Expression of transcripts related to intestinal ion and nutrient absorption in pregnant and lactating rats as determined by custom-designed cDNA microarray

Molecular and Cellular Biochemistry

Volumn 391, Issue 1-2, 2014, Pages 103-116

  Teerapornpuntakit, Jarinthorn ^a   Klanchui, Amornpan ^b   Karoonuthaisiri, Nitsara ^b   Wongdee, Kannikar ^a,c   Charoenphandhu, Narattaphol ^a  

^a Mahidol University ^*  (Thailand)

^b NATIONAL SCIENCE AND TECHNOLOGY DEVELOPMENT AGENCY   (Thailand)

^c BURAPHA UNIVERSITY   (Thailand)

Author keywords

Bromocriptine; Calcium absorption; Custom designed cDNA microarray; Nutrient absorption; Prolactin

Indexed keywords

BROMOCRIPTINE; CALCIUM; CLDN19 PROTEIN; COMPLEMENTARY DNA; CYP27B1 PROTEIN; FGFR2C PROTEIN; GLUCOSE TRANSPORTER 1; INSULIN; INSULIN 2; INTESTINAL ION; ION; MESSENGER RNA; PROLACTIN; PROTEIN; SOLUTE CARRIER ORGANIC ANION TRANSPORTER 1B2; TRANSCRIPTOME; UNCLASSIFIED DRUG; DNA PROBE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BONE METABOLISM; CALCIUM BONE LEVEL; CALCIUM METABOLISM; CELL METABOLISM; COMPARATIVE STUDY; CONTROLLED STUDY; DNA MICROARRAY; FEMALE; GENE EXPRESSION; GENETIC TRANSCRIPTION; INTESTINE ABSORPTION; INTESTINE EPITHELIUM CELL; ION TRANSPORT; LACTATION; NONHUMAN; NUTRIENT; OLIGONUCLEOTIDE PROBE; PARACRINE SIGNALING; PREGNANCY; PROLACTIN RELEASE; RAT; REAL TIME POLYMERASE CHAIN REACTION; SMALL INTESTINE; UPREGULATION; ANIMAL; COMPUTER PROGRAM; DNA PROBE; DUODENUM; ESSENTIAL GENE; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; PROCEDURES; REPRODUCIBILITY; SPRAGUE DAWLEY RAT;

RATTUS;

ANIMALS; DNA PROBES; DUODENUM; FEMALE; GENE EXPRESSION REGULATION; GENES, ESSENTIAL; INTESTINAL ABSORPTION; IONS; LACTATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PREGNANCY; RATS, SPRAGUE-DAWLEY; REAL-TIME POLYMERASE CHAIN REACTION; REPRODUCIBILITY OF RESULTS; RNA, MESSENGER; SOFTWARE;

EID: 84900826318     PISSN: 03008177     EISSN: 15734919     Source Type: Journal    
DOI: 10.1007/s11010-014-1992-8     Document Type: Article

References (61)

