Regulation and function of region-specific tissue mechanical properties in epithelial folding

NIH RePORTER · NIH · R35 · $409,328 · view on reporter.nih.gov ↗

Abstract

During embryogenesis, the formation of complex tissues and organs are usually driven by remodeling of epithelial cells. Epithelial morphogenesis is an intrinsically mechanical process dictated by forces and the mechanical properties of tissues. Despite significant progress in deciphering the genetic and biochemical determinants of force generation, little is known about how tissue mechanical properties are regulated and how this regulation contributes to morphogenesis. Using Drosophila gastrulation as a model, our recent work reveals that the collective cell shape changes underlying apical constriction-mediated mesoderm invagination are dictated by region-specific mechanical properties of the tissue. The tissue interior behaves as a viscous continuum and flows as the cells constrict apically, thereby mediating the apical- basal lengthening of the cells. In contrast, the subsequent tissue invagination is contingent on the rigidity of the apical surface of the flanking, non-constricting cells. The mechanical properties inherent to the tissue interior and surface are controlled by proteins that regulate cell membrane expansion and cell polarity, respectively. Disruption of these proteins affects specific aspects of tissue folding. In the proposed study, we will use a multipronged approach combining genetics, quantitative live-imaging, biophysics and computer modeling to (1) identify the cellular mechanisms that facilitate viscous deformation of cells in the tissue interior and (2) determine how the rigidity of the tissue surface is regulated and how flanking cells contribute to tissue invagination. To facilitate our work, we have developed biophysical approaches to probe tissue mechanical properties in vivo and optogenetic tools to control protein activities with high spatiotemporal precision. Successful completion of our research goals will advance scientific knowledge by identifying cellular mechanisms that define region-specific mechanical properties and pinpointing their role in coherent tissue deformation. Moreover, our findings will shed light on the fundamental regulatory networks that govern how tissues sense and respond to mechanical forces underlying a variety of developmental and physiological processes.

Key facts

NIH application ID
10439448
Project number
5R35GM128745-05
Recipient
DARTMOUTH COLLEGE
Principal Investigator
Bing He
Activity code
R35
Funding institute
NIH
Fiscal year
2022
Award amount
$409,328
Award type
5
Project period
2018-07-20 → 2024-12-31