Adipokine gene transcription level in adipose tissue of runt piglets

Comparative Biochemistry and Physiology - B Biochemistry and Molecular Biology

Volumn 155, Issue 2, 2010, Pages 97-105

  Ramsay, T G ^a   Stoll, M J ^a   Caperna, T J ^a  

^a AGRICULTURAL RESEARCH SERVICE   (United States)

Author keywords

Adipokine; Adipose tissue; Cytokine; Neonate; Runt

Indexed keywords

ADIPOCYTOKINE; ADIPONECTIN; INTERLEUKIN 10; INTERLEUKIN 15; INTERLEUKIN 1BETA; INTERLEUKIN 6; INTERLEUKIN 8; LEPTIN; MESSENGER RNA;

ADIPOSE TISSUE; AMPLICON; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; FEMALE; GENETIC TRANSCRIPTION; MALE; NEONATAL STRESS; NONHUMAN; NUCLEOTIDE SEQUENCE; PIGLET; PRIORITY JOURNAL; REAL TIME POLYMERASE CHAIN REACTION; REVERSE TRANSCRIPTION; RNA ANALYSIS; RNA ISOLATION;

EID: 72149086118     PISSN: 10964959     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbpb.2009.09.006     Document Type: Article

References (57)

1. Anderson D.B., Kauffman R.G., and Kastenschmidt L.L. Lipogenic enzyme activities and cellularity of porcine adipose tissue from various anatomical locations. J. Lipid Res. 13 (1972) 593-599
2. Anderson D.B., and Kauffman R.G. Cellular and enzymatic changes in porcine adipose tissue during growth. J. Lipid Res. 14 (1973) 160-168
3. Atsumi T., Cho Y.R., Leng L., McDonald C., Yu T., Danton C., Hong E.G., Mitchell R.A., Metz C., Niwa H., Takeuchi J., Onodera S., Umino T., Yoshioka N., Koike T., Kim J.K., and Bucala R. The proinflammatory cytokine macrophage migration inhibitory factor regulates glucose metabolism during systemic inflammation. J. Immunol. 179 (2007) 5399-5406
4. Brix-Christensen V., Vestergaard C., Andersen S.K., Krog J., Andersen N.T., Larsson A., Schmitz O., and Tonnesen E. Evidence that acute hyperinsulinaemia increases the cytokine content in essential organs after an endotoxin challenge in a porcine model. Acta Anaesthesiol. Scand. 49 (2005) 1429-1435
5. Bruun J.M., Pedersen S.B., Kristensen K., and Richelsen B. Effects of pro-inflammatory cytokines and chemokines on leptin production in human adipose tissue in vitro. Mol. Cell. Endocrinol. 190 (2002) 91-99
6. Budd T.J., Atkinson J.L., Buttery P.J., Salter A.M., and Wiseman J. Effect of insulin and isoproterenol on lipid metabolism in porcine adipose tissue from different depots. Comp. Biochem. Physiol. Pharmacol. Toxicol. Endocrinol. 108 (1994) 137-143
7. Chen X., Hausman D.B., Dean R.G., and Hausman G.J. Differentiation-dependent expression of obese (ob) gene by preadipocytes and adipocytes in primary cultures of porcine stromal-vascular cells. Biochem. Biophys. Acta 1359 (1997) 136-142
8. Choi I.S., Collisson E.W., Maheswaran S.K., and Yoo H.S. Evaluation of cytokine gene expression in porcine spleen cells, peripheral blood mononuclear cells, and alveolar macrophages by competitive RT-PCR. FEMS Immunol. Med. Microbiol. 34 (2002) 119-126
9. Cianfarani S., Martinez C., Maiorana A., Scire` G., Spadoni G.L., and Boemi S. Adiponectin levels are reduced in children born small for gestational age and are inversely related to postnatal catch-up growth. J. Clin. Endocrinol. Metab. 89 (2004) 1346-1351
10. Curtis S.E. Responses of the piglet to perinatal stressors. J. Anim. Sci. 38 (1974) 1031-1036
11. Fain J.N. Release of interleukins and other inflammatory cytokines by human adipose tissue is enhanced in obesity and primarily due to the nonfat cells. Vitam. Horm. 74 (2006) 443-477
12. Flaster H., Bernhagen J., Calandra T., and Bucala R. The macrophage migration inhibitory factor-glucocorticoid dyad: regulation of inflammation and immunity. Mol. Endocrinol. 21 (2007) 1267-1280
13. Flower L., Gray R., Pinkney J., and Mohamed-Ali V. Stimulation of interleukin-6 release by interleukin-1beta from isolated human adipocytes. Cytokine 21 (2003) 32-37
14. Gardan D., Gondret F., and Louveau I. Lipid metabolism and secretory function of porcine intramuscular adipocytes compared with subcutaneous and perirenal adipocytes. Am. J. Physiol. Endocrinol. Metab. 291 (2006) E372-380
15. Greenberg A.S., Nordan R.P., McIntosh J., Calvo J.C., Scow R.O., and Jablons D. Interleukin 6 reduces lipoprotein lipase activity in adipose tissue of mice in vivo and in 3T3-L1 adipocytes: a possible role for interleukin 6 in cancer cachexia. Cancer Res. 52 (1992) 4113-4116
