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1.
Heart Vessels ; 36(7): 1027-1034, 2021 Jul.
Article in English | MEDLINE | ID: mdl-33507357

ABSTRACT

Reported mapping procedures of left atrial (LA) low-voltage areas (LVAs) vary widely. This study aimed to compare the PentaRay®/CARTO®3 (PentaRay map) and Orion™/Rhythmia™ (Orion map) systems for LA voltage mapping. This study included 15 patients who underwent successful pulmonary vein isolation (PVI) for atrial fibrillation. After PVI, PentaRay and Orion maps created for all patients were compared. LVAs were defined as sites with ≥ 3 adjacent low-voltage points < 0.5 mV. LVAs were indicated in 8 (53%) among 15 patients, and the average values of the measured LVAs was comparable between the systems (PentaRay map = 5.4 ± 8.7 cm2; Orion map = 4.3 ± 6.4 cm2, p = 0.69). However, in 2 of 8 patients with LVAs, the Orion map indicated LVAs at the septum and posterolateral sites of the LA, respectively, whereas the PentaRay map indicated no LVAs. In those patients, sharp electrograms of > 0.5 mV were properly recorded at the septum and posterolateral sites during appropriate beats in the PentaRay map. The PentaRay map had a shorter procedure time than the Orion map (12 ± 3 min vs. 23 ± 8 min, respectively; p < 0.01). Our study results showed a discrepancy in the LVA evaluation between the PentaRay and Orion maps. In 2 of 15 patients, the Orion map indicated LVAs at the sites where > 0.5-mV electrograms were properly recorded in the PentaRay map.


Subject(s)
Atrial Fibrillation/physiopathology , Atrial Function, Left/physiology , Body Surface Potential Mapping/methods , Heart Atria/physiopathology , Action Potentials , Aged , Aged, 80 and over , Atrial Fibrillation/diagnosis , Atrial Fibrillation/surgery , Catheter Ablation/methods , Cryosurgery/methods , Female , Humans , Male , Middle Aged , Pulmonary Veins/surgery
2.
J Biol Chem ; 289(36): 24801-9, 2014 Sep 05.
Article in English | MEDLINE | ID: mdl-25059661

ABSTRACT

Cyanobacteria have unique photoreceptors, cyanobacteriochromes, that show diverse spectral properties to sense near-UV/visible lights. Certain cyanobacteriochromes have been shown to regulate cellular phototaxis or chromatic acclimation of photosynthetic pigments. Some cyanobacteriochromes have output domains involved in bacterial signaling using a second messenger cyclic dimeric GMP (c-di-GMP), but its role in cyanobacteria remains elusive. Here, we characterize the recombinant Tlr0924 from a thermophilic cyanobacterium Thermosynechococcus elongatus, which was expressed in a cyanobacterial system. The protein reversibly photoconverts between blue- and green-absorbing forms, which is consistent with the protein prepared from Escherichia coli, and has diguanylate cyclase activity, which is enhanced 38-fold by blue light compared with green light. Therefore, Tlr0924 is a blue light-activated diguanylate cyclase. The protein's relatively low affinity (10.5 mM) for Mg(2+), which is essential for diguanylate cyclase activity, suggests that Mg(2+) might also regulate c-di-GMP signaling. Finally, we show that blue light irradiation under low temperature is responsible for Thermosynechococcus vulcanus cell aggregation, which is abolished when tlr0924 is disrupted, suggesting that Tlr0924 mediates blue light-induced cell aggregation by producing c-di-GMP. Given our results, we propose the name "sesA (sessility-A)" for tlr0924. This is the first report for cyanobacteriochrome-dependent regulation of a sessile/planktonic lifestyle in cyanobacteria via c-di-GMP.


Subject(s)
Bacterial Proteins/metabolism , Cyanobacteria/metabolism , Escherichia coli Proteins/metabolism , Phosphorus-Oxygen Lyases/metabolism , Photoreceptors, Microbial/metabolism , Bacterial Proteins/genetics , Binding, Competitive , Cyanobacteria/cytology , Cyanobacteria/genetics , Cyclic GMP/analogs & derivatives , Cyclic GMP/metabolism , Electrophoresis, Polyacrylamide Gel , Enzyme Activation/radiation effects , Escherichia coli/genetics , Escherichia coli Proteins/genetics , Light , Magnesium/metabolism , Magnesium/pharmacology , Models, Biological , Mutation , Phosphorus-Oxygen Lyases/genetics , Photoreceptors, Microbial/genetics , Protein Binding , Recombinant Proteins/metabolism , Signal Transduction/drug effects , Spectrophotometry , Temperature
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