# Regulation of mitochondrial dynamics pathways in mammalian cells

> **NIH NIH R35** · UNIVERSITY OF COLORADO DENVER · 2024 · $383,699

## Abstract

PROJECT SUMMARY
 Mitochondria function is tightly regulated by a complex, intertwined machinery that dictates
mitochondrial gross morphology, transport of organelles, inner membrane and cristae morphology,
communication between adjacent mitochondria and contact with other organelles. These processes are
collectively known as mitochondrial dynamics. My overall goal is to reach a comprehensive understanding on
the mechanisms that govern mitochondrial dynamics and the interplay between mitochondrial transport with
other aspects of mitochondrial and cellular biology. While the mechanisms of mitochondrial transport had been
largely characterized in neurons, our recent advances showed that transport of energetically active
mitochondria to the cortical cytoskeleton supports lamellipodia dynamics, fuels turnover of focal adhesion
complexes and increases velocity and distance of random cell migration in epithelial cells. Because specialized
cell types have unique spatiotemporal needs for mitochondria functions, a fundamental question is how similar
are the mechanisms of mitochondrial movement between neurons and other cell types? Here we will focus on
characterizing the function and regulation of alternative isoforms of trafficking proteins that are expressed in
non-neuronal cells. Adding complexity to this picture, we have evidence of multifunctionality amongst trafficking
proteins in non-neuronal cells. These novel functions include mitochondrial metabolism and mitochondrial
signaling. This poses an important question: how are these multifunctional proteins regulated so single or
double functions are enabled at a particular time and location? Overall, my research program will lead to
discoveries on the regulation of mitochondrial trafficking and mitochondrial signaling pathways in non-neuronal
cells. Because mitochondria are key organelles that maintain cellular homeostasis, and mitochondrial
dysfunction are associated with neurological and metabolic diseases, cancer and aging, our advances have
the potential to inform how to exploit these mechanisms for practical applications in medicine.

## Key facts

- **NIH application ID:** 10834016
- **Project number:** 5R35GM142774-04
- **Recipient organization:** UNIVERSITY OF COLORADO DENVER
- **Principal Investigator:** Maria Cecilia Caino
- **Activity code:** R35 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $383,699
- **Award type:** 5
- **Project period:** 2021-06-15 → 2026-04-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10834016

## Citation

> US National Institutes of Health, RePORTER application 10834016, Regulation of mitochondrial dynamics pathways in mammalian cells (5R35GM142774-04). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10834016. Licensed CC0.

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