Principles of Mechanochemical Signal Integration Underlying Developmental Robustness

NIH RePORTER · NIH · R35 · $372,100 · view on reporter.nih.gov ↗

Abstract

Project Summary / Abstract My research program aims to understand cellular mechanisms underlying robust embryonic tissue patterning. Despite environmental fluctuations, tissues develop nearly identical patterns, shapes, and sizes among different stage-matched individuals. In contrast, artificial tissues grown in vitro are highly variable, limiting their value for disease modeling. How single cells can reliably sense and control tissue parameters remains an important open question in both developmental biology and tissue engineering. Departing from the traditional focus of patterning control by biochemical signaling, my research aims to understand how cells integrate biochemical and mechanical signals to detect and respond to changes in tissue pattern and shape. We are empowered by our expertise in in vivo live imaging, zebrafish genetics, computational modeling, and innovative approaches to manipulating tissues’ biochemical and mechanical environments. Using these multidisciplinary tools, we will test how cells incorporate mechanical information to detect tissue-scale changes that are challenging to detect by morphogen signaling alone. First, we will determine whether cells can sense the cell type identity of their neighbors through cadherin-based adhesion, and use this information to modify cell fate decisions and correct errors in tissue patterning. Second, we will identify mechano-responsive morphogen signaling pathways and investigate whether mechanochemical crosstalk allows the cells to infer their relative positions more accurately in tissues undergoing morphogenesis. By revealing how tissue parameters are encoded by biochemical and mechanical signals, and how cells decode mechanochemical signals to sense and control changes in tissue parameters, our research will elucidate the information flow from tissue-scale changes to cellular responses. Our work will establish cell adhesion and mechanical force as key channels of tissue information directing accurate cellular decisions in early tissue patterning events, a novel paradigm that will impact our understanding of development, mechanical consequences in diseases, and engineering strategies for artificial tissues.

Key facts

NIH application ID
10932878
Project number
5R35GM150759-02
Recipient
WASHINGTON UNIVERSITY
Principal Investigator
Tony Yu-Chen Tsai
Activity code
R35
Funding institute
NIH
Fiscal year
2024
Award amount
$372,100
Award type
5
Project period
2023-09-22 → 2028-08-31