# Investigating mechanisms regulating cytoskeletal dynamics and alignment during epithelial tissue folding > **NIH NIH F32** · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · 2021 · $65,994 ## Abstract Project Summary: Large-scale tissue movements are critical during development to transform an amorphous collection of cells into organs with specific structure and function. Abnormal activation of force-generating signals that regulate epithelial morphogenesis can result in developmental defects, such as neural tube deformities, as well as aberrant epithelial-mesenchymal transition and cancer metastasis. Yet we do not fully understand how mechanical forces generated at the molecular level regulate epithelial remodeling. At the cellular level, most forces are generated by the actomyosin network; the molecular motor non-muscle myosin II (myosin) crosslinks actin filaments (F-actin), thereby generating contractile forces which are propagated throughout the tissue via intercellular connections. One outcome of actomyosin contractility is apical contraction, in which the apex of the cell narrows as a result of repeated bursts of myosin pulses that condense the F-actin cortex in a ratchet-like manner. When myosin pulsing and ratcheting is disrupted, cells fail to apically constrict and the tissue fails to fold. However, the mechanisms driving pulsatile contractions and ratcheting behavior remains poorly understood, highlighting a critical gap in our understanding of how upstream signaling events are intricately linked to downstream changes in cytoskeletal organization and behavior. The long-term goal of this project is to determine how mechanical forces generated at the molecular level collectively drive tissue-wide morphogenetic changes. The overall objective of this proposal is to identify mechanisms that regulate myosin dynamics and alignment by determining the mechanistic link between Twist expression and myosin turnover. The rationale for this proposed work is to gain insight not only into the nature of these mechanisms, but also the general principles governing contractility and ratchet-like apical constriction during large-scale tissue movements. Our central hypothesis is that Twist, and its downstream effectors, as well as tissue-wide forces, via intercellular connections, cooperatively regulate myosin dynamics to drive apical ratcheting and tissue remodeling events during embryonic development in Drosophila. This hypothesis will be tested by pursuing two specific aims: we will (1) determine the mechanism through which Twist promotes cell apex stabilization, and (2) determine how myosin dynamics are affected by intercellular connectivity. Our approach is innovative because it is one of the first to directly examine myosin dynamics using an integrative strategy that combines classic Drosophila genetics with advanced microscopy methods, including photo-conversion and super- resolution imaging. The proposed research is significant because it will advance our understanding of the connection between gene expression, signaling pathways, and force production during epithelial morphogenesis, and will provide new perspective to ongoing research efforts ... ## Key facts - **NIH application ID:** 10229158 - **Project number:** 1F32GM142152-01 - **Recipient organization:** MASSACHUSETTS INSTITUTE OF TECHNOLOGY - **Principal Investigator:** Mary Ann Collins - **Activity code:** F32 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2021 - **Award amount:** $65,994 - **Award type:** 1 - **Project period:** 2021-04-01 → 2024-03-31 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/10229158 ## Citation > US National Institutes of Health, RePORTER application 10229158, Investigating mechanisms regulating cytoskeletal dynamics and alignment during epithelial tissue folding (1F32GM142152-01). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10229158. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*