Acute kidney injury and chronic kidney disease are major US and global health problems and represent a sig- nificant contributor to all cause morbidity and mortality. These two disease states are interconnected and inter- dependent, the downstream effect of which is the alarming rise in chronic kidney disease worldwide. At the heart of these disease states is the response to injury and dysregulated wound repair leading to fibrosis and loss of organ function. Currently, there are no therapies for these two diseases due to our incomplete knowledge of how to uncouple the maladaptive responses. Scarless wound repair with regeneration is the ho- ly grail of wound healing, and thought to be restricted to amphibians and lower vertebrates. However, all mammalian species exhibit scar-free wound repair as embryos that is lost after birth and instead exhibit scar formation, tissue fibrosis, and loss of organ function. However, the ?Old World? clade of muroid rodents of the genus Acomys (common name-African Spiny Mouse) evolved a different course of wound repair in their native habitat of northern Africa and the Middle East. Acomys can shed up to 60% of its skin to avoid predators and then amazingly regenerate their skin without fibrosis or scarring. Acomys represent the highest vertebrate class known to exhibit tissue regeneration without scar formation as adults. In this proposal, our objective is to determine if this remarkable course of wound repair extends into the kidney. Our preliminary data suggests that evolutionary-derived genomic adaptations in Acomys lead to scarless regenerative wound repair in re- sponse to acute and chronic kidney injury. We will validate this observation using complementary strategies in vitro and in vivo and begin to define the pathways that unlock the regenerative potential of Acomys during kid- ney injury. The results of our proposed studies have the potential to transform current research and reveal tru- ly novel insights with exciting possibilities for discovery not only in kidney fibrosis but other organs as well.

Public Health Relevance

Acute and chronic kidney injury leads to fibrosis and loss of organ function with no therapeutic options to stop or reverse its progression. A careful dissection of the scarless, regenerative wound repair paradigm in Acomys in response to kidney injury will uncover elegant evolutionary adaptations and lead to novel therapeutics.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK114149-02
Application #
9783803
Study Section
Pathobiology of Kidney Disease Study Section (PBKD)
Program Officer
Hoshizaki, Deborah K
Project Start
2018-09-15
Project End
2021-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Seattle Children's Hospital
Department
Type
DUNS #
048682157
City
Seattle
State
WA
Country
United States
Zip Code
98105