Mechanotransduction of cells under physical constraints

In this report, a direct quantitative way to measure the mechanotransduction of cells under physical constraints was discussed. This was accomplished by both microcontact printing and cell traction force microscopy study. A flexible polyacrylamide (PAL) gel embedded with fluorescent microbeads wa...

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Bibliographic Details
Main Author: Low, Agnes Fang Ting.
Other Authors: Chan Vincent
Format: Final Year Project (FYP)
Language:English
Published: 2009
Subjects:
Online Access:http://hdl.handle.net/10356/16448
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author Low, Agnes Fang Ting.
author2 Chan Vincent
author_facet Chan Vincent
Low, Agnes Fang Ting.
author_sort Low, Agnes Fang Ting.
collection NTU
description In this report, a direct quantitative way to measure the mechanotransduction of cells under physical constraints was discussed. This was accomplished by both microcontact printing and cell traction force microscopy study. A flexible polyacrylamide (PAL) gel embedded with fluorescent microbeads was polymerized on an activated glass surface. Adhesive islands were created on the surface of the gel or directly on activated glass surfaces by microcontact printing. Rat aorta cells were cultured on these islands. The cells spread to take on the shape and size of the islands. Cell traction force was then quantified by mapping displacement fields of the fluorescent microbeads within the micron-sized adhesive islands of defined shape and size. The results drew the relationship between cell traction force and various cell shapes.
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spelling ntu-10356/164482023-03-03T15:31:47Z Mechanotransduction of cells under physical constraints Low, Agnes Fang Ting. Chan Vincent School of Chemical and Biomedical Engineering DRNTU::Engineering::Chemical engineering::Biotechnology In this report, a direct quantitative way to measure the mechanotransduction of cells under physical constraints was discussed. This was accomplished by both microcontact printing and cell traction force microscopy study. A flexible polyacrylamide (PAL) gel embedded with fluorescent microbeads was polymerized on an activated glass surface. Adhesive islands were created on the surface of the gel or directly on activated glass surfaces by microcontact printing. Rat aorta cells were cultured on these islands. The cells spread to take on the shape and size of the islands. Cell traction force was then quantified by mapping displacement fields of the fluorescent microbeads within the micron-sized adhesive islands of defined shape and size. The results drew the relationship between cell traction force and various cell shapes. Bachelor of Engineering (Chemical and Biomolecular Engineering) 2009-05-26T06:13:50Z 2009-05-26T06:13:50Z 2009 2009 Final Year Project (FYP) http://hdl.handle.net/10356/16448 en Nanyang Technological University 42 p. application/pdf
spellingShingle DRNTU::Engineering::Chemical engineering::Biotechnology
Low, Agnes Fang Ting.
Mechanotransduction of cells under physical constraints
title Mechanotransduction of cells under physical constraints
title_full Mechanotransduction of cells under physical constraints
title_fullStr Mechanotransduction of cells under physical constraints
title_full_unstemmed Mechanotransduction of cells under physical constraints
title_short Mechanotransduction of cells under physical constraints
title_sort mechanotransduction of cells under physical constraints
topic DRNTU::Engineering::Chemical engineering::Biotechnology
url http://hdl.handle.net/10356/16448
work_keys_str_mv AT lowagnesfangting mechanotransductionofcellsunderphysicalconstraints