Dennerll T J, Joshi H C, Steel V L, Buxbaum R E, Heidemann S R
Department of Physiology, Michigan State University, E. Lansing 48824.
J Cell Biol. 1988 Aug;107(2):665-74. doi: 10.1083/jcb.107.2.665.
We assessed the mechanical properties of PC-12 neurites by applying a force with calibrated glass needles and measured resulting changes in neurite length and deflection of the needle. We observed a linear relationship between force and length change that was not affected by multiple distensions and were thus able to determine neurite spring constants and initial, nondistended, rest tensions. 81 out of 82 neurites showed positive rest tensions ranging over three orders of magnitude with most values clustering around 30-40 mu dynes. Treatment with cytochalasin D significantly reduced neurite rest tensions to an average compression equal to 14% of the former tension and spring constants to an average of 17% of resting values. Treatment with nocodazole increased neurite rest tensions to an average of 282% of resting values but produced no change in spring constant. These observations suggest a particular type of complementary force interaction underlying axonal shape; the neurite actin network under tension and neurite microtubules under compression. Thermodynamics suggests that microtubule (MT) assembly may be regulated by changes in compressive load. We tested this effect by releasing neurite attachment to a polylysine-coated surface with polyaspartate, thus shifting external compressive support onto internal elements, and measuring the relative change in MT polymerization using quantitative Western blotting. Neurons grown on polylysine or collagen without further treatment had a 1:2 ratio of soluble to polymerized tubulin. When neurites grown on polylysine were treated with 1% polyaspartate for 15-30 min, 80% of neurites retracted, shifting the soluble: polymerized tubulin ratio to 1:1. Polyaspartate treatment of cells grown on collagen, or grown on polylysine but treated with cytochalasin to reduce tension, caused neither retraction nor a change in the soluble:polymerized tubulin ratio. We suggest that the release of adhesion to the dish shifted the compressive load formerly borne by the dish onto Mts causing their partial depolymerization. Our observations are consistent with the possibility that alterations in MT compression during growth cone advance integrates MT assembly with the advance.
我们通过用校准的玻璃针施加力来评估PC-12神经突的力学性能,并测量神经突长度的变化以及针的偏转。我们观察到力与长度变化之间呈线性关系,这种关系不受多次拉伸的影响,因此能够确定神经突的弹簧常数以及初始的、未拉伸的静止张力。82个神经突中有81个显示出正的静止张力,范围跨越三个数量级,大多数值集中在30 - 40微达因左右。用细胞松弛素D处理显著降低了神经突的静止张力,使其平均压缩力等于先前张力的14%,弹簧常数平均为静止值的17%。用诺考达唑处理使神经突静止张力增加到静止值的平均282%,但弹簧常数没有变化。这些观察结果表明轴突形状背后存在一种特殊类型的互补力相互作用;处于张力下的神经突肌动蛋白网络和处于压缩下的神经突微管。热力学表明微管(MT)组装可能受压缩负荷变化的调节。我们通过用聚天冬氨酸释放神经突与聚赖氨酸包被表面的附着来测试这种效应,从而将外部压缩支持转移到内部元件上,并使用定量蛋白质免疫印迹法测量MT聚合的相对变化。在聚赖氨酸或胶原蛋白上生长且未经进一步处理的神经元,其可溶性微管蛋白与聚合微管蛋白的比例为1:2。当在聚赖氨酸上生长的神经突用1%聚天冬氨酸处理15 - 30分钟时,80%的神经突回缩,使可溶性:聚合微管蛋白的比例变为1:1。用聚天冬氨酸处理在胶原蛋白上生长的细胞,或在聚赖氨酸上生长但用细胞松弛素处理以降低张力的细胞,既不会导致回缩,也不会使可溶性:聚合微管蛋白的比例发生变化。我们认为,与培养皿附着力的释放将先前由培养皿承担的压缩负荷转移到微管上,导致其部分解聚。我们的观察结果与生长锥前进过程中MT压缩的改变将MT组装与前进过程整合在一起的可能性一致。