TY - JOUR
T1 - Nuclear hormone receptors in podocytes
AU - Khurana, Simran
AU - Bruggeman, Leslie A.
AU - Kao, Hung Ying
N1 - Funding Information:
We thank Dr. David Samols for his comments on the manuscript. H.-Y. Kao is supported by NIH, R01 DK078965 and HL093269.
PY - 2012/9/20
Y1 - 2012/9/20
N2 - Nuclear receptors are a family of ligand-activated, DNA sequence-specific transcription factors that regulate various aspects of animal development, cell proliferation, differentiation, and homeostasis. The physiological roles of nuclear receptors and their ligands have been intensively studied in cancer and metabolic syndrome. However, their role in kidney diseases is still evolving, despite their ligands being used clinically to treat renal diseases for decades. This review will discuss the progress of our understanding of the role of nuclear receptors and their ligands in kidney physiology with emphasis on their roles in treating glomerular disorders and podocyte injury repair responses.
AB - Nuclear receptors are a family of ligand-activated, DNA sequence-specific transcription factors that regulate various aspects of animal development, cell proliferation, differentiation, and homeostasis. The physiological roles of nuclear receptors and their ligands have been intensively studied in cancer and metabolic syndrome. However, their role in kidney diseases is still evolving, despite their ligands being used clinically to treat renal diseases for decades. This review will discuss the progress of our understanding of the role of nuclear receptors and their ligands in kidney physiology with emphasis on their roles in treating glomerular disorders and podocyte injury repair responses.
UR - http://www.scopus.com/inward/record.url?scp=84872315073&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84872315073&partnerID=8YFLogxK
U2 - 10.1186/2045-3701-2-33
DO - 10.1186/2045-3701-2-33
M3 - Review article
C2 - 22995171
AN - SCOPUS:84872315073
SN - 2045-3701
VL - 2
JO - Cell and Bioscience
JF - Cell and Bioscience
IS - 1
M1 - 33
ER -