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光镊揭示阻碍表面活性物质胞吐释放的机械力。

Mechanical forces impeding exocytotic surfactant release revealed by optical tweezers.

作者信息

Singer Wolfgang, Frick Manfred, Haller Thomas, Bernet Stefan, Ritsch-Marte Monika, Dietl Paul

机构信息

Department of Medical Physics, University of Innsbruck, A-6020 Innsbruck, Austria.

出版信息

Biophys J. 2003 Feb;84(2 Pt 1):1344-51. doi: 10.1016/S0006-3495(03)74950-9.

Abstract

The release of surfactant from alveolar type II cells is essential to lower the surface tension in the lung and to facilitate inspiration. However, the factors controlling dispersal and diffusion of this hydrophobic material are still poorly understood. Here we report that release of surfactant from the fused vesicle, termed lamellar body (LB), resisted mechanical forces applied by optical tweezers: At constant trapping force, the probability to expand LB contents, i.e., to "pull" surfactant into the extracellular fluid, increased with time after LB fusion with the plasma membrane, consistent with slow fusion pore expansion in these cells. Elevations of the cytoplasmic Ca(2+) concentration (Ca(2+)) had a similar effect. Inasmuch as surfactant did not disintegrate in the extracellular space, this method permitted for the first time the determination of elastic and recoil properties of the macromolecular complex, yielding a spring constant of approximately 12.5 pN/ micro m. This is the first functional evidence that release of hydrophobic material is mechanically impeded and occurs in an "all-or-none" fashion. This mode of release is most probably the result of cohesive forces of surfactant, combined with adhesive forces and/or retaining forces exerted by a constrictive fusion pore acting as a regulated mechanical barrier, withstanding forces up to 160 pN. In independent experiments equiaxial strain was exerted on cells without optical tweezers. Strain facilitated surfactant release from preexisting fused vesicles, consistent with the view of mechanical impediments during the release process, which can be overcome by cell strain.

摘要

肺泡II型细胞释放表面活性剂对于降低肺表面张力和促进吸气至关重要。然而,控制这种疏水性物质分散和扩散的因素仍知之甚少。在此我们报告,从融合小泡(称为板层小体,LB)释放表面活性剂可抵抗光镊施加的机械力:在恒定捕获力下,LB内容物扩张的概率,即“拉”表面活性剂进入细胞外液的概率,在LB与质膜融合后的时间里增加,这与这些细胞中融合孔缓慢扩张一致。细胞质Ca(2+)浓度([Ca(2+)]c)升高有类似作用。由于表面活性剂在细胞外空间不会分解,这种方法首次允许测定大分子复合物的弹性和回缩特性,得出的弹簧常数约为12.5 pN/μm。这是第一个功能性证据,表明疏水性物质的释放受到机械阻碍且以“全或无”方式发生。这种释放模式很可能是表面活性剂内聚力、结合力和/或由作为调节性机械屏障的收缩性融合孔施加的保留力共同作用的结果,该融合孔能承受高达160 pN的力。在独立实验中,在没有光镊的情况下对细胞施加等轴应变。应变促进了表面活性剂从预先存在的融合小泡中释放,这与释放过程中存在机械阻碍的观点一致,而这种阻碍可通过细胞应变克服。

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