دورية أكاديمية

The Multitarget Ligand 3-Iodothyronamine Modulates β-Adrenergic Receptor 2 Signaling.

التفاصيل البيبلوغرافية
العنوان: The Multitarget Ligand 3-Iodothyronamine Modulates β-Adrenergic Receptor 2 Signaling.
المؤلفون: Dinter J; Institut für Experimentelle Pädiatrische Endokrinologie, Berlin, Germany., Khajavi N; Department of Ophthalmology, Charité-Universitätsmedizin Berlin, Berlin, Germany., Mühlhaus J; Institut für Experimentelle Pädiatrische Endokrinologie, Berlin, Germany., Wienchol CL; Institut für Experimentelle Pädiatrische Endokrinologie, Berlin, Germany., Cöster M; Institut für Biochemie, Molekulare Biochemie, Medizinische Fakultät, University of Leipzig, Leipzig, Germany., Hermsdorf T; Institut für Biochemie, Molekulare Biochemie, Medizinische Fakultät, University of Leipzig, Leipzig, Germany., Stäubert C; Institut für Biochemie, Molekulare Biochemie, Medizinische Fakultät, University of Leipzig, Leipzig, Germany., Köhrle J; Institut für Experimentelle Endokrinologie, Charité-Universitätsmedizin Berlin, Berlin, Germany., Schöneberg T; Institut für Biochemie, Molekulare Biochemie, Medizinische Fakultät, University of Leipzig, Leipzig, Germany., Kleinau G; Institut für Experimentelle Pädiatrische Endokrinologie, Berlin, Germany., Mergler S; Department of Ophthalmology, Charité-Universitätsmedizin Berlin, Berlin, Germany., Biebermann H; Institut für Experimentelle Pädiatrische Endokrinologie, Berlin, Germany.
المصدر: European thyroid journal [Eur Thyroid J] 2015 Sep; Vol. 4 (Suppl 1), pp. 21-9. Date of Electronic Publication: 2015 May 29.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Bioscientifica Ltd Country of Publication: England NLM ID: 101604579 Publication Model: Print-Electronic Cited Medium: Print ISSN: 2235-0640 (Print) Linking ISSN: 22350640 NLM ISO Abbreviation: Eur Thyroid J Subsets: PubMed not MEDLINE
أسماء مطبوعة: Publication: 2022- : [Bristol] : Bioscientifica Ltd.
Original Publication: Basel : S. Karger
مستخلص: Background: 3-Iodothyronamine (3-T1AM), a signaling molecule with structural similarities to thyroid hormones, induces numerous physiological responses including reversible body temperature decline. One target of 3-T1AM is the trace amine-associated receptor 1 (TAAR1), which is a member of the rhodopsin-like family of G protein-coupled receptors (GPCRs). Interestingly, the effects of 3-T1AM remain detectable in TAAR1 knockout mice, suggesting further targets for 3-T1AM such as adrenergic receptors. Therefore, we evaluated whether β-adrenergic receptor 1 (ADRB1) and 2 (ADRB2) signaling is affected by 3-T1AM in HEK293 cells and in human conjunctival epithelial cells (IOBA-NHC), where these receptors are highly expressed endogenously.
Methods: A label-free EPIC system for prescreening the 3-T1AM-induced effects on ADRB1 and ADRB2 in transfected HEK293 cells was used. In addition, ADRB1 and ADRB2 activation was analyzed using a cyclic AMP assay and a MAPK reporter gene assay. Finally, fluorescence Ca(2+) imaging was utilized to delineate 3-T1AM-induced Ca(2+) signaling.
Results: 3-T1AM (10(-5)-10(-10)M) enhanced isoprenaline-induced ADRB2-mediated Gs signaling but not that of ADRB1-mediated signaling. MAPK signaling remained unaffected for both receptors. In IOBA-NHC cells, norepinephrine-induced Ca(2+) influxes were blocked by the nonselective ADRB blocker timolol (10 µM), indicating that ADRBs are most likely linked with Ca(2+) channels. Notably, timolol was also found to block 3-T1AM (10(-5)M)-induced Ca(2+) influx.
Conclusions: The presented data support that 3-T1AM directly modulates β-adrenergic receptor signaling. The relationship between 3-T1AM and β-adrenergic signaling also reveals a potential therapeutic value for suppressing Ca(2+) channel-mediated inflammation processes, occurring in eye diseases such as conjunctivitis.
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فهرسة مساهمة: Keywords: Calcium channel; Calcium homeostasis; Human conjunctiva; Signaling; Thyronamine; β-Adrenergic receptors
تواريخ الأحداث: Date Created: 20151125 Date Completed: 20151125 Latest Revision: 20200930
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC4640289
DOI: 10.1159/000381801
PMID: 26601070
قاعدة البيانات: MEDLINE
الوصف
تدمد:2235-0640
DOI:10.1159/000381801