Maternal Nutrient Restriction Upregulates Growth Signaling Pathways in the Cotyledonary Artery of Cow Placentomes

Placenta

Volumn 28, Issue 4, 2007, Pages 361-368

  Zhu, M J ^a   Du, M ^a   Hess, B W ^a   Means, W J ^a   Nathanielsz, P W ^a,b   Ford, S P ^a  

^a UNIVERSITY OF WYOMING   (United States)

^b UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

Author keywords

Akt and ERK1 2 phosphorylation; Cow; Nutrient restriction; Placentome vascularity

Indexed keywords

MITOGEN ACTIVATED PROTEIN KINASE 1; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN KINASE B;

ANGIOGENESIS; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; COW; ENZYME PHOSPHORYLATION; FEMALE; GESTATION PERIOD; NONHUMAN; NUTRIENT; PLACENTA CIRCULATION; PLACENTA WEIGHT; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; UPREGULATION;

1-PHOSPHATIDYLINOSITOL 3-KINASE; ANIMAL NUTRITION PHYSIOLOGY; ANIMALS; CATTLE; EXTRACELLULAR SIGNAL-REGULATED MAP KINASES; FEMALE; FETAL WEIGHT; FOOD DEPRIVATION; GESTATIONAL AGE; NEOVASCULARIZATION, PHYSIOLOGIC; ORGAN SIZE; PHOSPHORYLATION; PLACENTA; PLACENTAL CIRCULATION; PREGNANCY; SIGNAL TRANSDUCTION;

EID: 33947729127     PISSN: 01434004     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.placenta.2006.04.005     Document Type: Article

References (41)

