Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-26T07:56:24.346Z Has data issue: false hasContentIssue false

Long-term effects of maternal undernutrition on offspring carotid artery remodeling: role of miR-29c

Published online by Cambridge University Press:  26 May 2015

O. Khorram*
Affiliation:
Department of Obstetrics and Gynecology, Harbor-UCLA Medical Center, Torrance, CA, USA
T. D. Chuang
Affiliation:
Department of Obstetrics and Gynecology, Harbor-UCLA Medical Center, Torrance, CA, USA
W. J. Pearce
Affiliation:
Department of Physiology and Center for Perinatal Biology, Loma Linda University, CA, USA
*
*Address for correspondence: O. Khorram, MD, PhD, Department of Obstetrics and Gynecology, Harbor-UCLA Medical Center, 1000 W. Carson St, Box 489, Torrance, CA 90502, USA. (Email okhorram@obgyn.humc.edu)

Abstract

The purpose of this study was to examine the hypothesis that excess maternal glucocorticoids in response to maternal undernutrition programs the expression of extracellular matrix (ECM) components potentially by miR-29c. We measured the expression of mRNA (qRT-PCR) and protein (Western blot) for collagen 3A1, collagen 4A5 and matrix metalloproteinase 2 (MMP2) in offspring carotid arteries from three groups of dams: 50% food-restricted in latter half of gestation [maternal undernutrition (MUN)], MUN dams who received metyrapone (MET) (500 mg/ml ) in drinking water from day 10 of gestation to term, and control dams fed an ad libitum diet. The expression of miR-29c was significantly decreased at 3 weeks, 3 months and 9 months in MUN carotid arteries, and these decreases in expression were partially blocked by treatment of dams with MET. The expression pattern of ECM genes that are targets of miR-29c correlated with miR-29c expression. Expression of mRNA was increased for elastin (ELN) and MMP2 mRNA in 3-week MUN carotids; in 9-month carotids there were also significant increases in expression of Col3A1 and Col4A5. These changes in mRNA expression of ECM genes at 3 weeks and 9 months were blocked by MET treatment. Similarly, the expression of ELN and MMP2 proteins at 3 weeks were increased in MUN carotids, and by 9 months there were also increases in expression of Col3A1 and Col4A5, which were blocked by MET in MUN carotids. Overall, the results demonstrate a close correlation between expression of miR-29c and the ECM proteins that are its targets thus supporting our central hypothesis.

