Award Abstract # 1942003
CAREER: Light-sheet Brillouin microscopy for mechanical analysis of tissue morphogenesis

NSF Org: DBI
Division of Biological Infrastructure
Recipient: UNIVERSITY OF MARYLAND, COLLEGE PARK
Initial Amendment Date: March 23, 2020
Latest Amendment Date: March 23, 2020
Award Number: 1942003
Award Instrument: Standard Grant
Program Manager: Eric Lyons
erlyons@nsf.gov
 (703)292-0000
DBI
 Division of Biological Infrastructure
BIO
 Directorate for Biological Sciences
Start Date: July 1, 2020
End Date: June 30, 2025 (Estimated)
Total Intended Award Amount: $537,623.00
Total Awarded Amount to Date: $537,623.00
Funds Obligated to Date: FY 2020 = $537,623.00
History of Investigator:
  • giuliano scarcelli (Principal Investigator)
    scarc@umd.edu
Recipient Sponsored Research Office: University of Maryland, College Park
3112 LEE BUILDING
COLLEGE PARK
MD  US  20742-5100
(301)405-6269
Sponsor Congressional District: 04
Primary Place of Performance: University of Maryland
4228 A. James Clark Hall
College Park
MD  US  20742-0001
Primary Place of Performance
Congressional District:
04
Unique Entity Identifier (UEI): NPU8ULVAAS23
Parent UEI: NPU8ULVAAS23
NSF Program(s): Infrastructure Innovation for,
Animal Developmental Mechanism
Primary Program Source: 01002021DB NSF RESEARCH & RELATED ACTIVIT
Program Reference Code(s): 1045
Program Element Code(s): 084Y00, 111900
Award Agency Code: 4900
Fund Agency Code: 4900
Assistance Listing Number(s): 47.074

ABSTRACT

An award is made to the University of Maryland to develop a novel imaging technology, light-sheet Brillouin microscopy, to measure how biological cells grow into complex tissues during embryonic development. While previous technologies have mostly focused on probing genetic and biochemical control of tissue growth, this research will improve the understanding the biomechanical aspect of embryonic development. The project will generate a new instrument whose performance and design will be disseminated via conferences, peer-reviewed journal papers as well as hosting interested biological researchers. The project, at the interface of photonics, biomechanics and developmental biology, will provide opportunities to educate and train graduate and undergraduate students with a diverse set of skills. The project will also be used to attract middle-school students to STEM fields with activities relying on hands-on exercises that create quick connections between photonic technology and real-life familiar applications.

While our understanding of genetic, biochemical and molecular controls of tissue growth can rely on several established methods, the biomechanics of tissue morphogenesis remains poorly understood mostly due to the lack of suitable measurement techniques. This project addresses this need by developing light-sheet Brillouin microscopy capable of mapping elastic modulus in a developing embryo without contact at high 3D resolution. Brillouin microscopy has already proven impactful in tissue and cell biomechanics, but currently relies on point-scanning to build an image and thus is not suited for embryo studies due to speed and damage limitations. This project will develop massively multiplexed Brillouin spectral analysis and integrate it in widely used light-sheet microscopy platforms, which already provide structural and functional imaging, thus enabling mechanobiology studies of morphogenesis with co-localization of elasticity information, cell/tissue size, shape and organization as well as signaling activation and expression patterns. Co-Funding for this award is also being provided by the BIO/IOS-Developmental Systems Cluster.

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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Hutchins, Romanus and Zanini, Giulia and Scarcelli, Giuliano "Full-field optical spectroscopy at a high spectral resolution using atomic vapors" Optics Express , v.31 , 2023 https://doi.org/10.1364/OE.479253 Citation Details

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