Establishment of a CFTR-based detection method for the second messenger cAMP in the cytoplasm.
10.12047/j.cjap.6208.2022.015
- Author:
Ming-da WU
1
;
Xun-Ying LIU
2
;
Jian-Nan FENG
2
;
Xue-Wei GAO
2
;
Feng HAO
1
;
Jun-Tao GAO
3
Author Information
1. College of Laboratory Medicine, Jilin Medical College, Jilin 132013.
2. School of Medical Technology, Beihua University, Jilin 132013.
3. School of Basic Medicine, Jilin Medical College, Jilin 132013, China.
- Publication Type:Journal Article
- Keywords:
cAMP concentration;
cell model;
cystic fibrosis transmembrane conductance regulator;
second messenger
- MeSH:
Cyclic AMP;
Cystic Fibrosis Transmembrane Conductance Regulator;
Cytoplasm;
Second Messenger Systems
- From:
Chinese Journal of Applied Physiology
2022;38(1):79-84
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To establish a detection method based on Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) that can sensitively detect the second messenger cyclic AMP (cAMP) in the cytoplasm. Methods: The eukaryotic expression vectors of CFTR and YFP-H148Q / I152L were constructed respectively. FRT cells co-expressing CFTR and YFP-H148Q / I152L were obtained by liposome transfection. The expression of CFTR and YFP-H148Q / I152L in FRT cells was observed by an inverted fluorescence microscopy, and flow cytometry was used to detect the purity of cells; The cell model was identified by the fluorescence quenching kinetics test. The validation of the cell model which could screen CFTR modulators was verified by the fluorescence quenching kinetics experiments. The radioimmunoassay was used to detect the cAMP concentration in cytoplasm after adding CFTR activator. Results: The results of the inverted fluorescence microscope showed that CFTR was expressed in the cell membrane and YFP-H148Q / I152L was expressed in the cytoplasm of FRT cells. The FRT cell model stably co-expressing ANO1 and YFP-H148Q / I152L was successfully constructed. The model could screen CFTR modulators, and the slope of fluorescence change and the concentration of CFTR modulators were in a dose-dependent manner. The slope of the fluorescence could reflect the cAMP concentration in the cytoplasm. The cell model could sensitively detect the intracellular cAMP concentration. Conclusion: The cell model could efficiently and sensitively detect the second messenger cAMP concentration in the cytoplasm, and it provided a simple and efficient method for the study of other targets associated cAMP signal.