16. Hausman G.J., and Kauffman R.G. The histology of developing porcine adipose tissue. J. Anim. Sci. 63 (1986) 642-658
17. Hausman G.J., Poulos S.P., Richardson R.L., Barb C.R., Andacht T., Kirk H.C., and Mynatt R.L. Secreted proteins and genes in fetal and neonatal pig adipose tissue and stromal-vascular cells. J. Anim. Sci. 84 (2006) 1666-1681
18. Hegarty P.V., and Allen C.E. Effect of pre-natal runting on the post-natal development of skeletal muscles in swine and rats. J. Anim. Sci. 46 (1978) 1634-1640
19. Hentges E.J., and Hausman G.J. Primary cultures of stromal-vascular cells from pig adipose tissue: the influence of glucocorticoids and insulin as inducers of adipocyte differentiation. Domest. Anim. Endocrinol. 6 (1989) 275-285
20. Hirokawa J., Sakaue S., Furuya Y., Ishii J., Hasegawa A., Tagami S., Kawakami Y., Sakai M., Nishi S., and Nishihira J. Tumor necrosis factor-alpha regulates the gene expression of macrophage migration inhibitory factor through tyrosine kinase-dependent pathway in 3T3-L1 adipocytes. J. Biochem. 123 (1998) 733-739
21. Hoi A.Y., Iskander M.N., and Morand E.F. Macrophage migration inhibitory factor: a therapeutic target across inflammatory diseases. Inflamm. Allergy Drug Targets 6 (2007) 183-190
22. Jaquet D., Leger J., Levy-Marchal C., Oury J.F., and Czernichow P. Ontogeny of leptin in human fetuses and newborns: effect of intrauterine growth retardation on serum leptin concentrations. J. Clin. Endocrinol. Metab. 83 (1998) 1243-1246
23. Kamoda T., Saitoh H., Saito M., Sugiura M., and Matsui A. Serum adiponectin concentrations in newborn infants in early postnatal life. Pediatr. Res. 56 (2004) 690-693
24. Lagathu C., Yvan-Charvet L., Bastard J.P., Maachi M., Quignard-Boulange A., Capeau J., and Caron M. Long-term treatment with interleukin-1beta induces insulin resistance in murine and human adipocytes. Diabetologia 49 (2006) 2162-2173
25. Laws J., Litten J.C., Laws A., Lean I.J., Dodds P.F., and Clarke L. Effect of type and timing of oil supplements to sows during pregnancy on the growth performance and endocrine profile of low and normal birth weight offspring. Br. J. Nutr (2008) 10.1017/S0007114508998469 S0007114508998469 [pii]
26. Lay Jr. D.C., Haussmann M.F., Buchanan H.S., and Daniels M.J. Danger to pigs due to crushing can be reduced by the use of a simulated udder. J. Anim. Sci. 77 (1999) 2060-2064
27. Livak K.J., and Schmittgen T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 25 (2001) 402-408
28. McNeel R.L., Ding S.T., Smith E.O., and Mersmann H.J. Effect of feed restriction on adipose tissue transcript concentrations in genetically lean and obese pigs. J. Anim. Sci. 78 (2000) 934-942
29. Mersmann H.J. Metabolic patterns in the neonatal swine. J. Anim. Sci. 38 (1974) 1022-1030
30. Mersmann H.J., Goodman J.R., and Brown L.J. Development of swine adipose tissue: morphology and chemical composition. J. Lipid Res. 16 (1975) 269-279
31. Morise A., Seve B., Mace K., Magliola C., Le Huerou-Luron I., and Louveau I. Impact of intrauterine growth retardation and early protein intake on growth, adipose tissue and the IGF system in piglets. Pediatr. Res. 65 (2009) 45-50
32. O'Reilly K.M., Harris M.J., Mendl M., Held S., Moinard C., Statham P., Marchant-Forde J., and Green L.E. Factors associated with preweaning mortality on commercial pig farms in England and Wales. Vet. Rec. 159 (2006) 193-196
33. Petersen E.W., Carey A.L., Sacchetti M., Steinberg G.R., Macaulay S.L., Febbraio M.A., and Pedersen B.K. Acute IL-6 treatment increases fatty acid turnover in elderly humans in vivo and in tissue culture in vitro. Am. J. Physiol. Endocrinol. Metab. 288 (2005) E155-162
34. Price S.R., Olivecrona T., and Pekala P.H. Regulation of lipoprotein lipase synthesis by recombinant tumor necrosis factor-the primary regulatory role of the hormone in 3T3-L1 adipocytes. Arch. Biochem. Biophys. 251 (1986) 738-746
35. Quiniou N., Dagorn J., and Gaudre D. Variation of piglets' birth weight and consequences on subsequent performance. Livestock Prod. Sci. 78 (2002) 63-70
36. Ramsay T.G., and Caperna T.J. Ontogeny of adipokine expression in neonatal pig adipose tissue. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 152 (2009) 72-78
