Functional Expression of KATP Channel on Human Periodontal Ligament Cells
Objectives: Adenosine-5’-triphosphate (ATP) has been mentioned in dental research on multiple levels, such as inflammation, mechanical strain and pain, making the system particularly relevant for the specific challenges in the oral cavity. There are studies showing human periodontal ligament (PDL) cells respond to mechanical stress by increasing ATP release, which participates in bone resorption or bone homeostasis. Methods: In this study, we used the RT-PCR and patch-clamp technique to investigate the presence of KATP channel subunits and influence of ATP on the KATP channel opening on PDL cells. Results: We observed transcripts for Kir6.1, Kir6.2 and Sur2B mRNAs isolated from the human PDL cells. In inside-out patch mode, the single channel conductance was 163 pS at symmetrical K+ concentration of 140 mM and inward rectification was seen at the ATP-free bath solution. The reversal potential of the currents was found to be 0 mV at symmetrical concentration (140 mM) of K+ in bath solution. The single channel currents were almost blocked by adding 5 mM ATP in the bath solution. However, the currents were not blocked by 100 μM glibenclamide, a subunit specific KATP channel blocker. Conclusions: These results indicate that human PDL cells express KATP channels which are not sensitive to glibenclamide. This research was supported by Basic Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2014R1A1A2054241) and (2015R1D1A3A01018700)
Division: IADR/APR General Session
Meeting:2016 IADR/APR General Session (Seoul, Korea) Location: Seoul, Korea
Year: 2016 Final Presentation ID:0759 Abstract Category|Abstract Category(s):Periodontal Research-Therapy
Authors
Tran, Phuong
( Chonbuk National University
, Jeon-ju
, Korea (the Republic of)
)
Park, Soo-joung
( Chonbuk National University
, Jeon-ju
, Korea (the Republic of)
)
Han, Seong-kyu
( Chonbuk National University
, Jeon-ju
, Korea (the Republic of)
)
Support Funding Agency/Grant Number: This research was supported by Basic Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2014R1A1A2054241) and (2015R1D1A3A01018700)
Financial Interest Disclosure: NONE