During development, tissues are sculpted into organs with precise forms and functions in a process called tissue morphogenesis. Tissue morphogenesis results from cellular forces that are transmitted across the tissue. Improper generation or coordination of forces leads to defects in organ formation, such as neural tube defects. Abnormal activation of pathways that generate cellular forces and drive cell shape change can promote cancer cell metastasis. Therefore, it is critical to both our understanding of development and human disease to determine the mechanisms that control tissue morphogenesis at the molecular, cellular, and tissue level. Tissue invagination during gastrulation and neural tube closure is driven by apical constriction of epithelial cells. This causes columnar cells to adopt a wedge shape, which promotes folding of the epithelial sheet. We made the surprising discovery that apical constriction during Drosophila gastrulation is driven by pulsed contractions and subsequent stabilization of the actin-myosin cytoskeleton. Contraction pulses have now been observed to promote many different morphogenetic processes, including tissue contraction, convergent extension, and axis elongation. The molecular mechanisms responsible for this dynamic contraction and how contractile force is transmitted and coordinated across the tissue is unknown. The availability of live imaging, quantitative image analysis, genetics (mutants, RNAi), cell biology (drugs), biophysics (laser cutting), and biochemistry makes Drosophila gastrulation a powerful system to address these questions. We will investigate how forces propagate from the molecular to the tissue level. First, we will determine the function of myosin motor activity and actin filament depolymerization during pulsatile contraction. Second, we will examine how contractile forces are transmitted between cells to generate epithelial tension. Third, we will determine how biochemical and mechanical signals regulate the coordination of cell shape across the tissue and whether pulsation is critical for this coordination. This multidisciplinary and multiscale approach is essential to understand how dynamic molecular and cellular behaviors collectively result in precise changes in tissue morphology. Members of my lab have backgrounds in cell biology, genetics, physics, and computer science. In addition, we have established collaborations with computational biophysicists and a functional genomics lab to expand our research capabilities. We are poised to make important discoveries regarding the molecular and cellular mechanisms that drive tissue morphogenesis.

Public Health Relevance

Understanding mechanisms of tissue morphogenesis is fundamental to understanding birth defects and cancer progression. We will undertake a multidisciplinary approach to examine how mechanical forces are generated and transmitted between cells to sculpt tissues during development. These studies promise to provide insight into how molecular and cellular behaviors are regulated and coordinated during development.

Agency
National Institute of Health (NIH)
Type
Research Project (R01)
Project #
5R01GM105984-02
Application #
8645656
Study Section
Development - 2 Study Section (DEV2)
Program Officer
Hoodbhoy, Tanya
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02142
Vasquez, Claudia G; Tworoger, Mike; Martin, Adam C (2014) Dynamic myosin phosphorylation regulates contractile pulses and tissue integrity during epithelial morphogenesis. J Cell Biol 206:435-50
Chanet, Soline; Martin, Adam C (2014) Mechanical force sensing in tissues. Prog Mol Biol Transl Sci 126:317-52