37. Ramsay T.G., White M.E., and Wolverton C.K. Glucocorticoids and the differentiation of porcine preadipocytes. J. Anim. Sci. 67 (1989) 2222-2229
38. Ramsay T.G., Mitchell A.D., and Richards M.P. Uncoupling protein expression in skeletal muscle and adipose tissue in response to in vivo porcine somatotropin treatment. Domest. Anim. Endocrinol. 35 (2008) 130-141
39. Randall G.C. Observations on parturition in the sow. II. Factors influencing stillbirth and perinatal mortality. Vet. Rec. 90 (1972) 183-186
40. Rehfeldt C., and Kuhn G. Consequences of birth weight for postnatal growth performance and carcass quality in pigs as related to myogenesis. J. Anim. Sci. 84 (2006) E113-123 Suppl
41. Rotter V., Nagaev I., and Smith U. Interleukin-6 (IL-6) induces insulin resistance in 3T3-L1 adipocytes and is, like IL-8 and tumor necrosis factor-alpha, overexpressed in human fat cells from insulin-resistant subjects. J. Biol. Chem. 278 (2003) 45,777-45,784
42. Ruan H., and Lodish H.F. Insulin resistance in adipose tissue: direct and indirect effects of tumor necrosis factor-alpha. Cytokine Growth Factor Rev. 14 (2003) 447-455
43. Sakaue S., Nishihira J., Hirokawa J., Yoshimura H., Honda T., Aoki K., Tagami S., and Kawakami Y. Regulation of macrophage migration inhibitory factor (MIF) expression by glucose and insulin in adipocytes in vitro. Mol. Med. 5 (1999) 361-371
44. Samulin J., Lien S., Grindflek E., Berget I., Ruyter B., and Sundvold H.m. Depot specific differences during adipogenesis of porcine stromal-vascular cells. Cell Biol. Int. 32 (2008) 525-531
45. Schultz C., Temming P., Bucsky P., Gopel W., Strunk T., and Hartel C. Immature anti-inflammatory response in neonates. Clin. Exp. Immunol. 135 (2004) 130-136
46. Senn J.J., Klover P.J., Nowak I.A., Zimmers T.A., Koniaris L.G., Furlanetto R.W., and Mooney R.A. Suppressor of cytokine signaling-3 (SOCS-3), a potential mediator of interleukin-6-dependent insulin resistance in hepatocytes. J. Biol. Chem. 278 (2003) 13,740-13,746
47. Stanton H.C., and Carroll J.K. Potential mechanisms responsible for prenatal and perinatal mortality or low viability of swine. J. Anim. Sci. 38 (1974) 1037-1044
48. Suryawan A., Swanson L.V., and Hu C.Y. Insulin and hydrocortisone, but not triiodothyronine, are required for the differentiation of pig preadipocytes in primary culture. J. Anim. Sci. 75 (1997) 105-111
49. Tilg H., and Moschen A.R. Adipocytokines: mediators linking adipose tissue, inflammation and immunity. Nat. Rev. Immunol. 6 (2006) 772-783
50. Toso C., Emamaullee J.A., Merani S., and Shapiro A.M. The role of macrophage migration inhibitory factor on glucose metabolism and diabetes. Diabetologia 51 (2008) 1937-1946 10.1007/s00125-008-1063-3
51. Trayhurn P., and Wood I.S. Signalling role of adipose tissue: adipokines and inflammation in obesity. Biochem. Soc. Trans. 33 (2005) 1078-1081
52. Trujillo M.E., Sullivan S., Harten I., Schneider S.H., Greenberg A.S., and Fried S.K. Interleukin-6 regulates human adipose tissue lipid metabolism and leptin production in vitro. J. Clin. Endocrinol. Metab. 89 (2004) 5577-5582
53. Tsigos C., Papanicolaou D.A., Kyrou I., Defensor R., Mitsiadis C.S., and Chrousos G.P. Dose-dependent effects of recombinant human interleukin-6 on glucose regulation. J. Clin. Endocrinol. Metab. 82 (1997) 4167-4170
54. Tuchscherer M., Puppe B., Tuchscherer A., and Tiemann U. Early identification of neonates at risk: traits of newborn piglets with respect to survival. Theriogenology 54 (2000) 371-388
55. Wang B., and Trayhurn P. Acute and prolonged effects of TNF-alpha on the expression and secretion of inflammation-related adipokines by human adipocytes differentiated in culture. Pflugers Arch. 452 (2006) 418-427
56. Winer J., Jung C.K., Shackel I., and Williams P.M. Development and validation of real-time quantitative reverse transcriptase-polymerase chain reaction for monitoring gene expression in cardiac myocytes in vitro. Anal. Biochem. 270 (1999) 41-49
57. Wu J., Cunha F.Q., Liew F.Y., and Weiser W.Y. IL-10 inhibits the synthesis of migration inhibitory factor and migration inhibitory factor-mediated macrophage activation. J. Immunol. 151 (1993) 4325-4332