During early embryonic development (E12-14) renin expressing cells are present in the undifferentiated metanephric mesenchyme before kidney vascularization has occurred and before the hemodynamic functions of renin are needed. Later in fetal life (E17-20) renin expressing cells are found in large intrarenal arteries. As maturating continues, renin-expressing cells become progressively restricted to the classical juxtaglomerular localization found in the adult mammal. If an adult mammal is subjected to manipulations known to increase renin synthesis, there is a recruitment of renin expressing cells along the preglomerular arteries and in the kidney interstitium resembling the embryonic pattern. These data suggest that renal vascular and interstitium cells have the plasticity to develop phenotypic characterizations of renin expressing cells. It is likely that the ability of adult kidney cells to re-express the renin gene and acquire the JG cell phenotype depends on the developmental history of the cell in question. However, the embryologic origin and the functions of JG cells during kidney embryogenesis are unknown. We hypothesis that (1) the JG cells originate from the kidney cells rather than from invading extrarenal vessels, (2) The lineage of JG cells is that of smooth muscle or interstitial cells, (3) Expression of renin is responsible of JG cell differentiation, (4) JG cells are involved in nephrogenesis and microvascular development of the kidney. The following specific aims will be pursued: (i) Define the phenotypic characteristics of JG cells during maturation, (ii) Determine the site of origin of JG cells; (iii) Identify and follow the fate of JG cell precursors in vitro and in vivo; (iv) Define whether the JG cell is necessary for normal nephrogenesis and vascular development. The studies should generate fundamental knowledge on JG cell differentiation and function during kidney embryogenesis. By providing new models, the studies should also open new avenues for understanding, treatment and prevention of hypertension and kidney diseases.

Project Start
1999-09-01
Project End
2000-08-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
3
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Virginia
Department
Type
DUNS #
001910777
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Gomez, R Ariel; Belyea, Brian; Medrano, Silvia et al. (2014) Fate and plasticity of renin precursors in development and disease. Pediatr Nephrol 29:721-6
Jose, Pedro A; Soares-da-Silva, Patricio; Eisner, Gilbert M et al. (2010) Dopamine and G protein-coupled receptor kinase 4 in the kidney: role in blood pressure regulation. Biochim Biophys Acta 1802:1259-67
Lysiak, Jeffrey J; Kirby, Jennifer L; Tremblay, Jacques J et al. (2009) Hypoxia-inducible factor-1alpha is constitutively expressed in murine Leydig cells and regulates 3beta-hydroxysteroid dehydrogenase type 1 promoter activity. J Androl 30:146-56
Reinking, Benjamin E; Wedemeyer, Elesa W; Weiss, Robert M et al. (2009) Cardiomyopathy in offspring of diabetic rats is associated with activation of the MAPK and apoptotic pathways. Cardiovasc Diabetol 8:43
Hinze, Claas H; Suzuki, Michiko; Klein-Gitelman, Marisa et al. (2009) Neutrophil gelatinase-associated lipocalin is a predictor of the course of global and renal childhood-onset systemic lupus erythematosus disease activity. Arthritis Rheum 60:2772-81
Zeng, Chunyu; Asico, Laureano D; Yu, Changqing et al. (2008) Renal D3 dopamine receptor stimulation induces natriuresis by endothelin B receptor interactions. Kidney Int 74:750-9
Li, Hewang; Li, Hui-Fang; Felder, Robin A et al. (2008) Rab4 and Rab11 coordinately regulate the recycling of angiotensin II type I receptor as demonstrated by fluorescence resonance energy transfer microscopy. J Biomed Opt 13:031206
Zeng, Chunyu; Armando, Ines; Luo, Yingjin et al. (2008) Dysregulation of dopamine-dependent mechanisms as a determinant of hypertension: studies in dopamine receptor knockout mice. Am J Physiol Heart Circ Physiol 294:H551-69
Pentz, Ellen Steward; Lopez, Maria Luisa S Sequeira; Cordaillat, Magali et al. (2008) Identity of the renin cell is mediated by cAMP and chromatin remodeling: an in vitro model for studying cell recruitment and plasticity. Am J Physiol Heart Circ Physiol 294:H699-707
Gildea, John J; Wang, Xiaoli; Jose, Pedro A et al. (2008) Differential D1 and D5 receptor regulation and degradation of the angiotensin type 1 receptor. Hypertension 51:360-6

Showing the most recent 10 out of 130 publications