TY - JOUR
T1 - Intensive Immunofluorescence Staining Methods for Low Expression Protein
T2 - Detection of Intestinal Stem Cell Marker LGR5
AU - Yamazaki, Masaki
AU - Kato, Atsuhiko
AU - Zaitsu, Yoko
AU - Watanabe, Takeshi
AU - Iimori, Makoto
AU - Funahashi, Shinichi
AU - Kitao, Hiroyuki
AU - Saeki, Hiroshi
AU - Oki, Eiji
AU - Suzuki, Masami
PY - 2015/10/29
Y1 - 2015/10/29
N2 - Leucine-rich repeat-containing G-protein coupled receptor 5, or LGR5, is a molecule that recognizes stem cells in multiple organs and also in colon cancer. Previously, we have developed monoclonal antibodies specific to LGR5 protein that can be used for immunofluorescence staining, but because a very low level of LGR5 protein is expressed, the visualization technique needed to be enhanced. To develop procedures to detect LGR5 protein in various specimens by immunofluorescence staining, we evaluated the Alexa-labeled streptavidin biotin (LSAB), the Qdot, and the tyramide methods. The detection sensitivity was highest in the tyramide method followed by the Qdot method, whereas subcellular localization of the protein was most clear in the Qdot method, because the Qdot method gave a high S/N ratio that could show a low background. Thus, the tyramide method is superior to the Q-dot method for intensifying the signal of a low expression protein, and the Qdot method is superior to the tyramide method for identifying the subcellular localization of the target protein. The results of the present study will be helpful in providing more insight into the pathophysiological roles of LGR5-positive cancer stem cells and in developing therapeutic approaches for targeting cancer stem cells.
AB - Leucine-rich repeat-containing G-protein coupled receptor 5, or LGR5, is a molecule that recognizes stem cells in multiple organs and also in colon cancer. Previously, we have developed monoclonal antibodies specific to LGR5 protein that can be used for immunofluorescence staining, but because a very low level of LGR5 protein is expressed, the visualization technique needed to be enhanced. To develop procedures to detect LGR5 protein in various specimens by immunofluorescence staining, we evaluated the Alexa-labeled streptavidin biotin (LSAB), the Qdot, and the tyramide methods. The detection sensitivity was highest in the tyramide method followed by the Qdot method, whereas subcellular localization of the protein was most clear in the Qdot method, because the Qdot method gave a high S/N ratio that could show a low background. Thus, the tyramide method is superior to the Q-dot method for intensifying the signal of a low expression protein, and the Qdot method is superior to the tyramide method for identifying the subcellular localization of the target protein. The results of the present study will be helpful in providing more insight into the pathophysiological roles of LGR5-positive cancer stem cells and in developing therapeutic approaches for targeting cancer stem cells.
U2 - 10.1267/ahc.15019
DO - 10.1267/ahc.15019
M3 - Article
C2 - 26633908
SN - 0044-5991
VL - 48
SP - 159
EP - 164
JO - Acta Histochemica et Cytochemica
JF - Acta Histochemica et Cytochemica
IS - 5
ER -