Department of Biomedicine, University of Bergen, Jonas-Lies vei 91, 5009, Bergen, Norway.
Cell Mol Neurobiol. 2010 Apr;30(3):369-79. doi: 10.1007/s10571-009-9459-2. Epub 2009 Sep 29.
Axonal transport of peptide and hormone-containing large dense core vesicles (LDCVs) is known to be a microtubule-dependent process. Here, we suggest a role for the actin-based motor protein myosin Va specifically in retrograde axonal transport of LDCVs. Using live-cell imaging of transfected hippocampal neurons grown in culture, we measured the speed, transport direction, and the number of LDCVs that were labeled with ectopically expressed neuropeptide Y fused to EGFP. Upon expression of a dominant-negative tail construct of myosin Va, a general reduction of movement in both dendrites and axons was observed. In axons, it was particularly interesting that the retrograde speed of LDCVs was significantly impaired, although anterograde transport remained unchanged. Moreover, particles labeled with the dominant-negative construct often moved in the retrograde direction but rarely in the anterograde direction. We suggest a model where myosin Va acts as an actin-dependent vesicle motor that facilitates retrograde axonal transport.
肽类和含有激素的大致密核心囊泡(LDCV)的轴突运输已知是微管依赖性的过程。在这里,我们提出肌球蛋白 Va 作为一种肌球蛋白马达蛋白,它在 LDCV 的逆行轴突运输中起作用。通过对培养的转染海马神经元的活细胞成像,我们测量了用外源性表达的与 EGFP 融合的神经肽 Y 标记的 LDCV 的速度、运输方向和数量。在表达肌球蛋白 Va 的显性负性尾部构建体后,观察到树突和轴突中的运动都普遍减少。在轴突中,特别有趣的是 LDCV 的逆行速度明显受损,尽管顺行运输保持不变。此外,用显性负性构建体标记的颗粒通常以逆行方向移动,但很少以顺行方向移动。我们提出了一个模型,其中肌球蛋白 Va 作为一种肌球蛋白马达蛋白,作为一种依赖于肌动蛋白的囊泡马达,促进逆行轴突运输。