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논문 기본 정보

자료유형
학위논문
저자정보

송지영 (서울대학교, 서울대학교 대학원)

발행연도
2016
저작권
서울대학교 논문은 저작권에 의해 보호받습니다.

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이 논문의 연구 히스토리 (2)

초록· 키워드

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Significant advances in micro technology has been made to study cellular behavior, but there is still absence of robust profile generating device for mammalian cells. Unlike the unicellular organism, mammalian cell needs longer period of stimulation at least 6 hours more. Moreover, previous research revealed the limitation of petri-dish based conventional experiment. Since the cells are exposed to “dynamic environment” rather than static, conventional method can’t represent our real world. There has been lots of studies to generate versatile gradient for long-time, but the stimulation time is too short to employ to mammalian cells. In addition to this point, we could only generate one type of profile such as pulsing, gradient. Here we propose the microfluidic device that can generate all kinds of user defined profiles sequentially through computer controlled system. With this versatile device, we could generate pulsatile, ramping up/down, various gradient switching for long time.
Moreover, recent study discovered heterogeneous behavior of single cells, which has never stood out before with average-based analysis. Based on the result, the single cells exhibit heterogeneity in ERK activation under the EGF or NGF stimulation. In this thesis, when the cells exposed to EGF gradient, some of the cells showed sustained activation. In contrast, the others behaved like the stimulation without any growth factors. It implies the cells might be switched on when they reached their threshold. Moreover, we observed that decay of activation was also delayed. Further studies are needed to determine what exactly affect this phenomena and rewire the signaling molecules. However, this work is still meaningful in the aspect of building long term multi-functional microfluidic platform. We expect this novel device to be used to study dynamic stimulation and their related cellular response in diverse filed of biology.

목차

1. Introduction 7
1.1 Microfluidic in Cell Biology 7
1.2 Spatiotemporal dynamic stimulation and ERK signaling network 10
2. Methods and Materials 16
2.1 Generation of FRET biosensor transfected cell-line and culture 16
2.2 Design of microfluidic device 17
2.3 Fabrication of microfluidic device 19
2.4 Soft lithography and Device preparation 22
2.5 Cell seeding 25
2.6 Live cell Imaging 26
2.7 Image analysis 28
3. Result and Discussion 29
3.1 Ramping up and down profiles 29
3.2 Gradient switching profiles and Single cell ERK activation 33
4. Conclusion 36
References 37
Abstract (Korean) 39

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