Dynamic expression of TRPV6, cal bind in D28k and PMCA 1b in the egg during the oviposition cycle in laying hens

International Journal of Agriculture & Environmental Science
© 2017 by SSRG - IJAES Journal
Volume 4 Issue 5
Year of Publication : 2017
Authors : Xiaohu Zhai, Weihua HE, Jiafa HOU, Junhua YANG
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Xiaohu Zhai, Weihua HE, Jiafa HOU, Junhua YANG, "Dynamic expression of TRPV6, cal bind in D28k and PMCA 1b in the egg during the oviposition cycle in laying hens," SSRG International Journal of Agriculture & Environmental Science, vol. 4,  no. 5, pp. 4-12, 2017. Crossref, https://doi.org/10.14445/23942568/IJAES-V4I5P102

Abstract:

The aim of this study is to investigate the effect of active Ca2+ transcellular transport on the eggshell calcification. Forty ISA laying hens at the peak stage (220 days old) were assigned to five reproductive stages for sampling. The samples of eggshell gland (ESG) were obtained by the chickens were sacrificed at 0, 2, 4.5, 8 and 16 h after post-oviposition, respectively. Then, quantization’s of mRNA level and protein concentration of TRPV6, CaBP-D28K and PMCA 1b at different stages in the ESG were carried out by real-time PCR and western-blot analysis, respectively. The results are as follows: the expression levels of TRPV6, CaBP-D28K and PMCA 1b mRNA in the ESG were retained very low until the egg movement into the shell gland (0~4.5 h after ovulation), then significantly increased at 16 h during eggshell calcification. In addition, TRPV6, and CaBP-D28K indicated significant statistical difference (P<0.01), respectively. Furthermore, western blotting showed that the expression of TRPV6 and PMCA 1b reached the maximum at 16 h after ovulation, but the statistical difference was not significant. The change of CaBP-D28K expression was very similar to that of TRPV6, but the concentration was significantly increased at 16 h than that at 0 h after ovulation (P<0.05). In conclusion, the expression of TRPV6, CaBP-D28K and PMCA 1b in the ESG was regulated by the oviposition cycle, suggesting that active Ca2+ transcellular transport exerted significant effects in calcium delivering in the ESG.

Keywords:

ESG; TRPV6; CaBP-D28K; PMCA 1b; the oviposition cycle

References:

[1] Eastin W C, Spaziani E. On the control of calcium secretion in the avian shell gland (uterus) [J]. Biol Reprod, 1978, 19(3): 493-504.
[2] Eastin W C, Spaziani E. On the mechanism of calcium secretion in the avian shell gland (uterus) [J]. Biol Reprod, 1978, 19(3): 505-518.
[3] Cohen I, Hurwitz S. Intracellular pH and electrolyte concentration in the uterine wall of the fowl in relation to shell formation and dietary minerals [J]. Comp Biochem Physiol Part-A Physiol, 1974, 49(4): 689-696.
[4] Hurwitz S, Cohen I, Bar A. The transmembrane electrical potential difference in the uterus (shell gland) of birds [J]. Comp Biochem Physiol, 1970, 35(4): 873-878.
[5] Pearson T, Goldner A. Calcium transport across avian uterus. I. Effects of electrolyte substitution [J]. Am J Physiol, 1973, 225(6): 1508-1512.
[6] Bar A. Calcium transport in strongly calcifying laying birds: mechanisms and regulation [J]. Comp Biochem Physiol Part-A Mol Integr Physiol, 2009, 152(4): 447-469.
[7] Schraer H, Schraer R. Calcium transfer across the avian shell gland [M].New York, 1971.
[8] Corradino R, Wasserman R, Pubols M, et al. Vitamin D3 induction of a calcium-binding protein in the uterus of the laying hen [J]. Arch Biochem Biophys, 1968, 125(1): 378-380.
[9] Wasserman R H, Smith C A, Smith C M, et al. Immunohistochemical localization of a calcium pump and calbindin-D28k in the oviduct of the laying hen [J]. Histochemistry, 1991, 96(5): 413-418.
[10] Wesley Pike J, Alvarado R H. Ca2+--Mg2+-activated ATPase in the shell gland of Japanese quail (Coturnix coturnix Japonica) [J]. Comp Biochem Physiol Part B: Comp Biochem, 1975, 51(1): 119-125.
[11] Borke J L, Caride A, Verma A K, et al. Plasma membrane calcium pump and 28-kDa calcium binding protein in cells of rat kidney distal tubules [J]. Am J Physiol Renal Physiol, 1989, 257(5): F842-849.
[12] Borke J L, Caride A, Verma A K, et al. Cellular and segmental distribution of Ca2+-pump epitopes in rat intestine [J]. Pflügers Arch Eur J Physiol, 1990, 417(1): 120-122.
[13] Hu Y, Ni Y, Ren L, et al. Leptin is involved in the effects of cysteamine on egg laying of hens, characteristics of eggs, and posthatch growth of broiler offspring [J]. Poult Sci, 2008, 87(9): 1810-1817.
[14] Livak K J, Schmittgen T D. Analysis of relative gene expression data using Real-time quantitative PCR and the 2-[Delta][Delta]CT method [J]. Methods, 2001, 25(4): 402-408.
[15] Bianco S D, Peng J B, Takanaga H, et al. Marked disturbance of calcium homeostasis in mice with targeted disruption of the Trpv6 calcium channel gene [J]. J Bone Miner Res, 2007, 22(2): 274-285.
[16] Choi Y, Seo H, Kim M, et al. Dynamic expression of calcium-regulatory molecules, TRPV6 and S100G, in the uterine endometrium during pregnancy in pigs [J]. Biol Reprod, 2009, 81(6): 1122-1130.
[17] Lee G S, Jeung E B. Uterine TRPV6 expression during the estrous cycle and pregnancy in a mouse model [J]. Am J Physiol Endocrinol Metab, 2007, 293(1): E132-138.
[18] Taylor A N, Wasserman R H. Vitamin D3-induced calcium-binding protein: Partial purification, electrophoretic visualization, and tissue distribution [J]. Arch Biochem Biophys, 1967, 119:536-540.
[19] Christakos S, Liu Y, Dhawan P, et al. The calbindins: Calbindin-D9K and calbindin-D28K. [M]. London: Elsevier Academic Press, Burlington, MA; San Diego, CA, 2005.
[20] Lambers T T, Mahieu F, Oancea E, et al. Calbindin-D28K dynamically controls TRPV5-mediated Ca2+ transport [J]. Embo J, 2006, 25(13): 2978-2988.
[21] Christakos S, Barletta F, Huening M, et al. Vitamin D target proteins: function and regulation [J]. J Cell Biochem, 2003, 88(2): 238-244.
[22] Christakos S, Dhawan P, Benn B, et al. Vitamin D: molecular mechanism of action [J]. Ann NY Acad Sci, 2007, 1116:340-348.
[23] Lippiello L, Wasserman R. Fluorescent antibody localization of the vitamin D-dependent calcium-binding protein in the oviduct of the laying hen [J]. J Histochem Cytochem, 1975, 23(2): 111-116.
[24] Jande S S, Tolnai S, Lawson D E. Immunohistochemical localization of vitamin D-dependent calcium-binding protein in duodenum, kidney, uterus and cerebellum of chickens [J]. Histochemistry, 1981, 71(1): 99-116.
[25] Nys Y, Mayel-Afshar S, Bouillon R, et al. Increases in calbindin D 28K mRNA in the uterus of the domestic fowl induced by sexual maturity and shell formation [J]. Gen Comp Endocrinol, 1989, 76(2): 322-329.
[26] Bar A, Striem S, Vax E, et al. Regulation of calbindin mRNA and calbindin turnover in intestine and shell gland of the chicken [J]. Am J Physiol Regul Integr Comp Physiol, 1992, 262(5): R800-805.
[27] Bar A, Vax E, Striem S. Relationships between calbindin (Mr 28,000) and calcium transport by the eggshell gland [J]. Comp Biochem and Physiol Part A: Physiol, 1992, 101(4): 845-848.
[28] Nys Y, Baker K, Lawson D E. Estrogen and a calcium flux dependent factor modulate the calbindin gene expression in the uterus of laying hens [J]. Gen Comp Endocrinol, 1992, 87(1): 87-94.
[29] Ieda T, Saito N, Ono T, et al. Effects of presence of an egg and calcium deposition in the shell gland on levels of messenger ribonucleic acid of CaBP-D28K and of Vitamin D3 receptor in the shell gland of the laying hen [J]. Gen Comp Endocrinol, 1995, 99(2): 145-151.
[30] Borke J L, Caride A, Verma A K, et al. Calcium pump epitopes in placental trophoblast basal plasma membranes [J]. Am J Physiol Cell Physiol, 1989, 257(2): C341-346.