Role of the acidic N′ region of cardiac troponin I in regulating myocardial function
| العنوان: | Role of the acidic N′ region of cardiac troponin I in regulating myocardial function |
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| المؤلفون: | Natosha L. Finley, Hanna Osinska, Jeffrey Robbins, Paul R. Rosevear, Raisa Klevitsky, Sakthivel Sadayappan, Jack W. Howarth, John N. Lorenz |
| المصدر: | The FASEB Journal. 22:1246-1257 |
| بيانات النشر: | Wiley, 2007. |
| سنة النشر: | 2007 |
| مصطلحات موضوعية: | Gene isoform, medicine.medical_specialty, Contraction (grammar), Molecular Sequence Data, chemistry.chemical_element, Mice, Transgenic, Stimulation, macromolecular substances, Calcium, Biochemistry, Article, Contractility, Mice, Internal medicine, Troponin I, Genetics, medicine, Animals, Humans, Magnesium, Myocytes, Cardiac, Amino Acid Sequence, Phosphorylation, Molecular Biology, Adenosine Triphosphatases, Myocardium, Heart, musculoskeletal system, Endocrinology, chemistry, cardiovascular system, PRKCE, Biotechnology |
| الوصف: | Cardiac troponin I (cTnI) phosphorylation modulates myocardial contractility and relaxation during beta-adrenergic stimulation. cTnI differs from the skeletal isoform in that it has a cardiac specific N' extension of 32 residues (N' extension). The role of the acidic N' region in modulating cardiac contractility has not been fully defined. To test the hypothesis that the acidic N' region of cTnI helps regulate myocardial function, we generated cardiac-specific transgenic mice in which residues 2-11 (cTnI(Delta2-11)) were deleted. The hearts displayed significantly decreased contraction and relaxation under basal and beta-adrenergic stress compared to nontransgenic hearts, with a reduction in maximal Ca(2+)-dependent force and maximal Ca(2+)-activated Mg(2+)-ATPase activity. However, Ca(2+) sensitivity of force development and cTnI-Ser(23/24) phosphorylation were not affected. Chemical shift mapping shows that both cTnI and cTnI(Delta2-11) interact with the N lobe of cardiac troponin C (cTnC) and that phosphorylation at Ser(23/24) weakens these interactions. These observations suggest that residues 2-11 of cTnI, comprising the acidic N' region, do not play a direct role in the calcium-induced transition in the cardiac regulatory or N lobe of cTnC. We hypothesized that phosphorylation at Ser(23/24) induces a large conformational change positioning the conserved acidic N region to compete with actin for the inhibitory region of cTnI. Consistent with this hypothesis, deletion of the conserved acidic N' region results in a decrease in myocardial contractility in the cTnI(Delta2-11) mice demonstrating the importance of acidic N' region in regulating myocardial contractility and mediating the response of the heart to beta-AR stimulation. |
| تدمد: | 1530-6860 0892-6638 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f7a37c824d960f481e31904facacf2eTest https://doi.org/10.1096/fj.07-9458comTest |
| حقوق: | OPEN |
| رقم الانضمام: | edsair.doi.dedup.....5f7a37c824d960f481e31904facacf2e |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 15306860 08926638 |
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