1. Cripps AW, Williams VJ (1975) The effect of pregnancy and lactation on food intake, gastrointestinal anatomy and the absorptive capacity of the small intestine in the albino rat. Br J Nutr 33:17-32
2. Mainoya JR (1975) Influence of reproductive state on intestinal fluid and ion transport by the rat jejunum, in relation to the possible contribution of prolactin. J Endocrinol 67:351-358
3. Larralde J, Fernandez-Otero P, Gonzalez M (1966) Increased active transport of glucose through the intestine during pregnancy. Nature 209:1356-1357
4. 2+ absorption during lactation by long-term prolactin exposure and suckling-induced prolactin surge. Am J Physiol Endocrinol Metab 297:E609-E619
5. Fell BF, Smith KA, Campbell RM (1963) Hypertrophic and hyperplastic changes in the alimentary canal of the lactating rat. J Pathol Bacteriol 85:179-188
6. Soares MJ, Konno T, Alam SM (2007) The prolactin family: effectors of pregnancy-dependent adaptations. Trends Endocrinol Metab 18:114-121
7. Charoenphandhu N, Wongdee K, Krishnamra N (2010) Is prolactin the cardinal calciotropic maternal hormone? Trends Endocrinol Metab 21:395-401
8. Charoenphandhu N, Krishnamra N (2007) Prolactin is an important regulator of intestinal calcium transport. Can J Physiol Pharmacol 85:569-581
9. Teerapornpuntakit J, Wongdee K, Thongbunchoo J, Krishnamra N, Charoenphandhu N (2012) Proliferation and mRNA expression of absorptive villous cell markers and mineral transporters in prolactin-exposed IEC-6 intestinal crypt cells. Cell Biochem Funct 30:320-327
10. Ramsey DH, Bern HA (1972) Stimulation by ovine prolactin of fluid transfer in everted sacs of rat small intestine. J Endocrinol 53:453-459
11. Mainoya JR (1975) Effect of prolactin on sugar and amino acid transport by the rat jejunum. J Exp Zool 192:149-154
12. Oakes SR, Rogers RL, Naylor MJ, Ormandy CJ (2008) Prolactin regulation of mammary gland development. J Mammary Gland Biol Neoplasia 13:13-28
13. Wongdee K, Charoenphandhu N (2013) Regulation of epithelial calcium transport by prolactin: from fish to mammals. Gen Comp Endocrinol 181:235-240
14. Holmes JL, Van Itallie CM, Rasmussen JE, Anderson JM (2006) Claudin profiling in the mouse during postnatal intestinal development and along the gastrointestinal tract reveals complex expression patterns. Gene Expr Patterns 6:581-588
15. Anderson JM, Van Itallie CM (2009) Physiology and function of the tight junction. Cold Spring Harb Perspect Biol 1:a002584. doi:10.1101/cshperspect. a002584
16. Kraus P, Xing X, Lim SL, Fun ME, Sivakamasundari V, Yap SP, Lee H, Karuturi RK, Lufkin T (2012) Mouse strain specific gene expression differences for illumina microarray expression profiling in embryos. BMC Res Notes 5:232. doi:10.1186/1756-0500-5-232
17. Charoenphandhu N, Wongdee K, Teerapornpuntakit J, Thongchote K, Krishnamra N (2008) Transcriptome responses of duodenal epithelial cells to prolactin in pituitary-grafted rats. Mol Cell Endocrinol 296:41-52
18. Teerapornpuntakit J, Dorkkam N, Wongdee K, Krishnamra N, Charoenphandhu N (2009) Endurance swimming stimulates transepithelial calcium transport and alters the expression of genes related to calcium absorption in the intestine of rats. Am J Physiol Endocrinol Metab 296:E775-E786
19. Jantarajit W, Thongon N, Pandaranandaka J, Teerapornpuntakit J, Krishnamra N, Charoenphandhu N (2007) Prolactin-stimulated transepithelial calcium transport in duodenum and Caco-2 monolayer are mediated by the phosphoinositide 3-kinase pathway. Am J Physiol Endocrinol Metab 293:E372-E384