Type
Original Article
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2015 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Barker, DJ, Osmond, C, Golding, J, Kuh, D, Wadsworth, ME. Growth in utero, blood pressure in childhood and adult life, and mortality from cardiovascular disease. Br Med J. 1989; 298, 564567.Google Scholar
2. McMillen, IC, Robinson, JS. Developmental origins of the metabolic syndrome: prediction, plasticity, and programming. Physiol Rev. 2005; 85, 571633.Google Scholar
3. Langley-Evans, SC, McMullen, S. Developmental origins of adult disease. Med Princ Pract. 2010; 19, 8798.Google Scholar
4. Harris, A, Seckl, J. Glucocorticoids, prenatal stress and the programming of disease. Horm Behav. 2011; 59, 279289.Google Scholar
5. Seckl, JR. Prenatal glucocorticoids and long-term programming. Eur J Endocrinol. 2004; 151(Suppl. 3), U49U62.Google Scholar
6. Gardner, DS, Jackson, AA, Langley-Evans, SC. Maintenance of maternal diet-induced hypertension in the rat is dependent on glucocorticoids. Hypertension. 1997; 30, 15251530.Google Scholar
7. Langley-Evans, SC. Hypertension induced by foetal exposure to a maternal low-protein diet, in the rat, is prevented by pharmacological blockade of maternal glucocorticoid synthesis. J Hypertens. 1997; 15, 537544.Google Scholar
8. Khorram, O, Momeni, M, Desai, M, Ross, MG. Nutrient restriction in utero induces remodeling of the vascular extracellular matrix in rat offspring. Reprod Sci. 2007; 14, 7380.Google Scholar
9. Khorram, O, Momeni, M, Ferrini, M, Desai, M, Ross, MG. In utero undernutrition in rats induces increased vascular smooth muscle content in the offspring. Am J Obstet Gynecol. 2007; 196, 486488.Google Scholar
10. Durrant, LM, Khorram, O, Buchholz, JN, Pearce, WJ. Maternal food restriction modulates cerebrovascular structure and contractility in adult rat offspring: effects of metyrapone. Am J Physiol Regul Integr Comp Physiol. 2014; 306, R401R410.Google Scholar
11. Hemmings, DG, Williams, SJ, Davidge, ST. Increased myogenic tone in 7-month-old adult male but not female offspring from rat dams exposed to hypoxia during pregnancy. Am J Physiol Heart Circ Physiol. 2005; 289, H674H682.Google Scholar
12. Torrens, C, Brawley, L, Barker, AC, et al. Maternal protein restriction in the rat impairs resistance artery but not conduit artery function in pregnant offspring. J Physiol. 2003; 547, 7784.Google Scholar
13. Williams, SJ, Campbell, ME, McMillen, IC, Davidge, ST. Differential effects of maternal hypoxia or nutrient restriction on carotid and femoral vascular function in neonatal rats. Am J Physiol Regul Integr Comp Physiol. 2005; 288, R360R367.Google Scholar
14. Khorram, O, Khorram, N, Momeni, M, et al. Maternal undernutrition inhibits angiogenesis in the offspring: a potential mechanism of programmed hypertension. Am J Physiol Regul Integr Comp Physiol. 2007; 293, R745R753.Google Scholar
15. Ambros, V. The functions of animal microRNAs. Nature. 2004; 431, 350355.Google Scholar
16. Khorram, O, Han, G, Bagherpour, R, et al. Effect of maternal undernutrition on vascular expression of micro and messenger RNA in newborn and aging offspring. Am J Physiol Regul Integr Comp Physiol. 2010; 298, R1366R1374.Google Scholar
17. Desai, M, Gayle, D, Babu, J, Ross, MG. Programmed obesity in intrauterine growth-restricted newborns: modulation by newborn nutrition. Am J Physiol Regul Integr Comp Physiol. 2005; 288, R91R96.CrossRefGoogle ScholarPubMed
18. Warnes, KE, McMillen, IC, Robinson, JS, Coulter, CL. Metyrapone infusion stimulates adrenal growth without activating the cell cycle or the IGF system in the late gestation fetal sheep. Endocr Res. 2004; 30, 535539.Google Scholar
19. Khorram, O, Ghazi, R, Chuang, TD, et al. Excess maternal glucocorticoids in response to in utero undernutrition inhibit offspring angiogenesis. Reprod Sci. 2014; 21, 601611.Google Scholar
20. Liu, Y, Taylor, NE, Lu, L, et al. Renal medullary microRNAs in Dahl salt-sensitive rats: miR-29b regulates several collagens and related genes. Hypertension. 2010; 55, 974982.Google Scholar
21. Wang, H, Zhu, Y, Zhao, M, et al. miRNA-29c suppresses lung cancer cell adhesion to extracellular matrix and metastasis by targeting integrin beta1 and matrix metalloproteinase2 (MMP2). PLoS One. 2013; 8, e70192.Google Scholar
22. Shadwick, RE. Mechanical design in arteries. J Exp Biol. 1999; 202, 33053313.Google Scholar
23. Wagenseil, JE, Mecham, RP. Vascular extracellular matrix and arterial mechanics. Physiol Rev. 2009; 89, 957989.Google Scholar
