Brefeldin A: insights into the control of membrane traffic and organelle structure

THE definition of cellular organelles has evolved over the last hundred years largely driven by morphologic observations, but more recently has been supplemented and complemented by functional and biochemical studies (Palade, 1975) . Thus, organelles are now identified both by their morphology and by the set ofcomponents that comprise them . Determining how organelle identity is established and maintained and how newly synthesized protein and membrane are sorted to different organelles are the central issues of organellogenesis . Essential to the many cellular functions that take place within the central vacuolar system (which consists ofthe ER, Golgi apparatus, secretory vesicles, endosomes, and lysosomes) is membrane traffic which mediates the exchange of components between different organelles . There are two critical characteristics of membrane traffic . First, only certain sets oforganelles exchange membrane and the patterns of this exchange define what are called membrane pathways . Second, multiple pathways intersect at specific points within the central vacuolar system . For specific components to "choose" the correct pathway at such points of crossing, mechanisms exist to impose choices on specific molecules . This process is called sorting . The characteristicsofeachorganelle within the central vacuolar system are likely to be intimately tied to the properties ofmembrane traffic . An imbalance in the magnitude ofmembrane input into and egress from an organelle would have profound effects on the size ofthat compartment . In addition, failures in sorting or aberrations in targeting pathways would be expected to profoundly affect the identity of individual organelles . Recently, the relationship between the control of membrane traffic and the maintenance of organelle structure has been investigated with the use ofa remarkable drug, brefeldin A (BFA).' In this review we will summarize recent findings with BFA and propose some speculative models concerning the mechanism and regulation ofmembrane traffic within the central vacuolar system .

[1]  K. von Figura,et al.  Effects of brefeldin A on the endocytic route. Redistribution of mannose 6-phosphate/insulin-like growth factor II receptors to the cell surface. , 1991, The Journal of biological chemistry.

[2]  K. Howell,et al.  Vesicle budding: insights from cell-free assays. , 1991, Trends in cell biology.

[3]  H. Freeze,et al.  Uncoupling of chondroitin sulfate glycosaminoglycan synthesis by brefeldin A , 1991, The Journal of cell biology.

[4]  J. Lippincott-Schwartz,et al.  Binding of ARF and beta-COP to Golgi membranes: possible regulation by a trimeric G protein. , 1991, Science.

[5]  K. Sandvig,et al.  Ricin transport in brefeldin A-treated cells: correlation between Golgi structure and toxic effect , 1991, The Journal of cell biology.

[6]  I. Mellman,et al.  Selective inhibition of transcytosis by brefeldin A in MDCK cells , 1991, Cell.

[7]  W. Brown,et al.  Brefeldin A causes a microtubule-mediated fusion of the trans-Golgi network and early endosomes , 1991, Cell.

[8]  J. Lippincott-Schwartz,et al.  Brefeldin A's effects on endosomes, lysosomes, and the TGN suggest a general mechanism for regulating organelle structure and membrane traffic , 1991, Cell.

[9]  J. Tooze,et al.  Tubular early endosomal networks in AtT20 and other cells , 1991, The Journal of cell biology.

[10]  T. Hudson,et al.  Brefeldin-A enhancement of ricin A-chain immunotoxins and blockade of intact ricin, modeccin, and abrin. , 1991, The Journal of biological chemistry.

[11]  S. Wong,et al.  Inhibition by brefeldin A of protein secretion from the apical cell surface of Madin-Darby canine kidney cells. , 1991, The Journal of biological chemistry.

[12]  D. Sanan,et al.  Reconstitution of clathrin-coated pit budding from plasma membranes , 1991, The Journal of cell biology.

[13]  R. Kahn Fluoride is not an activator of the smaller (20-25 kDa) GTP-binding proteins. , 1991, The Journal of biological chemistry.

[14]  J. Lippincott-Schwartz,et al.  A recycling pathway between the endoplasmic reticulum and the Golgi apparatus for retention of unassembled MHC class I molecules , 1991, Nature.

[15]  Richard B. Vallee,et al.  Multiple forms of dynamin are encoded by shibire, a Drosophila gene involved in endocytosis , 1991, Nature.

[16]  G. Bloom,et al.  PtK1 cells contain a nondiffusible, dominant factor that makes the Golgi apparatus resistant to brefeldin A , 1991, The Journal of cell biology.

[17]  Alexander M. van der Bliek,et al.  Dynamin-like protein encoded by the Drosophila shibire gene associated with vesicular traffic , 1991, Nature.

[18]  P. Argos,et al.  β-COP, a 110 kd protein associated with non-clathrin-coated vesicles and the golgi complex, shows homology to β-adaptin , 1991, Cell.

