Award Abstract # 2145756
CAREER: Biomechanics of Leader Cells

NSF Org: CMMI
Division of Civil, Mechanical, and Manufacturing Innovation
Recipient: VIRGINIA COMMONWEALTH UNIVERSITY
Initial Amendment Date: January 4, 2022
Latest Amendment Date: June 3, 2022
Award Number: 2145756
Award Instrument: Continuing Grant
Program Manager: Shivani Sharma
shisharm@nsf.gov
 (703)292-4204
CMMI
 Division of Civil, Mechanical, and Manufacturing Innovation
ENG
 Directorate for Engineering
Start Date: February 1, 2022
End Date: January 31, 2027 (Estimated)
Total Intended Award Amount: $562,255.00
Total Awarded Amount to Date: $578,255.00
Funds Obligated to Date: FY 2022 = $578,255.00
History of Investigator:
  • Priscilla Hwang (Principal Investigator)
    hwangp2@vcu.edu
Recipient Sponsored Research Office: Virginia Commonwealth University
910 WEST FRANKLIN ST
RICHMOND
VA  US  23284-9005
(804)828-6772
Sponsor Congressional District: 04
Primary Place of Performance: Virginia Commonwealth University
P.O. Box 980568
RICHMOND
VA  US  23298-0568
Primary Place of Performance
Congressional District:
04
Unique Entity Identifier (UEI): MLQFL4JSSAA9
Parent UEI: WXQLZ1PA6XP3
NSF Program(s): CAREER: FACULTY EARLY CAR DEV,
BMMB-Biomech & Mechanobiology
Primary Program Source: 01002223DB NSF RESEARCH & RELATED ACTIVIT
01002324DB NSF RESEARCH & RELATED ACTIVIT

010V2122DB R&RA ARP Act DEFC V
Program Reference Code(s): 070Z, 1045, 116E, 9102, 9178, 9179, 9231, 9251
Program Element Code(s): 104500, 747900
Award Agency Code: 4900
Fund Agency Code: 4900
Assistance Listing Number(s): 47.041

ABSTRACT

This award is funded in whole or in part under the American Rescue Plan Act of 2021 (Public Law 117-2).

This Faculty Early Career Development (CAREER) award will support research to investigate the migration of groups of cells, specifically, how mechanical forces from the external environment and cellular mechanical forces guide migration. The migration of groups of cells is necessary for development of many tissues. However, migration can also be a sign of development abnormalities or disease advancement. For cells to move together, a unique sub-set of cells, those called the leader cells, must move to the front. The leader cells receive signals from their surroundings and send signals to other cells in the group so they can all move together. However, how leader cells are uniquely able to carry out these functions is still largely unknown. This research will begin to unravel how leader cells sense, interpret, and send mechanical signals. This will provide a more comprehensive understanding of how groups of cells move together. This research will be complemented by an educational program to recruit and retain diverse populations of students in STEM. Underrepresented minorities, women, and first-generation students will be engaged through research, mentoring, and course development for high school, undergraduate and graduate students. Work will also be conducted with K-12 teachers in Virginia using inquiry-based science lessons. The activities will promote STEM awareness to K-12 students using hands-on experiments based on research findings.

The specific goal of this research is to understand how leader cells, biomechanical extracellular matrix (ECM) cues, and cellular mechanics are intertwined to influence the migration of clusters of cells in a process known as collective migration. The central hypothesis is that leader cells polarize to the leading edge through increased protrusive adhesions biased in the direction of the biomechanical cue, interstitial fluid flow, and cellular generated forces required to sustain directed collective migration. Using a novel, in vitro, 3D microphysiological system that can replicate dynamic ECM cues and incorporate cell clusters to model and induce collective migration, this research will investigate: 1) how leader cells polarize from within a collective unit to the front in the direction of interstitial fluid flow, and 2) if leader cells are mechanically connected and how mechanical forces between leader cells initiate and sustain collective migration. Understanding how leader cells function and lead to collective migration will not only expand our understanding of collective migration driven developmental processes, but also provide a new perspective for therapy design addressing development abnormalities or disease progression where leader cell driven collective migration has gone awry.

This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH

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Lichtenberg, Jessanne_Y and Leonard, Corinne_E and Sterling, Hazel_R and Santos_Agreda, Valentina and Hwang, Priscilla_Y "Using Microfluidics to Align Matrix Architecture and Generate Chemokine Gradients Promotes Directional Branching in a Model of Epithelial Morphogenesis" ACS Biomaterials Science & Engineering , v.10 , 2024 https://doi.org/10.1021/acsbiomaterials.4c00245 Citation Details
Lichtenberg, Jessanne Y. and Ramamurthy, Ella and Young, Anna D. and Redman, Trey P. and Leonard, Corinne E. and Das, Swadesh K. and Fisher, Paul B. and Lemmon, Christopher A. and Hwang, Priscilla Y. "Leader cells mechanically respond to aligned collagen architecture to direct collective migration" PLOS ONE , v.19 , 2024 https://doi.org/10.1371/journal.pone.0296153 Citation Details

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