- 영문명
- Measurement of Cellular ATP Efflux by Establishment of Biosensor Cells
- 발행기관
- 대한약학회
- 저자명
- 손민정(Min-Jeong Son) 레안위(Qui Ahn Le) 김준철(Joon-Chul Kim) 김경희(Kyoung-Hee Kim) 우선희(Sun-Hee Woo)
- 간행물 정보
- 『약학회지』제63권 제1호(2019년), 30~36쪽, 전체 7쪽
- 주제분류
- 의약학 > 기타의약학
- 파일형태
- 발행일자
- 2019.01.30

국문 초록
영문 초록
In this study, we established a biosensor cell that can directly respond to ATP in order to measure ATP release
from a single cell in real-time with high time resolution. We made HEK293 cells overexpressing P2X7 purinoceptors, the ATP-gated cation channel, with green fluorescence proteins (GFPs). Overexpression of P2X7 receptors was confirmed by reverse transcription-polymerase chain reaction, immunoblotting method, and fluorescence microscopy. In addition, the overexpression of P2X7 receptors was functionally confirmed by measuring ATP-induced cation current in these cells using whole-cell patch clamp technique. Application of ATP-containing external solutions produced inward currents at −70 mV in P2X7-expressing HEK293 cells, in a concentration-dependent manner with an EC50 of 31.2 μM. Maximal P2X7 inward current (14.2 ± 1.76 pA/pF, n = 10) was observed at about 0.8 mM ATP. ATP-dependent HEK293 cell currents were almost completely blocked by suramin (30 μM), the P2 purinergic antagonist (0.17 ± 0.13 pA/pF, n = 10, p < 0.0001), and they were negligible in the HEK293 cells expressing GFP only (0.28 ± 0.07 pA/pF, n = 11). The ATP-biosensor cells successfully detected ATP release from single atrial myocyte under shear stress at millisecond intervals. This ATP detection method may be used to directly quantify real-time ATP release, which may provide improved spatial and temporal information on cellular ATP release.
목차
서 론(Introduction)
실험방법(Experimental Methods)
결과 및 고찰(Results and Discussion)
결 론(Conclusion)
감사의 말씀(Acknowledgment)
References
해당간행물 수록 논문
참고문헌
최근 이용한 논문
교보eBook 첫 방문을 환영 합니다!
신규가입 혜택 지급이 완료 되었습니다.
바로 사용 가능한 교보e캐시 1,000원 (유효기간 7일)
지금 바로 교보eBook의 다양한 콘텐츠를 이용해 보세요!