[19]  J. Lippincott-Schwartz,et al.  Forskolin inhibits and reverses the effects of brefeldin A on Golgi morphology by a cAMP-independent mechanism , 1991, The Journal of cell biology.

[20]  J. Lippincott-Schwartz,et al.  Guanine nucleotides modulate the effects of brefeldin A in semipermeable cells: regulation of the association of a 110-kD peripheral membrane protein with the Golgi apparatus , 1991, The Journal of cell biology.

[21]  T. Yoshida,et al.  Disruption of the Golgi apparatus by brefeldin A inhibits the cytotoxicity of ricin, modeccin, and Pseudomonas toxin. , 1991, Experimental cell research.

[22]  J. Rothman,et al.  'Coatomer': a cytosolic protein complex containing subunits of non-clathrin-coated Golgi transport vesicles , 1991, Nature.

[23]  J. Rothman,et al.  A coat subunit of Golgi-derived non-clathrin-coated vesicles with homology to the clathrin-coated vesicle coat protein β-adaptin , 1991, Nature.

[24]  H. Geuze,et al.  Brefeldin A induces a microtubule‐dependent fusion of galactosyltransferase‐containing vesicles with the rough endoplasmic reticulum , 1991, Biology of the cell.

[25]  N. Takami,et al.  Intracellular accumulation and oligosaccharide processing of alkaline phosphatase under disassembly of the Golgi complex caused by brefeldin A. , 1990, European journal of biochemistry.

[26]  W. Balch Small GTP-binding proteins in vesicular transport. , 1990, Trends in biochemical sciences.

[27]  H. Hauri,et al.  Identification of an intermediate compartment involved in protein transport from endoplasmic reticulum to Golgi apparatus. , 1990, European journal of cell biology.

[28]  J. Lippincott-Schwartz,et al.  Dissociation of a 110-kD peripheral membrane protein from the Golgi apparatus is an early event in brefeldin A action , 1990, The Journal of cell biology.

[29]  D. Botstein,et al.  ADP ribosylation factor is an essential protein in Saccharomyces cerevisiae and is encoded by two genes , 1990, Molecular and cellular biology.

[30]  L. Ercolani,et al.  Membrane localization of the pertussis toxin-sensitive G-protein subunits αi-2 and αi-3 and expression of a metallothionein-αi-2 fusion gene in LLC-PK1 cells , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[31]  S. Mills,et al.  Use of brefeldin A to define sites of glycosphingolipid synthesis: GA2/GM2/GD2 synthase is trans to the brefeldin A block. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[32]  K. Howell,et al.  Identification, sequencing and expression of an integral membrane protein of the trans-Golgi network (TGN38). , 1990, The Biochemical journal.

[33]  H. Pelham,et al.  Recycling of proteins from the Golgi compartment to the ER in yeast , 1990, The Journal of cell biology.

[34]  M. Zerial,et al.  Localization of low molecular weight GTP binding proteins to exocytic and endocytic compartments , 1990, Cell.

[35]  Stephen J. Smith,et al.  Tubulovesicular processes emerge from trans-Golgi cisternae, extend along microtubules, and interlink adjacent trans-Golgi elements into a reticulum , 1990, Cell.

[36]  Y. Clermont,et al.  Three-dimensional electron microscopy: structure of the Golgi apparatus. , 1990, European journal of cell biology.

[37]  J. Lippincott-Schwartz,et al.  Microtubule-dependent retrograde transport of proteins into the ER in the presence of brefeldin a suggests an ER recycling pathway , 1990, Cell.

[38]  S. Yamashina,et al.  Morphological effects of brefeldin A on the intracellular transport of secretory materials in parotid acinar cells. , 1990, Cell structure and function.

[39]  D. Botstein,et al.  ADP-ribosylation factor is functionally and physically associated with the Golgi complex. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[40]  M. Robinson,et al.  Clathrin, adaptors, and sorting. , 1990, Annual review of cell biology.

[41]  J. Lippincott-Schwartz,et al.  The T cell antigen receptor: insights into organelle biology. , 1990, Annual review of cell biology.

[42]  Y. Ikehara,et al.  Dynamic distribution of the Golgi marker thiamine pyrophosphatase is modulated by brefeldin A in rat hepatoma cells. , 1989, Cell structure and function.

[43]  G. Palade,et al.  Targeting and processing of glycophorins in murine erythroleukemia cells: use of brefeldin A as a perturbant of intracellular traffic. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[44]  J. Rothman,et al.  Purification of a novel class of coated vesicles mediating biosynthetic protein transport through the Golgi stack , 1989, Cell.

[45]  R. Doms,et al.  Brefeldin A redistributes resident and itinerant Golgi proteins to the endoplasmic reticulum , 1989, The Journal of cell biology.

