Deletion of Kelch-like ECH-associated Protein 1 (Keap1) in Kidney Epithelial Cells Causes Hydronephrosis in Mice

Case ID:
C13124

Invention novelty:

This invention reveals an unexpected, novel kelch-like ECH-associated protein 1 (KEAP 1) mediated signaling pathway in renal development.

 

Value Proposition:

The Nrf2-Keap1 pathway has an important role in both acute kidney injury (AKI) and chronic kidney disease (CKD). This pathway has a key regulatory function on many antioxidant and stress pathways, including heme oxygenase. This technology identifies KEAP 1 as factor involved in cyst formation and hydronephrosis during kidney development, which is advantageous for:

•       Studying kidney development

•       The role of the KEAP 1 pathway in kidney repair and regeneration.

 

Technical Details:

Johns Hopkins researchers have discovered a novel role for KEAP1 mediated signaling pathway in renal development. They have identified that absence of KEAP1 in renal tubular epithelial cells significantly affects normal kidney development in a fashion consistent with hydronephrosis. Kidney epithelial cell specific Keap1-deficient (Ksp-Keap1-KO) mice were generated by crossing Ksp-Cre with Keap1 floxed (Keap1fl/fl) mice. A comprehensive histological examination along with detailed hematological, biochemical and urinary analysis was performed to evaluate these mice

 

Looking for Partners:

To develop & commercialize the technology as a research/discovery tool to aid in the development of therapeutics for acute kidney injury and chronic kidney disease.

 

Stage of Development: Tangible material

 

Data Availability: Animal Data

 

Publication(s)/Associated Cases: JHU: C13210,  J Am Soc Nephrol. 2015 Dec;26(12):2989-3000

 

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For Information, Contact:
Nakisha Holder
nickki@jhu.edu
410-614-0300
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