Stabilization of Exocytosis by Dynamic F-actin Coating of Zymogen Granules in Pancreatic Acini*

Reorganization of F-actin in the apical region of mouse pancreatic acinar cells during Ca2+-dependent exocytosis of zymogen granules was investigated by two-photon excitation microscopy with intact acini. Granules were rapidly coated with F-actin in response to either agonist stimulation or photolysis of a caged-Ca2+ compound. Such F-actin coating occurred exclusively at the surface of granules undergoing exocytosis and was prevented either by latrunculin-A, which inhibits actin polymerization, or by Clostridium botulinum exoenzyme C3, which inhibits the small GTPase Rho. Latrunculin-A or exoenzyme C3 also triggered the formation of vacuoles in acinar cells, a characteristic of acute pancreatitis. Stimulation of acini with high concentrations of cholecystokinin, which cause acute pancreatitis in mice, also impaired the F-actin coating of granules and induced vacuole formation. Latrunculin-A reduced the latency to exocytosis but did not affect the total number of exocytic events, suggesting that F-actin slows and further stabilizes exocytosis by facilitating F-actin coating. Rho-dependent F-actin coating of granule membranes thus stabilizes exocytic structures and is necessary for physiological progression of sequetial compound exocytosis in the exocrine pancreas and for prevention of acute pancreatitis.

[1]  P. Janmey,et al.  Phosphoinositide regulation of the actin cytoskeleton. , 2003, Annual review of physiology.

[2]  Haruo Kasai,et al.  Cytosolic Ca2+ gradients triggering unidirectional fluid secretion from exocrine pancreas , 1990, Nature.

[3]  H. Kasai,et al.  Sequential exocytosis of insulin granules is associated with redistribution of SNAP25 , 2004, The Journal of cell biology.

[4]  J. Valentijn,et al.  Role of actin in regulated exocytosis and compensatory membrane retrieval: insights from an old acquaintance. , 1999, Biochemical and biophysical research communications.

[5]  G. Palade,et al.  Intracellular aspects of the process of protein synthesis. , 1975, Science.

[6]  S. Narumiya,et al.  Preparation of native and recombinant Clostridium botulinum C3 ADP-ribosyltransferase and identification of Rho proteins by ADP-ribosylation. , 1995, Methods in enzymology.

[7]  J. Mayerle,et al.  Presence of Cathepsin B in the Human Pancreatic Secretory Pathway and Its Role in Trypsinogen Activation during Hereditary Pancreatitis* , 2002, The Journal of Biological Chemistry.

[8]  S. Muallem,et al.  Actin filament disassembly is a sufficient final trigger for exocytosis in nonexcitable cells , 1995, The Journal of cell biology.

[9]  C Vaillant,et al.  Calcium-dependent enzyme activation and vacuole formation in the apical granular region of pancreatic acinar cells. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[10]  E. Bradley Acute pancreatitis : diagnosis and therapy , 1994 .

[11]  G. Adler,et al.  Exocytosis occurs at the lateral plasma membrane of the pancreatic acinar cell during supramaximal secretagogue stimulation. , 1987, Gastroenterology.

[12]  Y. Miyashita,et al.  Micromolar and submicromolar Ca2+ spikes regulating distinct cellular functions in pancreatic acinar cells , 1997, The EMBO journal.

[13]  R. Sutton,et al.  Is an elevated concentration of acinar cytosolic free ionised calcium the trigger for acute pancreatitis? , 1995, The Lancet.

[14]  M. Steer,et al.  Early events in acute pancreatitis. , 1999, Bailliere's best practice & research. Clinical gastroenterology.

[15]  A. Bretscher,et al.  Villin is a major protein of the microvillus cystoskeleton which binds both G and F actin in a calcium-dependent manner , 1980, Cell.

[16]  S. Pandol,et al.  Effects of caerulein on the apical cytoskeleton of the pancreatic acinar cell. , 1990, The Journal of clinical investigation.