[46]  J. Bonifacino,et al.  Brefeldin A implicates egress from endoplasmic reticulum in class I restricted antigen presentation , 1989, Nature.

[47]  J. Lippincott-Schwartz,et al.  Rapid redistribution of Golgi proteins into the ER in cells treated with brefeldin A: Evidence for membrane cycling from Golgi to ER , 1989, Cell.

[48]  J. Heuser Changes in lysosome shape and distribution correlated with changes in cytoplasmic pH , 1989, The Journal of cell biology.

[49]  J. Rothman,et al.  Dissection of a single round of vesicular transport: Sequential intermediates for intercisternal movement in the Golgi stack , 1989, Cell.

[50]  K. Howell,et al.  Membrane traffic in endocytosis: insights from cell-free assays. , 1989, Annual review of cell biology.

[51]  Y. Ikehara,et al.  Brefeldin A causes disassembly of the Golgi complex and accumulation of secretory proteins in the endoplasmic reticulum. , 1988, The Journal of biological chemistry.

[52]  H. Hauri,et al.  Identification, by a monoclonal antibody, of a 53-kD protein associated with a tubulo-vesicular compartment at the cis-side of the Golgi apparatus , 1988, The Journal of cell biology.

[53]  S. Dabora,et al.  The microtubule-dependent formation of a tubulovesicular network with characteristics of the ER from cultured cell extracts , 1988, Cell.

[54]  H. Bourne Do GTPases direct membrane traffic in secretion? , 1988, Cell.

[55]  H. Pelham Evidence that luminal ER proteins are sorted from secreted proteins in a post‐ER compartment. , 1988, The EMBO journal.

[56]  D. S. Keller,et al.  Semi-intact cells permeable to macromolecules: Use in reconstitution of protein transport from the endoplasmic reticulum to the Golgi complex , 1987, Cell.

[57]  J. Lippincott-Schwartz,et al.  Cycling of the integral membrane glycoprotein, LEP100, between plasma membrane and lysosomes: Kinetic and morphological analysis , 1987, Cell.

[58]  G. Warren Signals and salvage sequences , 1987, Nature.

[59]  Y. Misumi,et al.  Brefeldin A arrests the intracellular transport of a precursor of complement C3 before its conversion site in rat hepatocytes , 1987, FEBS letters.

[60]  A. Gilman,et al.  G proteins: transducers of receptor-generated signals. , 1987, Annual review of biochemistry.

[61]  T. Kreis,et al.  A microtubule-binding protein associated with membranes of the Golgi apparatus , 1986, The Journal of cell biology.

[62]  K. Simons,et al.  The trans Golgi network: sorting at the exit site of the Golgi complex. , 1986, Science.

[63]  K. Fujiwara,et al.  Microtubules and the endoplasmic reticulum are highly interdependent structures , 1986, The Journal of cell biology.

[64]  Y. Misumi,et al.  Novel blockade by brefeldin A of intracellular transport of secretory proteins in cultured rat hepatocytes. , 1986, The Journal of biological chemistry.

[65]  A. Tartakoff Temperature and energy dependence of secretory protein transport in the exocrine pancreas. , 1986, The EMBO journal.

[66]  A. Helenius,et al.  Three-dimensional structure of endosomes in BHK-21 cells. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[67]  A. Takatsuki,et al.  Brefeldin a, a specific inhibitor of intracellular translocation of vesicular stomatitis virus G protein: Intracellular accumulation of high-mannose type G protein and inhibition of its cell surface expression , 1985 .

[68]  R. Schekman Protein localization and membrane traffic in yeast. , 1985, Annual review of cell biology.

[69]  J. Rothman,et al.  Sequential intermediates in the pathway of intercompartmental transport in a cell-free system , 1984, Cell.

[70]  J. Slot,et al.  Intracellular receptor sorting during endocytosis: Comparative immunoelectron microscopy of multiple receptors in rat liver , 1984, Cell.

[71]  A. Gilman,et al.  The subunits of the stimulatory regulatory component of adenylate cyclase. Resolution of the activated 45,000-dalton (alpha) subunit. , 1983, The Journal of biological chemistry.

[72]  H. Lodish,et al.  Intracellular site of asialoglycoprotein receptor-ligand uncoupling: Double-label immunoelectron microscopy during receptor-mediated endocytosis , 1983, Cell.

[73]  K. Arima,et al.  Antiviral activity of brefeldin A and verrucarin A. , 1968, The Journal of antibiotics.

[74]  W. Loeffler,et al.  Über die Isolierung neuer Stoffwechselprodukte aus Penicillium brefeldianum DODGE , 1963 .