20. Leelatanawit R, Uawisetwathana U, Klinbunga S, Karoonuthaisiri N (2011) A cDNA microarray, UniShrimpChip, for identification of genes relevant to testicular development in the black tiger shrimp (Penaeus monodon). BMC Mol Biol 12:15. doi:10.1186/1471-2199-12-15
21. Karoonuthaisiri N, Sittikankeaw K, Preechaphol R, Kalachikov S, Wongsurawat T, Uawisetwathana U, Russo JJ, Ju J, Klinbunga S, Kirtikara K (2009) ReproArray (GTS): a cDNA microarray for identification of reproduction-related genes in the giant tiger shrimp Penaeus monodon and characterization of a novel nuclear autoantigenic sperm protein (NASP) gene. Comp Biochem Physiol D 4:90-99
22. Uawisetwathana U, Leelatanawit R, Klanchui A, Prommoon J, Klinbunga S, Karoonuthaisiri N (2011) Insights into eyestalk ablation mechanism to induce ovarian maturation in the black tiger shrimp. PLoS ONE 6:e24427. doi:10.1371/journal.pone.0024427
23. Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A, Speleman F (2002) Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol 3:research0034. doi:10.1186/gb-2002-3-7-research0034
24. Andersen CL, Jensen JL, Orntoft TF (2004) Normalization of real-time quantitative reverse transcription-PCR data: a model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets. Cancer Res 64:5245-5250
25. Rungrassamee W, Tosukhowong A, Klanchui A, Maibunkaew S, Plengvidhya V, Karoonuthaisiri N (2012) Development of bacteria identification array to detect lactobacilli in Thai fermented sausage. J Microbiol Methods 91:341-353
26. Eisen MB, Spellman PT, Brown PO, Botstein D (1998) Cluster analysis and display of genome-wide expression patterns. Proc Natl Acad Sci USA 95:14863-14868
27. -ΔΔCt method. Methods 25:402-408
28. Buehlmeyer K, Doering F, Daniel H, Schulz T, Michna H (2007) Exercise associated genes in rat colon mucosa: upregulation of ornithin decarboxylase-1. Int J Sports Med 28:361-367
29. Yamada H, Chen D, Monstein HJ, Hakanson R (1997) Effects of fasting on the expression of gastrin, cholecystokinin, and somatostatin genes and of various housekeeping genes in the pancreas and upper digestive tract of rats. Biochem Biophys Res Commun 231:835-838
30. Li B, Matter EK, Hoppert HT, Grayson BE, Seeley RJ, Sandoval DA (2013) Identification of optimal reference genes for RT-qPCR in the rat hypothalamus and intestine for the study of obesity. Int J Obes (Lond). doi:10.1038/ijo.2013. 86
31. Martinez-Beamonte R, Navarro MA, Larraga A, Strunk M, Barranquero C, Acin S, Guzman MA, Inigo P, Osada J (2011) Selection of reference genes for gene expression studies in rats. J Biotechnol 151:325-334
32. Hammond KA (1997) Adaptation of the maternal intestine during lactation. J Mammary Gland Biol Neoplasia 2:243-252
33. Musacchia XJ, Hartner AM (1970) Intestinal absorption of glucose, and blood glucose and hematocrit in pregnant and non-pregnant hamsters. Proc Soc Exp Biol Med 135:307-310
34. Davies NT, Williams RB (1977) The effect of pregnancy and lactation on the absorption of zinc and lysine by the rat duodenum in situ. Br J Nutr 38:417-423
35. Barrett JF, Whittaker PG, Williams JG, Lind T (1994) Absorption of non-haem iron from food during normal pregnancy. Br Med J 309:79-82
36. Fung EB, Ritchie LD, Woodhouse LR, Roehl R, King JC (1997) Zinc absorption in women during pregnancy and lactation: a longitudinal study. Am J Clin Nutr 66:80-88
37. Hoenderop JG, Nilius B, Bindels RJ (2005) Calcium absorption across epithelia. Physiol Rev 85:373-422
38. 2+ absorption between enterocytes. Mol Biol Cell 19:1912-1921
39. + pumps during establishment of epithelial monolayers. Am J Physiol 257:C896-C905
40. Tanrattana C, Charoenphandhu N, Limlomwongse L, Krishnamra N (2004) Prolactin directly stimulated the solvent drag-induced calcium transport in the duodenum of female rats. Biochim Biophys Acta 1665:81-91
