Home > Publications database > TRPV1 activation and internalization is part of the LPS-induced inflammation in human iPSC-derived cardiomyocytes. > print |
001 | 169897 | ||
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041 | _ | _ | |a English |
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100 | 1 | _ | |a Sattler, Katherine |b 0 |
245 | _ | _ | |a TRPV1 activation and internalization is part of the LPS-induced inflammation in human iPSC-derived cardiomyocytes. |
260 | _ | _ | |a [London] |c 2021 |b Macmillan Publishers Limited, part of Springer Nature |
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520 | _ | _ | |a The non-selective cation channel transient receptor potential vanilloid 1 (TRPV1) is expressed throughout the cardiovascular system. Recent evidence shows a role for TRPV1 in inflammatory processes. The role of TRPV1 for myocardial inflammation has not been established yet. Human induced pluripotent stem cell (iPSC)-derived cardiomyocytes (hiPSC-CM) from 4 healthy donors were incubated with lipopolysaccharides (LPS, 6 h), TRPV1 agonist capsaicin (CAP, 20 min) or the antagonist capsazepine (CPZ, 20 min). TRPV1 expression was studied by PCR and western blotting. TRPV1 internalization was analyzed by immunofluorescence. Interleukin-6 (IL-6) secretion and phosphorylation of JNK, p38 and ERK were determined by ELISA. TRPV1-associated ion channel current was measured by patch clamp. TRPV1-mRNA and -protein were expressed in hiPSC-CM. TRPV1 was localized in the plasma membrane. LPS significantly increased secretion of IL-6 by 2.3-fold, which was prevented by pre-incubation with CPZ. LPS induced TRPV1 internalization. Phosphorylation levels of ERK, p38 or JNK were not altered by TRPV1 stimulation or inhibition. LPS and IL-6 significantly lowered TRPV1-mediated ion channel current. TRPV1 mediates the LPS-induced inflammation in cardiomyocytes, associated with changes of cellular electrophysiology. LPS-induced inflammation results in TRPV1 internalization. Further studies have to examine the underlying pathways and the clinical relevance of these findings. |
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700 | 1 | _ | |a El-Battrawy, Ibrahim |b 1 |
700 | 1 | _ | |a Cyganek, Lukas |0 0000-0001-9120-1382 |b 2 |
700 | 1 | _ | |a Lang, Siegfried |b 3 |
700 | 1 | _ | |a Lan, Huan |b 4 |
700 | 1 | _ | |a Li, Xin |0 P:(DE-He78)128e4949aa4cb04fe109c52df0c67732 |b 5 |u dkfz |
700 | 1 | _ | |a Zhao, Zhihan |b 6 |
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700 | 1 | _ | |a Wieland, Thomas |b 8 |
700 | 1 | _ | |a Borggrefe, Martin |b 9 |
700 | 1 | _ | |a Zhou, Xiaobo |b 10 |
700 | 1 | _ | |a Akin, Ibrahim |b 11 |
773 | _ | _ | |a 10.1038/s41598-021-93958-3 |g Vol. 11, no. 1, p. 14689 |0 PERI:(DE-600)2615211-3 |n 1 |p 14689 |t Scientific reports |v 11 |y 2021 |x 2045-2322 |
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