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Active NON-SBIR/STTR RPGS NIH (US)

Investigating spatial and temporal heterogeneity in mitochondria during aging using in vivo high-content chemical imaging

$1.97M USD

Funder NATIONAL INSTITUTE ON AGING
Recipient Organization Georgia Institute of Technology
Country United States
Start Date Aug 01, 2024
End Date Apr 30, 2026
Duration 637 days
Number of Grantees 3
Roles Principal Investigator; Co-Investigator
Data Source NIH (US)
Grant ID 10870415
Grant Description

PROJECT SUMMARY Title: Investigating spatial and temporal heterogeneity in mitochondria during aging using in vivo high- content chemical imaging The spatial and temporal regulation of mitochondria is critical for controlling various cellular processes, including energy balance and metabolism, in specific locations and timeframes. Mitochondria have the ability to dynami-

cally adjust their shape, position, activity, and interactions with other cellular components, such as lipid droplets (LDs), to fulfill the diverse functional requirements throughout an animal’s lifespan. However, the precise relation- ship between these spatial and temporal changes in mitochondria and the physiological homeostasis of host cells

and mitochondria is not fully understood. To address this question, we have developed advanced in vivo chemi- cal imaging techniques, specifically broadband coherent anti-Stokes Raman scattering (BCARS) and two-photon fluorescence lifetime imaging (2p-FLIM), and a genetically-tractable platform utilizing the nematode Caenorhab-

ditis elegans as the model organism. While BCARS and 2p-FLIM provide organelle-resolved data with very high information content associated with the metabolic states of subcellular compartments, the established in vivo platform offers the opportunity to examine various conditions. Our research aims to unravel the heterogeneity of

mitochondria in different physiological states, including their interactions with LDs, subcellular localization, and morphology in various tissues and cell types, and under different age and disease conditions within intact living animals. The successful completion of our proposed studies is expected to significantly advance our understand-

ing of the intricate relationship between physiological homeostasis and mitochondrial dynamics. Furthermore, the establishment of these novel imaging and analysis approaches will revolutionize the field of mitochondrial biology by providing a groundbreaking tool for reliably examining mitochondrial heterogeneity in vivo.

All Grantees

Georgia Institute of Technology

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