TY - JOUR
T1 - Single-cell microarray for analyzing cellular response
AU - Yamamura, Shohei
AU - Kishi, Hiroyuki
AU - Tokimitsu, Yoshiharu
AU - Kondo, Sachiko
AU - Honda, Ritsu
AU - Ramachandra Rao, Sathuluri
AU - Omori, Masahiro
AU - Tamiya, Eiichi
AU - Muraguchi, Atsushi
PY - 2005/12/15
Y1 - 2005/12/15
N2 - Detection of cellular response by measuring intracellular calcium, (Ca 2+) with Ca2+-dependent fluorescent dye are standard approaches to detect ligand-stimulated cells and to study signaling through ligand/receptor interaction. We describe a single-cell microarray system to analyze cellular response of individual cells such as lymphocytes using microchamber array chips. The single-cell microarray chip is made from polystyrene with over 30 000 microchambers, which can accommodate only single cells. Lymphocytes derived from mouse spleen or human blood were spread on the microarray, and over 80% of the microchambers achieved single-cell status. Stimulation of B-cells through antigen receptors on the microarray allowed us to detect activated B-cells by comparing the states of single B-cells before and after stimulation with antigen, which is disabled for flow cytometry. In addition, this novel method demonstrated retrieval of positive single B-cells from microchambers by a micromanipulator and achieved antibody DNA analysis. The system is suitable for high-throughput analysis of intracellular Ca 2+ response at the single-cell level and is applicable to screen antigen-specific lymphocytes for making specific monoclonal antibody.
AB - Detection of cellular response by measuring intracellular calcium, (Ca 2+) with Ca2+-dependent fluorescent dye are standard approaches to detect ligand-stimulated cells and to study signaling through ligand/receptor interaction. We describe a single-cell microarray system to analyze cellular response of individual cells such as lymphocytes using microchamber array chips. The single-cell microarray chip is made from polystyrene with over 30 000 microchambers, which can accommodate only single cells. Lymphocytes derived from mouse spleen or human blood were spread on the microarray, and over 80% of the microchambers achieved single-cell status. Stimulation of B-cells through antigen receptors on the microarray allowed us to detect activated B-cells by comparing the states of single B-cells before and after stimulation with antigen, which is disabled for flow cytometry. In addition, this novel method demonstrated retrieval of positive single B-cells from microchambers by a micromanipulator and achieved antibody DNA analysis. The system is suitable for high-throughput analysis of intracellular Ca 2+ response at the single-cell level and is applicable to screen antigen-specific lymphocytes for making specific monoclonal antibody.
UR - http://www.scopus.com/inward/record.url?scp=29244468315&partnerID=8YFLogxK
U2 - 10.1021/ac0515632
DO - 10.1021/ac0515632
M3 - 学術論文
C2 - 16351155
AN - SCOPUS:29244468315
SN - 0003-2700
VL - 77
SP - 8050
EP - 8056
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 24
ER -