24. Karnik, SK, Brooke, BS, Bayes-Genis, A, et al. A critical role for elastin signaling in vascular morphogenesis and disease. Development. 2003; 130, 411423.CrossRefGoogle ScholarPubMed
25. Anceschi, MM, Palmerini, CA, Codini, M, Luzi, P, Cosmi, EV. Collagen and elastin in rabbit fetal lung: ontogeny and effects of steroids. J Dev Physiol. 1992; 18, 233236.Google Scholar
26. Nakamura, T, Liu, M, Mourgeon, E, Slutsky, A, Post, M. Mechanical strain and dexamethasone selectively increase surfactant protein C and tropoelastin gene expression. Am J Physiol Lung Cell Mol Physiol. 2000; 278, L974L980.Google Scholar
27. Keeley, FW, Johnson, DJ. Age differences in the effect of hydrocortisone on the synthesis of insoluble elastin in aortic tissue of growing chicks. Connect Tissue Res. 1987; 16, 259268.Google Scholar
28. Del, MM, Covello, SP, Kennedy, SH, et al. Identification of novel glucocorticoid-response elements in human elastin promoter and demonstration of nucleotide sequence specificity of the receptor binding. J Invest Dermatol. 1997; 108, 938942.Google Scholar
29. van, RE, Sutherland, LB, Thatcher, JE, et al. Dysregulation of microRNAs after myocardial infarction reveals a role of miR-29 in cardiac fibrosis. Proc Natl Acad Sci USA. 2008; 105, 1302713032.Google Scholar
30. Shoulders, MD, Raines, RT. Collagen structure and stability. Annu Rev Biochem. 2009; 78, 929958.Google Scholar
31. Brawley, L, Itoh, S, Torrens, C, et al. Dietary protein restriction in pregnancy induces hypertension and vascular defects in rat male offspring. Pediatr Res. 2003; 54, 8390.Google Scholar
32. Sathishkumar, K, Elkins, R, Yallampalli, U, Yallampalli, C. Protein restriction during pregnancy induces hypertension and impairs endothelium-dependent vascular function in adult female offspring. J Vasc Res. 2009; 46, 229239.Google Scholar
33. Leitman, DC, Benson, SC, Johnson, LK. Glucocorticoids stimulate collagen and noncollagen protein synthesis in cultured vascular smooth muscle cells. J Cell Biol. 1984; 98, 541549.Google Scholar
34. Poiani, GJ, Tozzi, CA, Thakker-Varia, S, Choe, JK, Riley, DJ. Effect of glucocorticoids on collagen accumulation in pulmonary vascular remodeling in the rat. Am J Respir Crit Care Med. 1994; 149, 994999.Google Scholar
35. Jacob, MP. Extracellular matrix remodeling and matrix metalloproteinases in the vascular wall during aging and in pathological conditions. Biomed Pharmacother. 2003; 57, 195202.Google Scholar
36. Yasmin, Mc, Eniery, CM, Wallace, S, et al. Matrix metalloproteinase-9 (MMP-9), MMP-2, and serum elastase activity are associated with systolic hypertension and arterial stiffness. Arterioscler Thromb Vasc Biol. 2005; 25, 372.Google Scholar
37. Intengan, HD, Schiffrin, EL. Vascular remodeling in hypertension: roles of apoptosis, inflammation, and fibrosis. Hypertension. 2001; 38, 581587.Google Scholar
38. Roomi, MW, Kalinovsky, T, Monterrey, J, Rath, M, Niedzwiecki, A. In vitro modulation of MMP-2 and MMP-9 in adult human sarcoma cell lines by cytokines, inducers and inhibitors. Int J Oncol. 2013; 43, 17871798.Google Scholar
39. Yigit, O, Acioglu, E, Gelisgen, R, et al. The effect of corticosteroid on metalloproteinase levels of nasal polyposis. Laryngoscope. 2011; 121, 667673.Google Scholar
40. Touyz, RM. Intracellular mechanisms involved in vascular remodelling of resistance arteries in hypertension: role of angiotensin II. Exp Physiol. 2005; 90, 449455.Google Scholar
41. De Mey, JG, Schiffers, PM, Hilgers, RH, Sanders, MM. Toward functional genomics of flow-induced outward remodeling of resistance arteries. Am J Physiol Heart Circ Physiol. 2005; 288, H1022H1027.Google Scholar
42. Pelisek, J, Eckstein, HH, Zernecke, A. Pathophysiological mechanisms of carotid plaque vulnerability: impact on ischemic stroke. Arch Immunol Ther Exp (Warsz ). 2012; 60, 431442.Google Scholar
43. Goncalves, I, Moses, J, Dias, N, et al. Changes related to age and cerebrovascular symptoms in the extracellular matrix of human carotid plaques. Stroke. 2003; 34, 616622.Google Scholar
44. Paek, DS, Sakurai, R, Saraswat, A, et al. Metyrapone alleviates deleterious effects of maternal food restriction on lung development and growth of rat offspring. Reprod Sci. 2015; 22, 207222.Google Scholar
45. Rehan, VK, Li, Y, Corral, J, et al. Metyrapone blocks maternal food restriction-induced changes in female rat offspring lung development. Reprod Sci. 2014; 21, 517525.Google Scholar