Analyzing the morphology of 3T3 fibroblasts in microenvironment
碩士 === 國立臺灣大學 === 物理研究所 === 99 === We have created 3D ordered gelatin scaffolds with monodisperse pores and cultured 3T3 fibroblasts inside. We are interested to explore the effect of microenvironment on the cell morphologies. The morphologies of cells are observed through labeling the F-actin insid...
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ndltd-TW-099NTU051980092015-10-28T04:07:30Z http://ndltd.ncl.edu.tw/handle/09911122804363365317 Analyzing the morphology of 3T3 fibroblasts in microenvironment 探討3T3纖維母細胞在三維微環境中的形狀 Wei-Hong Hong 洪瑋嶸 碩士 國立臺灣大學 物理研究所 99 We have created 3D ordered gelatin scaffolds with monodisperse pores and cultured 3T3 fibroblasts inside. We are interested to explore the effect of microenvironment on the cell morphologies. The morphologies of cells are observed through labeling the F-actin inside the cells with fluorescent phalloidin and imaged by a confocal microscope. To segment the cell properly, we first reduced the autofluorescence background from the scaffold by changing the crosslinking chemistry. We compared the cell morphologies in the following microenvironment - on a 2D hard surface, on a 2D soft gelatin surface, in a 3D collagen gel, and scaffolds of different pore sizes. We found that the cells exhibit wide range of morphologies in different microenvironment. We classified cell shapes into three categories and measured the extension of cells by fitting with an ellipsoid. From the trend of cell extensions, a cell in a large pore resembles one on 2D soft gel surface. This result suggests a crossover in length from 2D-like to 3D-like morphology for cell cultured on a curved surface. 陳義裕 2010 學位論文 ; thesis 21 en_US |
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碩士 === 國立臺灣大學 === 物理研究所 === 99 === We have created 3D ordered gelatin scaffolds with monodisperse pores and cultured 3T3 fibroblasts inside. We are interested to explore the effect of microenvironment on the cell morphologies. The morphologies of cells are observed through labeling the F-actin inside the cells with fluorescent phalloidin and imaged by a confocal microscope. To segment the cell properly, we first reduced the autofluorescence background from the scaffold by changing the crosslinking chemistry. We compared the cell morphologies in the following microenvironment - on a 2D hard surface, on a 2D soft gelatin surface, in a 3D collagen gel, and scaffolds of different pore sizes. We found that the cells exhibit wide range of morphologies in different microenvironment. We classified cell shapes into three categories and measured the extension of cells by fitting with an ellipsoid. From the trend of cell extensions, a cell in a large pore resembles one on 2D soft gel surface. This result suggests a crossover in length from 2D-like to 3D-like morphology for cell cultured on a curved surface.
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陳義裕 |
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陳義裕 Wei-Hong Hong 洪瑋嶸 |
author |
Wei-Hong Hong 洪瑋嶸 |
spellingShingle |
Wei-Hong Hong 洪瑋嶸 Analyzing the morphology of 3T3 fibroblasts in microenvironment |
author_sort |
Wei-Hong Hong |
title |
Analyzing the morphology of 3T3 fibroblasts in microenvironment |
title_short |
Analyzing the morphology of 3T3 fibroblasts in microenvironment |
title_full |
Analyzing the morphology of 3T3 fibroblasts in microenvironment |
title_fullStr |
Analyzing the morphology of 3T3 fibroblasts in microenvironment |
title_full_unstemmed |
Analyzing the morphology of 3T3 fibroblasts in microenvironment |
title_sort |
analyzing the morphology of 3t3 fibroblasts in microenvironment |
publishDate |
2010 |
url |
http://ndltd.ncl.edu.tw/handle/09911122804363365317 |
work_keys_str_mv |
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1718114046095392768 |