TY - JOUR
T1 - Analysis of single-cell differences by use of an on-chip microculture system and optical trapping
AU - Wakamoto, Yuichi
AU - Inoue, Ippei
AU - Moriguchi, Hiroyuki
AU - Yasuda, Kenji
N1 - Funding Information:
Acknowledgments We thank Dr K. Kaneko of the University of Tokyo and Dr T. Yomo of Osaka University for their valuable advice and for stimulating discussions. This study was supported in part by Grants-in-Aids for Science Research from the Ministry of Education, Science and Culture of Japan (No. 11CE2006 (Komaba Complex Systems Life Science Project) to Dr. Kaneko, and No. 12206028 to KY).
PY - 2001
Y1 - 2001
N2 - A method is described for continuous observation of isolated single cells that enables genetically identical cells to be compared; it uses an on-chip microculture system and optical tweezers. Photolithography is used to construct microchambers with 5-μm-high walls made of thick photoresist (SU-8) on the surface of a glass slide. These microchambers are connected by a channel through which cells are transported, by means of optical tweezers, from a cultivation microchamber to an analysis microchamber, or from the analysis microchamber to a waste microchamber. The microchambers are covered with a semi-permeable membrane to separate them from nutrient medium circulating through a "cover chamber" above. Differential analysis of isolated direct descendants of single cells showed that this system could be used to compare genetically identical cells under contamination-free conditions. It should thus help in the clarification of heterogeneous phenomena, for example unequal cell division and cell differentiation.
AB - A method is described for continuous observation of isolated single cells that enables genetically identical cells to be compared; it uses an on-chip microculture system and optical tweezers. Photolithography is used to construct microchambers with 5-μm-high walls made of thick photoresist (SU-8) on the surface of a glass slide. These microchambers are connected by a channel through which cells are transported, by means of optical tweezers, from a cultivation microchamber to an analysis microchamber, or from the analysis microchamber to a waste microchamber. The microchambers are covered with a semi-permeable membrane to separate them from nutrient medium circulating through a "cover chamber" above. Differential analysis of isolated direct descendants of single cells showed that this system could be used to compare genetically identical cells under contamination-free conditions. It should thus help in the clarification of heterogeneous phenomena, for example unequal cell division and cell differentiation.
UR - http://www.scopus.com/inward/record.url?scp=0034828108&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034828108&partnerID=8YFLogxK
U2 - 10.1007/s002160100999
DO - 10.1007/s002160100999
M3 - Article
C2 - 11678202
AN - SCOPUS:0034828108
SN - 1618-2642
VL - 371
SP - 276
EP - 281
JO - Analytical and Bioanalytical Chemistry
JF - Analytical and Bioanalytical Chemistry
IS - 2
ER -