1. Ford S.P. Cotyledonary placenta. In: Knobil E., and Neil J.D. (Eds). Encyclopedia of Reproduction vol. 1 (2000), Academic Press, San Diego, CA 730-738
2. Ford S.P., Vonnahme K.A., Drumhiller M.C., Reynolds L.P., Nijland M.J., and Nathanielsz P.W. Arteriolar and capillary volume increase as placentomes advance from type A through type D developmental stages. Proc Soc Study Reprod (2004) Vancouver, B.C. Canada
3. Reynolds L.P., and Redmer D.A. Utero-placental vascular development and placental function. J Anim Sci 73 (1995) 1839-1851
4. Bjorkman N.H. Light and electron microscopic studies on cellular alterations in the normal bovine placentome. Anat Rec 163 (1969) 17-29
5. Leiser R., Krebs C., Klisch K., Ebert B., Dantzer V., Schuler G., et al. Fetal villosity and microvasculature of the bovine placentome in the second half of gestation. J Anat 191 Pt 4 (1997) 517-527
6. Ramsey E.M. The Placenta, Human and Animal (1982), Praeger, New York
7. Ford S.P. Control of blood flow to the gravid uterus of domestic livestock species. J Anim Sci 73 (1995) 1852-1860
8. Reynolds L.P., and Redmer D.A. Angiogenesis in the placenta. Biol Reprod 64 (2001) 1033-1040
9. Vonnahme K.A., Hess B.W., Hansen T.R., McCormick R.J., Rule D.C., Moss G.E., et al. Maternal undernutrition from early- to mid-gestation leads to growth retardation, cardiac ventricular hypertrophy, and increased liver weight in the fetal sheep. Biol Reprod 69 (2003) 133-140
10. Wallace J.M., Regnault T.R., Limesand S.W., Hay Jr. W.W., and Anthony R.V. Investigating the causes of low birth weight in contrasting ovine paradigms. J Physiol 565 (2005) 19-26
11. Regnault T.R., Friedman J.E., Wilkening R.B., Anthony R.V., and Hay Jr. W.W. Fetoplacental transport and utilization of amino acids in IUGR-a review. Placenta 26 Suppl A (2005) S52-S62
12. Gilbert J.S., Lang A.L., and Nijland M.J. Maternal nutrient restriction and the fetal left ventricle: decreased angiotensin receptor expression. Reprod Biol Endocrinol 3 (2005) 27
13. Castilla M.A., Neria F., Renedo G., Pereira D.S., Gonzalez-Pacheco F.R., Jimenez S., et al. Tumor-induced endothelial cell activation: role of vascular endothelial growth factor. Am J Physiol Cell Physiol 286 (2004) C1170-C1176
14. Radcliff K., Tang T.B., Lim J., Zhang Z., Abedin M., Demer L.L., et al. Insulin-like growth factor-I regulates proliferation and osteoblastic differentiation of calcifying vascular cells via extracellular signal-regulated protein kinase and phosphatidylinositol 3-kinase pathways. Circ Res 96 (2005) 398-400
15. Sturgill T.W., Ray L.B., Erikson E., and Maller J.L. Insulin-stimulated MAP-2 kinase phosphorylates and activates ribosomal protein S6 kinase II. Nature 334 (1988) 715-718
16. Payne D.M., Rossomando A.J., Martino P., Erickson A.K., Her J.H., Shabanowitz J., et al. Identification of the regulatory phosphorylation sites in pp42/mitogen-activated protein kinase (MAP kinase). Embo J 10 (1991) 885-892
17. Alessi D.R., Andjelkovic M., Caudwell B., Cron P., Morrice N., Cohen P., et al. Mechanism of activation of protein kinase B by insulin and IGF-1. Embo J 15 (1996) 6541-6551
18. Meadows K.N., Bryant P., Vincent P.A., and Pumiglia K.M. Activated Ras induces a proangiogenic phenotype in primary endothelial cells. Oncogene 23 (2004) 192-200
19. Li W., and Sumpio B.E. Strain-induced vascular endothelial cell proliferation requires PI3K-dependent mTOR-4E-BP1 signal pathway. Am J Physiol Heart Circ Physiol 288 (2005) H1591-H1597
20. Yang X., Zhu M.J., Sreejayan N., Ren J., and Du M. Angiotensin II promotes smooth muscle cells proliferation and migration through release of heparin-binding epidermal growth factor and activation of EGF-receptor pathway. Mol Cells 20 (2005) 263-270
21. NRC. Nutrient Requirements of Beef Cattle, vol. 7th ed. (1996), National Academic Press, Washington, DC
22. Du M., Zhu M.J., Means W.J., Hess B.W., and Ford S.P. Effect of nutrient restriction on calpain and calpastatin content of skeletal muscle from cows and fetuses. J Anim Sci 82 (2004) 2541-2547
23. Zhu M.J., Ford S.P., Nathanielsz P.W., and Du M. Effect of maternal nutrient restriction in sheep on the development of fetal skeletal muscle. Biol Reprod 71 (2004) 1968-1973
24. Institute S. SAS User's Guide. Version 8 (2000), SAS Institute Inc., Cary, NC
25. Reynolds L.P., Borowicz P.P., Vonnahme K.A., Johnson M.L., Grazul-Bilska A.T., Redmer D.A., et al. Placental angiogenesis in sheep models of compromised pregnancy. J Physiol 565 (2005) 43-58
26. Gerber H.P., McMurtrey A., Kowalski J., Yan M., Keyt B.A., Dixit V., et al. Vascular endothelial growth factor regulates endothelial cell survival through the phosphatidylinositol 3′-kinase/Akt signal transduction pathway. Requirement for Flk-1/KDR activation. J Biol Chem 273 (1998) 30336-30343
27. Fujio Y., and Walsh K. Akt mediates cytoprotection of endothelial cells by vascular endothelial growth factor in an anchorage-dependent manner. J Biol Chem 274 (1999) 16349-16354
28. Shiojima I., and Walsh K. Role of Akt signaling in vascular homeostasis and angiogenesis. Circ Res 90 (2002) 1243-1250
29. Yang Z.Z., Tschopp O., Hemmings-Mieszczak M., Feng J., Brodbeck D., Perentes E., et al. Protein kinase B alpha/Akt1 regulates placental development and fetal growth. J Biol Chem 278 (2003) 32124-32131
30. Ma L., Chen Z., Erdjument-Bromage H., Tempst P., and Pandolfi P.P. Phosphorylation and functional inactivation of TSC2 by Erk implications for tuberous sclerosis and cancer pathogenesis. Cell 121 (2005) 179-193
31. Zheng J., Wen Y., Austin J.L., and Chen D.B. Exogenous nitric oxide stimulates cell proliferation via activation of a mitogen-activated protein kinase pathway in ovine fetoplacental artery endothelial cells. Biol Reprod (2005)
32. Morris N.H., Eaton B.M., and Dekker G. Nitric oxide, the endothelium, pregnancy and pre-eclampsia. Br J Obstet Gynaecol 103 (1996) 4-15
33. Sladek S.M., Magness R.R., and Conrad K.P. Nitric oxide and pregnancy. Am J Physiol 272 (1997) R441-R463
34. Ziche M., Morbidelli L., Choudhuri R., Zhang H.T., Donnini S., Granger H.J., et al. Nitric oxide synthase lies downstream from vascular endothelial growth factor-induced but not basic fibroblast growth factor-induced angiogenesis. J Clin Invest 99 (1997) 2625-2634
35. Parenti A., Morbidelli L., Cui X.L., Douglas J.G., Hood J.D., Granger H.J., et al. Nitric oxide is an upstream signal of vascular endothelial growth factor-induced extracellular signal-regulated kinase1/2 activation in postcapillary endothelium. J Biol Chem 273 (1998) 4220-4226
36. Kawasaki K., Smith Jr. R.S., Hsieh C.M., Sun J., Chao J., and Liao J.K. Activation of the phosphatidylinositol 3-kinase/protein kinase Akt pathway mediates nitric oxide-induced endothelial cell migration and angiogenesis. Mol Cell Biol 23 (2003) 5726-5737
37. Babaei S., Teichert-Kuliszewska K., Monge J.C., Mohamed F., Bendeck M.P., and Stewart D.J. Role of nitric oxide in the angiogenic response in vitro to basic fibroblast growth factor. Circ Res 82 (1998) 1007-1015
38. Laviola L., Perrini S., Belsanti G., Natalicchio A., Montrone C., Leonardini A., et al. Intrauterine growth restriction in humans is associated with abnormalities in placental insulin-like growth factor signaling. Endocrinology 146 (2005) 1498-1505
39. Avruch J., Lin Y., Long X., Murthy S., and Ortiz-Vega S. Recent advances in the regulation of the TOR pathway by insulin and nutrients. Curr Opin Clin Nutr Metab Care 8 (2005) 67-72
40. Boileau P., Cauzac M., Pereira M.A., Girard J., and Hauguel-De Mouzon S. Dissociation between insulin-mediated signaling pathways and biological effects in placental cells: role of protein kinase B and MAPK phosphorylation. Endocrinology 142 (2001) 3974-3979
41. Desai J., Holt-Shore V., Torry R.J., Caudle M.R., and Torry D.S. Signal transduction and biological function of placenta growth factor in primary human trophoblast. Biol Reprod 60 (1999) 887-892