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. Author manuscript; available in PMC: 2015 Jul 15.
Published in final edited form as: Arch Biochem Biophys. 2014 May 9;554:11–21. doi: 10.1016/j.abb.2014.04.017

Table 2. Force measurements in failing cardiomyocytes after exchange with recombinant cTn at sarcomere length 1.8 and 2.2 μm.

IDCM cardiomyocytes exchanged with Wt, 42D/44D and 42A/44A troponin complex (2 samples; 8 myocytes per complex). Myofilament force was measured at sarcomere lengths of 1.8 and 2.2 μm at different Ca2+-concentrations. Stretching of cardiomyocytes from 1.8 to 2.2 μm significantly increased Ca2+-sensitivity (pCa50), maximal (Fmax) and passive force (Fpas) in all groups. There was no significant effect of sarcomere length on nHill (steepness of the force-pCa curves). Two-way ANOVA repeated measures followed by a Bonferroni post-hoc test revealed a significant decrease in Ca2+-sensitivity in 42D/44D and 42A/44A compared to Wt at both sarcomere lengths (#P<0.05, significant difference compared to Wt). When two-way ANOVA revealed a significant effect for sarcomere length (P<0.05), paired t-tests were performed to compare cell measurements at two different sarcomere lengths in each cTn-exchange group (*P<0.05, 1.8 vs 2.2 μm). Wt data has been published before.23 Values are means ± SEM.

Wt 42D/44D 42A/44A

Fmax (kN.m−2) 1.8 μm 14.5±0.8 10.2±1.4 12.2±2.2
2.2 μm 18.0±1.0* 13.7±1.6* 15.1±2.0*

Fpas (kN.m−2) 1.8 μm 2.2±0.1 2.4±0.3 1.9±0.3
2.2 μm 3.3±0.3* 3.6±0.4* 3.1±0.5*

pCa50 1.8 μm 5.64±0.02 5.42±0.01# 5.56±0.02#
2.2 μm 5.67±0.02* 5.45±0.01#,* 5.60±0.02#,*

nHill 1.8 μm 2.9±0.1 2.4±0.2 2.5±0.2
2.2 μm 2.7±0.1 2.4±0.1 2.5±0.2