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Publication : Shortening the thick filament by partial deletion of titin's C-zone alters cardiac function by reducing the operating sarcomere length range.

First Author  Methawasin M Year  2022
Journal  J Mol Cell Cardiol Volume  165
Pages  103-114 PubMed ID  35031281
Mgi Jnum  J:323323 Mgi Id  MGI:7262641
Doi  10.1016/j.yjmcc.2022.01.002 Citation  Methawasin M, et al. (2022) Shortening the thick filament by partial deletion of titin's C-zone alters cardiac function by reducing the operating sarcomere length range. J Mol Cell Cardiol 165:103-114
abstractText  Titin's C-zone is an inextensible segment in titin, comprised of 11 super-repeats and located in the cMyBP-C-containing region of the thick filament. Previously we showed that deletion of titin's super-repeats C1 and C2 (Ttn(DeltaC1-2) model) results in shorter thick filaments and contractile dysfunction of the left ventricular (LV) chamber but that unexpectedly LV diastolic stiffness is normal. Here we studied the contraction-relaxation kinetics from the time-varying elastance of the LV and intact cardiomyocyte, cellular work loops of intact cardiomyocytes, Ca(2+) transients, cross-bridge kinetics, and myofilament Ca(2+) sensitivity. Intact cardiomyocytes of Ttn(DeltaC1-2) mice exhibit systolic dysfunction and impaired relaxation. The time-varying elastance at both LV and single-cell levels showed that activation kinetics are normal in Ttn(DeltaC1-2) mice, but that relaxation is slower. The slowed relaxation is, in part, attributable to an increased myofilament Ca(2+) sensitivity and slower early Ca(2+) reuptake. Cross-bridge dynamics showed that cross-bridge kinetics are normal but that the number of force-generating cross-bridges is reduced. In vivo sarcomere length (SL) measurements revealed that in Ttn(DeltaC1-2) mice the operating SL range of the LV is shifted towards shorter lengths. This normalizes the apparent cell and LV diastolic stiffness but further reduces systolic force as systole occurs further down on the ascending limb of the force-SL relation. We propose that the reduced working SLs reflect titin's role in regulating diastolic stiffness by altering the number of sarcomeres in series. Overall, our study reveals that thick filament length regulation by titin's C-zone is critical for normal cardiac function.
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