James R. DePauw Professor of Physiology, Dept. of Cell and Molecular Physiology, Loyola Univ. Chicago, 2160 South First Ave., Stritch School of Medicine, Maywood, IL, 60153-5500, USA.
Am J Physiol Heart Circ Physiol. 2011 Jun;300(6):H2155-60. doi: 10.1152/ajpheart.01221.2010. Epub 2011 Apr 1.
The cellular mechanism underlying the Frank-Starling law of the heart is myofilament length-dependent activation. The mechanism(s) whereby sarcomeres detect changes in length and translate this into increased sensitivity to activating calcium has been elusive. Small-angle X-ray diffraction studies have revealed that the intact myofilament lattice undergoes numerous structural changes upon an increase in sarcomere length (SL): lattice spacing and the I(1,1)/I(1,0) intensity ratio decreases, whereas the M3 meridional reflection intensity (I(M3)) increases, concomitant with increases in diastolic and systolic force. Using a short (∼10 ms) X-ray exposure just before electrical stimulation, we were able to obtain detailed structural information regarding the effects of external osmotic compression (with mannitol) and obtain SL on thin intact electrically stimulated isolated rat right ventricular trabeculae. We show that over the same incremental increases in SL, the relative changes in systolic force track more closely to the relative changes in myosin head orientation (as reported by I(M3)) than to the relative changes in lattice spacing. We conclude that myosin head orientation before activation determines myocardial sarcomere activation levels and that this may be the dominant mechanism for length-dependent activation.
心肌的 Frank-Starling 定律的细胞机制是肌丝长度依赖性激活。肌节检测长度变化并将其转化为对激活钙敏感性增加的机制一直难以捉摸。小角 X 射线衍射研究表明,完整的肌丝晶格在肌节长度增加时会发生许多结构变化:晶格间距和 I(1,1)/I(1,0) 强度比降低,而 M3 子午线反射强度 (I(M3)) 增加,同时舒张和收缩力增加。我们使用短(约 10 毫秒)X 射线照射,在电刺激之前,可以获得关于外部渗透压(甘露醇)的影响以及在薄的完整电刺激的分离的大鼠右心室小梁上获得肌节长度的详细结构信息。我们表明,在相同的肌节长度递增中,收缩力的相对变化与肌球蛋白头部取向的相对变化(如 I(M3) 所报道)更密切相关,而不是与晶格间距的相对变化更密切相关。我们得出结论,激活前肌球蛋白头部取向决定心肌肌节的激活水平,这可能是长度依赖性激活的主要机制。