Renal function is dependent on the correct association and alignment of at least 14 unique transporting epithelial cell types into glomerular and tubular segments. These hetrrogeneous cell types are derived from the undifferentiated mesenchymal cells present in the embryonic metanephric kidney anlage. Mesenchymal cells could be stem cells that generate all renal cell types or mesenchymal ells might be a heterogeneous group of cells each differentiating directly into unique renal cell types. To distinguish between these models, the lac-Z gene was introduced into individual mephrogenic mesenchymal cells (rat, gestation cay 13) using replication defective retroviruses and their progeny were identified after differentiation in vitro. The clonal progeny of individual tagged cells were found to reside in glomerulus and proximal tubule segments of single nephron. These results demonstrate that the metanephric mesenchyme contains multipotent nephrogenic stem cells. A library of stem ell specific monoclonal antibodies will be prepared to characterize this newly ientified stem cell, and used to follow its fate during differentiation. Cell culture conditions will be defined that support the proliferation of these stem cells. In addition these cells will be immortalized and clonal cell lines established. These reagents and cell lines will be used to identify and characterize the regulatory mechanisms mediating the conversion of an undifferentiated mesenchymal cell into diverse renal epithelial celll types.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK045218-03
Application #
3246735
Study Section
General Medicine B Study Section (GMB)
Project Start
1991-09-15
Project End
1994-08-31
Budget Start
1993-09-01
Budget End
1994-08-31
Support Year
3
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Type
Schools of Medicine
DUNS #
201373169
City
New York
State
NY
Country
United States
Zip Code
10065
Lacko, Lauretta A; Hurtado, Romulo; Hinds, Samantha et al. (2017) Altered feto-placental vascularization, feto-placental malperfusion and fetal growth restriction in mice with Egfl7 loss of function. Development 144:2469-2479
Hurtado, Romulo; Smith, Carl S (2016) Hyperpolarization-activated cation and T-type calcium ion channel expression in porcine and human renal pacemaker tissues. J Anat 228:812-25
Hurtado, Romulo; Zewdu, Rediet; Mtui, James et al. (2015) Pbx1-dependent control of VMC differentiation kinetics underlies gross renal vascular patterning. Development 142:2653-64
Herzlinger, Doris; Hurtado, Romulo (2014) Patterning the renal vascular bed. Semin Cell Dev Biol 36:50-6
Hurtado, Romulo; Bub, Gil; Herzlinger, Doris (2014) A molecular signature of tissues with pacemaker activity in the heart and upper urinary tract involves coexpressed hyperpolarization-activated cation and T-type Ca2+ channels. FASEB J 28:730-9
Grinstein, Mor; Yelin, Ronit; Herzlinger, Doris et al. (2013) Generation of the podocyte and tubular components of an amniote kidney: timing of specification and a role for Wnt signaling. Development 140:4565-73
Herzlinger, Doris (2011) Upper urinary tract pacemaker cells join the GLI club. J Clin Invest 121:836-8
Hurtado, Romulo; Bub, Gil; Herzlinger, Doris (2010) The pelvis-kidney junction contains HCN3, a hyperpolarization-activated cation channel that triggers ureter peristalsis. Kidney Int 77:500-8
Wang, Gerald J; Brenner-Anantharam, Andrea; Vaughan, E Darracott et al. (2009) Antagonism of BMP4 signaling disrupts smooth muscle investment of the ureter and ureteropelvic junction. J Urol 181:401-7
Guillaume, Richard; Bressan, Michel; Herzlinger, Doris (2009) Paraxial mesoderm contributes stromal cells to the developing kidney. Dev Biol 329:169-75

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