Faleski EJ, Schraer H, Schraer R (1974) Localization of carbonic anhydrase in avian gastric mucosa, shell gland and bone by immunohistochemistry. J Histochem Cytochem 22:819–825

    PubMed  CAS  Google Scholar 

  • Hohman W, Schraer H (1972) Low temperature ultramicroincineration of thin-sectioned tissue. J Cell Biol 55:328–354

    Article  Google Scholar 

  • Johnston HS, Aitken RNC, Wyburn GM (1963) The fine structure of the uterus of the domestic fowl. J Anat 97:333–344

    PubMed  CAS  Google Scholar 

  • Lojda Z (1965) Remarks on histochemical detection of dehydrogenases. II. Intracellular localization. Folia Morphol (Praha) 13:84–96

    CAS  Google Scholar 

  • Lojda Z, Gossrau R, Schiebler TH (1979) Enzyme histochemistry. A laboratory manual. Springer, Berlin Heidelberg New York, pp 256–296

    Google Scholar 

  • Kolaja GJ, Hinton DE (1977) In vitro inhibition of microsomal calcium ATPase from eggshell gland of mallard duck. Bull Environ Contam Toxicol 17:591–594

    Article  PubMed  CAS  Google Scholar 

  • Lippielo L, Wasserman RH (1975) Fluorescent antibody localization of the vitamin D-dependent calcium-binding protein in the oviduct of the laying hen. J Histochem Cytochem 23:111–116

    Google Scholar 

  • Lundholm CE (1982) Effect of p-p′-DDE administered in vivo and in vitro on Ca2+ binding and Ca2+−Mg2+-ATPase activity in egg shell gland mucosa of ducks. Acta Pharmacol Toxicol (Copenh) 50:121–129

    CAS  Google Scholar 

  • Miller DS, Kinter WB, Peakall DB (1976) Enzymatic basis for DDE-induced eggshell thinning in a sensitive bird. Nature 259:122–124

    Article  PubMed  CAS  Google Scholar 

  • Nachlas MM, Tsou KC, DeSouza E, Cheng CS, Seligman AM (1957) Cytochemical demonstration of succinic dehydrogenase by the use of a new p-nitrophenyl substituted ditetrazole. J Histochem Cytochem 5:420–436

    PubMed  CAS  Google Scholar 

  • Pike JW, Alvarado RH (1975) Ca2+−Mg2+-activated ATPase in the shell gland of Japanese quail (Coturnix Cotrunix Japonica). Comp Biochem Physiol 51:119–125

    Article  CAS  Google Scholar 

  • Schraer R, Schraer H (1970) The avian shell gland: A study in calcium translocation. In: Schraer H (ed) Biological calcification: Cellular and molecular aspects. Appleton, New York, pp 347–373

  • Schraer R, Elder JA, Schraer H (1973) Aspects of mitochondrial function in calcium movement and calcification. Fed Proc 32:1938–1943

    PubMed  CAS  Google Scholar 

  • Solomon SE, Fryer JR, Baird T (1975) The ultrastructural localization of calcium in the avian shell gland. J Microsc 105:215–222

    PubMed  CAS  Google Scholar 

  • Ueno M, Mizuhira V (1984) Calcium transport mechanism in crayfish gastrolith epithelium correlated with the molting cycle II. cytochemical demonstration of Ca2+-ATPase and Mg2+-ATPase. Histochemistry 80:213–217

    Article  PubMed  CAS  Google Scholar 

  • Vincenzi FF, Hinds TR (1980) Calmodulin and plasma membrane calcium transport. In: Cheung WY (ed) Calmodulin and cell function, vol 1. Academic Press, New York London, pp 127–165

    Google Scholar 

  • Woodard AE, Mather FB (1964) The timing of ovulation, movement of the ovum through the oviduct, pigmentation and shell deposition in Japanese quail (Coturnix coturnix japonica). Poult Sci 43:1427–1432

    Google Scholar 

  • Yamada M (1973) Biochemical studies on the shell gland of Japanese quail,Coturnix Coturnix Japonica I. effect of a developing egg location on activity of glycolytic and other enzymes in the shell gland. Poult Sci 52:1375–1382

    PubMed  CAS  Google Scholar 

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Yamamoto, T., Ozawa, H. & Nagai, H. Histochemical studies of Ca-ATPase, succinate and NAD+-dependent isocitrate dehydrogenases in the shell gland of laying Japanese quails: with special reference to calcium-transporting cells. Histochemistry 83, 221–226 (1985). https://doi.org/10.1007/BF00953987

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  • DOI: https://doi.org/10.1007/BF00953987

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