Grant: CIHR Fellowship
Direct Payment
$150,000.00
Investigating Osteoclast Dysfunction as an Underlying Cause of Low Bone Mass in Lysinuric Protein Intolerance (LPI)
FY 2023-24
Summary
Lysinuric protein intolerance (LPI) is a life-threatening inherited disease that can affect multiple organs and tissues in the body. LPI is caused by genetic variations in a gene called SLC7A7, which plays an important role in transporting specific amino acids from our diet in the body. Altered SLC7A7 function leads to a range of problems, like poor growth, elevated ammonia in the blood, immune system disorders, and reduced bone mass in children and young adults. The goal of my research is to investigate the cause of low bone mass in LPI. Specifically, I will test whether the function of osteoclasts, a type of cell that breaks down bone, is altered in a mouse model for LPI. If we confirm altered function of osteoclasts in these mice, my research findings will support the development of therapies targeting the osteoclasts for low bone mass in LPI. Additionally, the findings from my work will also shed light on the roles of amino acid transport and nutrition in osteoclasts and other bone cells, and these findings could have impacts on more common bone disorders.
Department
Program
CIHR Fellowship
Recipient
Location
Texas, United States of America
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
492696
Name
Zhouyao Haonan
Region
Texas
Country
United States of America
Orgtype
Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
Investigating Osteoclast Dysfunction as an Underlying Cause of Low Bone Mass in Lysinuric Protein Intolerance (LPI)
Programtype2
Fellowship Programs
Orgnameinp2
Direct Payment
Cihramount2
$150,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Amino Acid Transport; Bone Histology; Inborn Errors Of Metabolism; Low Bone Mass; Lysinuric Protein Intolerance; Osteoblasts; Osteoclasts; Osteoporosis; Slc7a7; Urea Cycle Dysfunction
Abstract
Lysinuric protein intolerance (LPI) is a life-threatening inherited disease that can affect multiple organs and tissues in the body. LPI is caused by genetic variations in a gene called SLC7A7, which plays an important role in transporting specific amino acids from our diet in the body. Altered SLC7A7 function leads to a range of problems, like poor growth, elevated ammonia in the blood, immune system disorders, and reduced bone mass in children and young adults. The goal of my research is to investigate the cause of low bone mass in LPI. Specifically, I will test whether the function of osteoclasts, a type of cell that breaks down bone, is altered in a mouse model for LPI. If we confirm altered function of osteoclasts in these mice, my research findings will support the development of therapies targeting the osteoclasts for low bone mass in LPI. Additionally, the findings from my work will also shed light on the roles of amino acid transport and nutrition in osteoclasts and other bone cells, and these findings could have impacts on more common bone disorders.
Competitiondate
202310
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Zhouyao, Haonan
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $150,000~ $0~