Award Abstract # 1647837
Nanosystems Engineering Research Center for Directed Multiscale Assembly of Cellular Metamaterials with Nanoscale Precision: CELL-MET

NSF Org: EEC
Div Of Engineering Education and Centers
Recipient: TRUSTEES OF BOSTON UNIVERSITY
Initial Amendment Date: September 8, 2017
Latest Amendment Date: September 20, 2023
Award Number: 1647837
Award Instrument: Cooperative Agreement
Program Manager: Randy Duran
rduran@nsf.gov
 (703)292-5326
EEC
 Div Of Engineering Education and Centers
ENG
 Directorate For Engineering
Start Date: October 1, 2017
End Date: September 30, 2027 (Estimated)
Total Intended Award Amount: $19,750,000.00
Total Awarded Amount to Date: $32,524,446.00
Funds Obligated to Date: FY 2017 = $3,500,000.00
FY 2018 = $7,587,511.00

FY 2019 = $950,561.00

FY 2020 = $5,154,126.00

FY 2021 = $4,368,248.00

FY 2022 = $7,640,481.00

FY 2023 = $3,219,519.00
History of Investigator:
  • David Bishop (Principal Investigator)
    djb1@bu.edu
  • Christopher Chen (Co-Principal Investigator)
  • Arvind Agarwal (Co-Principal Investigator)
  • Alice White (Co-Principal Investigator)
  • Brendon Baker (Co-Principal Investigator)
  • Stephen Forrest (Former Co-Principal Investigator)
Recipient Sponsored Research Office: Trustees of Boston University
1 SILBER WAY
BOSTON
MA  US  02215-1703
(617)353-4365
Sponsor Congressional District: 07
Primary Place of Performance: Trustees of Boston University
MA  US  02215-1300
Primary Place of Performance
Congressional District:
07
Unique Entity Identifier (UEI): THL6A6JLE1S7
Parent UEI:
NSF Program(s): RES EXP FOR TEACHERS(RET)-SITE,
ERC-Eng Research Centers
Primary Program Source: 01002223DB NSF RESEARCH & RELATED ACTIVIT
01002324DB NSF RESEARCH & RELATED ACTIVIT

01001718DB NSF RESEARCH & RELATED ACTIVIT

01001819DB NSF RESEARCH & RELATED ACTIVIT

01001920DB NSF RESEARCH & RELATED ACTIVIT

01002021DB NSF RESEARCH & RELATED ACTIVIT

01002122DB NSF RESEARCH & RELATED ACTIVIT
Program Reference Code(s): 102Z, 113E, 115E, 116E, 123E, 124E, 129E, 131E, 1480, 7218, 7633, 7680, 9177, 9178
Program Element Code(s): 135900, 148000
Award Agency Code: 4900
Fund Agency Code: 4900
Assistance Listing Number(s): 47.041

ABSTRACT

Heart disease is the number one cause of death in the US and a leading cause worldwide, but current medicine cannot regenerate and or repair diseased human heart tissue. Today, there is no cure for a heart attack. The vision of Directed Multiscale Assembly of Cellular Metamaterials with Nanoscale Precision (CELL-MET) Nanosystems Engineering Research Center is to change this. CELL-MET will develop tissue-engineering principles to create scalable, low-cost technologies for growing clinically significant cardiac tissues from cell-level building blocks. The research approach is to adapt and advance novel nanomanufacturing techniques to integrate a variety of functional biological structures and elements into flexible polymer scaffolds that support and guide heart cells. The goal of this project is to create cardiac patches that will someday allow for the repair of hearts damaged by a heart attack or other diseases. In addition to their potential for repairing damaged hearts, artificial cardiac tissues will be used to test the effects of heart drugs or other drugs more realistically and efficiently than is currently possible. Broader impacts will include kindergarten to post-doctoral education and training programs that will produce a diverse, well-trained, world aware workforce to support the new billion dollar industries enabled by CELL-MET research. Industrial partners will work with CELL-MET to create these new industries, developing the business opportunities generated by the research breakthroughs.