41. Koeppen BM, Stanton BA (2008) Homeostasis of body fluids. In: Koeppen BM, Stanton BA (eds) Berne & Levy physiology, 6th edn. Mosby-Elsevier, Philadelphia, pp 20-33
42. Pappenheimer JR, Reiss KZ (1987) Contribution of solvent drag through intercellular junctions to absorption of nutrients by the small intestine of the rat. J Membr Biol 100:123-136
43. Larsen EH, Nedergaard S, Ussing HH (2000) Role of lateral intercellular space and sodium recirculation for isotonic transport in leaky epithelia. Rev Physiol Biochem Pharmacol 141:153-212
44. Burdett K, Reek C (1979) Adaptation of the small intestine during pregnancy and lactation in the rat. Biochem J 184:245-251
45. Wikvall K (2001) Cytochrome P450 enzymes in the bioactivation of vitamin D to its hormonal form. Int J Mol Med 7:201-209
46. Marks J, Debnam ES, Unwin RJ (2010) Phosphate homeostasis and the renal-gastrointestinal axis. Am J Physiol Renal Physiol 299:F285-F296
47. Balesaria S, Sangha S, Walters JR (2009) Human duodenum responses to vitamin D metabolites of TRPV6 and other genes involved in calcium absorption. Am J Physiol Gastrointest Liver Physiol 297:G1193-G1197
48. Spanos E, Colston KW, Evans IM, Galante LS, Macauley SJ, Macintyre I (1976) Effect of prolactin on vitamin D metabolism. Mol Cell Endocrinol 5:163-167
49. 3 1α hydroxylase gene by prolactin. Endocrinology 151:2974-2984
50. Paravicini TM, Chubanov V, Gudermann T (2012) TRPM7: a unique channel involved in magnesium homeostasis. Int J Biochem Cell Biol 44:1381-1384
51. Clark K, Langeslag M, van Leeuwen B, Ran L, Ryazanov AG, Figdor CG, Moolenaar WH, Jalink K, van Leeuwen FN (2006) TRPM7, a novel regulator of actomyosin contractility and cell adhesion. EMBO J 25:290-301
52. 2+ homeostasis. Science 322:756-760
53. +-ATPase in epithelia depends on the association between β-subunits located in neighboring cells. Mol Biol Cell 16:1071-1081
54. Cancilla B, Ford-Perriss MD, Bertram JF (1999) Expression and localization of fibroblast growth factors and fibroblast growth factor receptors in the developing rat kidney. Kidney Int 56:2025-2039
55. Poole TJ, Finkelstein EB, Cox CM (2001) The role of FGF and VEGF in angioblast induction and migration during vascular development. Dev Dyn 220:1-17
56. Cui Y, Li Q (2008) Effect of mammogenic hormones on the expression of FGF7, FGF10 and their receptor in mouse mammary gland. Sci China C Life Sci 51:711-717
57. Miyamoto T, Morita K, Takemoto D, Takeuchi K, Kitano Y, Miyakawa T, Nakayama K, Okamura Y, Sasaki H, Miyachi Y, Furuse M, Tsukita S (2005) Tight junctions in Schwann cells of peripheral myelinated axons: a lesson from claudin-19-deficient mice. J Cell Biol 169:527-538
58. Konrad M, Schaller A, Seelow D, Pandey AV, Waldegger S, Lesslauer A, Vitzthum H, Suzuki Y, Luk JM, Becker C, Schlingmann KP, Schmid M, Rodriguez-Soriano J, Ariceta G, Cano F, Enriquez R, Jüppner H, Bakkaloglu SA, Hediger MA, Gallati S, Neuhauss SC, Nürnberg P, Weber S (2006) Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement. Am J Hum Genet 79:949-957
59. Angelow S, El-Husseini R, Kanzawa SA, Yu AS (2007) Renal localization and function of the tight junction protein, claudin-19. Am J Physiol Renal Physiol 293:F166-F177
60. Charoenphandhu N, Wongdee K, Tudpor K, Pandaranandaka J, Krishnamra N (2007) Chronic metabolic acidosis upregulated claudin mRNA expression in the duodenal enterocytes of female rats. Life Sci 80:1729-1737
61. Naeem M, Hussain S, Akhtar N (2011) Mutation in the tight-junction gene claudin 19 (CLDN19) and familial hypomagnesemia, hypercalciuria, nephrocalcinosis (FHHNC) and severe ocular disease. Am J Nephrol 34:241-248