Mechanical forces impeding exocytotic surfactant release revealed by optical tweezers.

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+)](c)) 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.

[1]  Wolfgang Singer,et al.  Three-dimensional force calibration of optical tweezers , 2000 .

[2]  J. M. Fernández,et al.  Atomic force microscopy study of the secretory granule lumen. , 1996, Biophysical journal.

[3]  M. Lindau,et al.  Fusion pore expansion in horse eosinophils is modulated by Ca2+ and protein kinase C via distinct mechanisms , 1998, The EMBO journal.

[4]  Julio M Fernandez,et al.  Release of secretory products during transient vesicle fusion , 1993 .

[5]  P. Munson,et al.  Exocytotic fusion pores exhibit semi-stable states , 1993, The Journal of Membrane Biology.

[6]  W. Almers,et al.  Role of actin cortex in the subplasmalemmal transport of secretory granules in PC-12 cells. , 2000, Biophysical journal.

[7]  Y. Miyashita,et al.  Sequential-replenishment mechanism of exocytosis in pancreatic acini , 2001, Nature Cell Biology.

[8]  J. M. Fernández,et al.  Kinetics of release of serotonin from isolated secretory granules. I. Amperometric detection of serotonin from electroporated granules. , 1997, Biophysical journal.

[9]  Arthur Ashkin,et al.  Optical Trapping and Manipulation of Neutral Particles Using Lasers , 1999 .

[10]  G. Alvarez de Toledo,et al.  The exocytotic event in chromaffin cells revealed by patch amperometry , 1997, Nature.

[11]  B. Suki,et al.  Alveolar epithelial surface area-volume relationship in isolated rat lungs , 1999 .

[12]  K. Svoboda,et al.  Biological applications of optical forces. , 1994, Annual review of biophysics and biomolecular structure.

[13]  T. Haller,et al.  Dynamics of surfactant release in alveolar type II cells. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[14]  E. Tsilibary,et al.  Actin and secretion of surfactant. , 1983, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[15]  J. Gil Histological preservation and ultrastructure of alveolar surfactant. , 1985, Annual review of physiology.

[16]  H. Wirtz,et al.  Calcium mobilization and exocytosis after one mechanical stretch of lung epithelial cells. , 1990, Science.

[17]  K. Schütze,et al.  Force generation of organelle transport measured in vivo by an infrared laser trap , 1990, Nature.

[18]  E. Neher Secretion without full fusion , 1993, Nature.

[19]  Robert H. Chow,et al.  Delay in vesicle fusion revealed by electrochemical monitoring of single secretory events in adrenal chromaffin cells , 1992, Nature.

[20]  M. Frick,et al.  Fusion pore expansion is a slow, discontinuous, and Ca2+-dependent process regulating secretion from alveolar type II cells , 2001, The Journal of cell biology.

[21]  M W Berns,et al.  Parametric study of the forces on microspheres held by optical tweezers. , 1994, Applied optics.

[22]  W. Almers,et al.  Final steps in exocytosis observed in a cell with giant secretory granules. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[23]  Stephen R. Quake,et al.  The dynamics of partially extended single molecules of DNA , 1997, Nature.

[24]  M. Frick,et al.  Mechanisms of surfactant exocytosis in alveolar type II cells in vitro and in vivo. , 2001, News in physiological sciences : an international journal of physiology produced jointly by the International Union of Physiological Sciences and the American Physiological Society.

[25]  W. Betz,et al.  Simultaneous independent measurement of endocytosis and exocytosis , 1996, Nature.

[26]  T. Haller,et al.  Exocytosis in alveolar type II cells revealed by cell capacitance and fluorescence measurements. , 1999, The American journal of physiology.

[27]  S. Chu,et al.  Quantitative measurements of force and displacement using an optical trap. , 1996, Biophysical journal.

[28]  J. Zimmerberg,et al.  How can proteolipids be central players in membrane fusion? , 2001, Trends in cell biology.

[29]  B. Jena,et al.  Surface dynamics in living acinar cells imaged by atomic force microscopy: identification of plasma membrane structures involved in exocytosis. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[30]  M. Lindau,et al.  A novel Ca2+‐dependent step in exocytosis subsequent to vesicle fusion , 1995, FEBS letters.

[31]  J. Heuser,et al.  Arrest of membrane fusion events in mast cells by quick-freezing , 1980, The Journal of cell biology.

[32]  E. S. Horning Cell Physiology , 1954, Nature.

[33]  K. Pfaller,et al.  The conception of fusion pores as rate-limiting structures for surfactant secretion. , 2001, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.

[34]  M. Williams,et al.  An improved method for isolating type II cells in high yield and purity. , 2015, The American review of respiratory disease.

[35]  M. Frick,et al.  Secretion in alveolar type II cells at the interface of constitutive and regulated exocytosis. , 2001, American journal of respiratory cell and molecular biology.

[36]  V. Valero,et al.  High calcium concentrations shift the mode of exocytosis to the kiss-and-run mechanism , 1999, Nature Cell Biology.

[37]  G. Sonek,et al.  Evidence for localized cell heating induced by infrared optical tweezers. , 1995, Biophysical journal.

[38]  Michael P. Sheetz,et al.  Cell control by membrane–cytoskeleton adhesion , 2001, Nature Reviews Molecular Cell Biology.

[39]  S. Schürch,et al.  Formation and structure of surface films: captive bubble surfactometry. , 1998, Biochimica et biophysica acta.

[40]  R. J. Fisher,et al.  Control of fusion pore dynamics during exocytosis by Munc18. , 2001, Science.

[41]  W. Seeger,et al.  Role of actin depolymerization in the surfactant secretory response of alveolar epithelial type II cells. , 1999, American journal of respiratory and critical care medicine.

[42]  M. Frick,et al.  Threshold calcium levels for lamellar body exocytosis in type II pneumocytes. , 1999, American journal of physiology. Lung cellular and molecular physiology.