CELL-MET aims to create functional, clinically significant heart tissue in the laboratory by controlling the cardiac structure across different length scales. At sizes smaller than a micron and up to the ten micron scale of cells, CELL-MET will align heart muscle cells (cardiomyocytes) and connect them to one another via special cellular structures, enabling them to contract and relax in synchrony. At the multicellular scale, it will monitor and control chemical signaling both among these cells and between them and supporting cells. At the scale of tissue constructs, CELL-MET will create highly structured networks of blood vessels lined with epithelial cells, which are needed for any thick tissue. The ten-year vision encompasses the incorporation of endocardial cells that help define the large-scale structure and electrophysiological function of the heart, as well as the valves that ensure unidirectional blood flow.
CELL-MET brings together a diverse, world-class team from Boston University, the University of Michigan, Florida International University, Harvard, Columbia, Argonne National Lab, EPFL (Switzerland), and Centro Atomico-Bariloche (Argentina). The team has expertice in semiconductors, photonics, nanotechnology, optical systems, organic molecules, cardiac biology, and cellular assembly. CELL-MET is uniquely positioned to harness the capabilities and synergies among these disciplines. CELL-MET plans to combine novel techniques for patterning molecules on the scale of 50 nm or less with nanometer resolution 3D-printed scaffolds. 3D nanoprinting technologies will produce scaffolds that Atomic Calligraphy and Organic Vapor Jet Printing will write upon to create the focal adhesion points, the places that attach the cells. Advanced tissue engineering techniques will populate these nanostructures with cardiomyocytes and other cardiac cell types to produce the living tissues.
As CELL-MET advances the technology, it will work with commercial members of its Innovation Ecosystem to create entirely new industries. Through its Education and Workforce Development programs, CELL-MET will recruit and train a diverse, world aware workforce to support the industries that it creates.

PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH

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Stange, Alexander and Imboden, Matthias and Javor, Josh and Barrett, Lawrence K. and Bishop, David J. "Building a Casimir metrology platform with a commercial MEMS sensor" Microsystems & Nanoengineering , v.5 , 2019 10.1038/s41378-019-0054-5 Citation Details
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Reeves, Jeremy B. and Jayne, Rachael K. and Barrett, Lawrence and White, Alice E. and Bishop, David J. "Fabrication of multi-material 3D structures by the integration of direct laser writing and MEMS stencil patterning" Nanoscale , v.11 , 2019 10.1039/C8NR09174A Citation Details
Zhu, Xuena and Sarwar, Mehenur and Zhu, Jun-Jie and Zhang, Chengxiao and Kaushik, Ajeet and Li, Chen-Zhong "Using a glucose meter to quantitatively detect disease biomarkers through a universal nanozyme integrated lateral fluidic sensing platform" Biosensors and Bioelectronics , v.126 , 2019 10.1016/j.bios.2018.11.033 Citation Details
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Lu, Wenjing and Jiao, Yuan and Gao, Yifang and Qiao, Jie and Mozneb, Maedeh and Shuang, Shaomin and Dong, Chuan and Li, Chen-zhong "Bright Yellow Fluorescent Carbon Dots as a Multifunctional Sensing Platform for the Label-Free Detection of Fluoroquinolones and Histidine" ACS Applied Materials & Interfaces , v.10 , 2018 10.1021/acsami.8b16710 Citation Details
Venkidasubramonian, Gowthamy and Kratzer, Domenic and Trouillet, Vanessa and Zydziak, Nicolas and Franzreb, Matthias and Barner, Leonie and Lahann, Joerg "Surface-initiated RAFT polymerization from vapor-based polymer coatings" Polymer , v.150 , 2018 10.1016/j.polymer.2018.06.073 Citation Details
(Showing: 1 - 10 of 93)

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