[17]  A. Ichikawa FINE STRUCTURAL CHANGES IN RESPONSE TO HORMONAL STIMULATION OF THE PERFUSED CANINE PANCREAS , 1965, The Journal of cell biology.

[18]  A. Hall,et al.  Rho GTPases in cell biology , 2002, Nature.

[19]  J. Valentijn,et al.  Actin coating of secretory granules during regulated exocytosis correlates with the release of rab3D. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[20]  Haruo Kasai,et al.  Fusion Pore Dynamics and Insulin Granule Exocytosis in the Pancreatic Islet , 2002, Science.

[21]  A. Hall,et al.  Rho GTPases and the actin cytoskeleton. , 1998, Science.

[22]  S. Perry,et al.  The effect of denervation on the distribution of the polymorphic forms of troponin components in fast and slow muscles of the adult rat , 2004, Cell and Tissue Research.

[23]  U. Walter,et al.  Actin-based motility: stop and go with Ena/VASP proteins. , 2001, Trends in biochemical sciences.

[24]  S. Muallem,et al.  The Mammalian Sec6/8 Complex Interacts with Ca2+ Signaling Complexes and Regulates Their Activity , 2000, The Journal of cell biology.

[25]  S. Brenner,et al.  Inhibition of actin polymerization by latrunculin A , 1987, FEBS letters.

[26]  L. Orci,et al.  Pancreatic Beta-Cell Web: Its Possible Role in Insulin Secretion , 1972, Science.

[27]  K. Miyake,et al.  An actin barrier to resealing. , 2001, Journal of cell science.

[28]  S. Ross,et al.  A Role for the p38 Mitogen-activated Protein Kinase/Hsp 27 Pathway in Cholecystokinin-induced Changes in the Actin Cytoskeleton in Rat Pancreatic Acini* , 1998, The Journal of Biological Chemistry.

[29]  J. Cooper,et al.  Effects of cytochalasin and phalloidin on actin , 1987, The Journal of cell biology.

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

[31]  M. Lampel,et al.  Acute interstitial pancreatitis in the rat induced by excessive doses of a pancreatic secretagogue , 1977, Virchows Archiv A.

[32]  S. Halpain,et al.  Actin and the agile spine: how and why do dendritic spines dance? , 2000, Trends in Neurosciences.

[33]  N. Sahara,et al.  Lateral diffusion of luminal membrane components during secretion in parotid acinar cells of the rat , 1990, Cell and Tissue Research.

[34]  H. Mannherz,et al.  Distribution of actin and the actin-associated proteins myosin, tropomyosin, alpha-actinin, vinculin, and villin in rat and bovine exocrine glands. , 1983, European journal of cell biology.

[35]  E. Fuchs,et al.  Crossroads on Cytoskeletal Highways , 1999, Cell.

[36]  A. Dąbrowski,et al.  Cholecystokinin activates a variety of intracellular signal transduction mechanisms in rodent pancreatic acinar cells. , 2002, Pharmacology & toxicology.

[37]  P. De Camilli,et al.  Dynamic changes of the luminal plasmalemma in stimulated parotid acinar cells. A freeze-fracture study , 1976, The Journal of cell biology.

[38]  P C Sternweis,et al.  Direct stimulation of the guanine nucleotide exchange activity of p115 RhoGEF by Galpha13. , 1998, Science.

[39]  J. Taunton,et al.  Cdc42-dependent actin polymerization during compensatory endocytosis in Xenopus eggs , 2003, Nature Cell Biology.

[40]  M. McNiven,et al.  Agonist‐induced changes in cell shape during regulated secretion in rat pancreatic acini , 2000, Journal of cellular physiology.

[41]  W. Denk,et al.  Two-photon laser scanning fluorescence microscopy. , 1990, Science.

[42]  P. Janmey,et al.  Functional comparison of villin and gelsolin. Effects of Ca2+, KCl, and polyphosphoinositides. , 1988, The Journal of biological chemistry.