The microfilament cytoskeleton plays a vital role in salt and osmotic stress tolerance in Arabidopsis.

Although recent studies have suggested that the microfilament (MF) cytoskeleton of plant cells participates in the response to salt stress, it remains unclear as to whether the MF cytoskeleton actually plays an active role in a plant's ability to withstand salt stress. In the present study, we report for the first time the role of MFs in salt tolerance of Arabidopsis thaliana. Our experiments revealed that Arabidopsis seedlings treated with 150 mm NaCl maintained MF assembly and bundle formation, whereas treatment with 250 mm NaCl initially induced MF assembly but subsequently caused MF disassembly. A corresponding change in the fluorescence intensity of MFs was also observed; that is, a sustained rise in fluorescence intensity in seedlings exposed to 150 mm NaCl and an initial rise and subsequent fall in seedlings exposed to 250 mm NaCl. These results suggest that MF assembly and bundles are induced early after salt stress treatment, while MF polymerization disappears after high salt stress. Facilitation of MF assembly with phalloidin rescued wild-type seedlings from death, whereas blocking MFs assembly with latrunculin A and cytochalasin D resulted in few survivors under salt stress. Pre-treatment of seedlings with phalloidin also clearly increased plant ability to withstand salt stress. MF assembly increased survival of Arabidopsis salt-sensitive sos2 mutants under salt stress and rescued defective sos2 mutants. Polymerization of MFs and its role in promoting survival was also found in plants exposed to osmotic stress. These findings suggest that the MF cytoskeleton participates and plays a vital role in responses to salt and osmotic stress in Arabidopsis.

[1]  M. Yuan,et al.  Salt tolerance requires cortical microtubule reorganization in Arabidopsis. , 2007, Plant & cell physiology.

[2]  Lifeng Jin,et al.  SB401, a pollen-specific protein from Solanum berthaultii, binds to and bundles microtubules and F-actin. , 2007, The Plant journal : for cell and molecular biology.

[3]  Lifeng Jin,et al.  Arabidopsis MICROTUBULE-ASSOCIATED PROTEIN18 Functions in Directional Cell Growth by Destabilizing Cortical Microtubules , 2007, The Plant Cell Online.

[4]  A. Rus,et al.  Salt stress affects cortical microtubule organization and helical growth in Arabidopsis. , 2006, Plant & cell physiology.

[5]  R. Ranjeva,et al.  Calcium in plant defence-signalling pathways. , 2006, The New phytologist.

[6]  Patrick Achard,et al.  Integration of Plant Responses to Environmentally Activated Phytohormonal Signals , 2006, Science.

[7]  Laurie G. Smith,et al.  Spatial control of cell expansion by the plant cytoskeleton. , 2005, Annual review of cell and developmental biology.

[8]  F. Baluška,et al.  GFP-FABD2 fusion construct allows in vivo visualization of the dynamic actin cytoskeleton in all cells of Arabidopsis seedlings. , 2005, European journal of cell biology.

[9]  Ying Fu,et al.  Arabidopsis Interdigitating Cell Growth Requires Two Antagonistic Pathways with Opposing Action on Cell Morphogenesis , 2005, Cell.

[10]  Viswanathan Chinnusamy,et al.  Understanding and Improving Salt Tolerance in Plants , 2005 .

[11]  M. Lagarde,et al.  Phospholipase D is involved in myogenic differentiation through remodeling of actin cytoskeleton. , 2005, Molecular biology of the cell.

[12]  T. Shimmen,et al.  Ca2+-induced fragmentation of actin filaments in pollen tubes , 1987, Protoplasma.

[13]  Zhenbiao Yang,et al.  New Views on the Plant Cytoskeleton , 2004, Plant Physiology.

[14]  D. McCurdy,et al.  A Green Fluorescent Protein Fusion to Actin-Binding Domain 2 of Arabidopsis Fimbrin Highlights New Features of a Dynamic Actin Cytoskeleton in Live Plant Cells1[w] , 2004, Plant Physiology.

[15]  C. Staiger,et al.  The role of the actin cytoskeleton in plant cell signaling. , 2004, The New phytologist.

[16]  J. Petrášek,et al.  Sites of actin filament initiation and reorganization in cold‐treated tobacco cells , 2004 .

[17]  H. Matsubara,et al.  SPIRAL1 Encodes a Plant-Specific Microtubule-Localized Protein Required for Directional Control of Rapidly Expanding Arabidopsis Cells , 2004, The Plant Cell Online.

[18]  Jian-Kang Zhu,et al.  Regulation of Ion Homeostasis under Salt Stress , 2015 .

[19]  R. Vera-Estrella,et al.  Na+/H+ Exchange Activity in the Plasma Membrane of Arabidopsis1 , 2003, Plant Physiology.

[20]  A. Cheung,et al.  Actin-Depolymerizing Factor Mediates Rac/Rop GTPase–Regulated Pollen Tube Growth Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.007153. , 2003, The Plant Cell Online.

[21]  Xuemin Wang Phospholipase D in hormonal and stress signaling. , 2002, Current opinion in plant biology.

[22]  Q. Qiu,et al.  Regulation of SOS1, a plasma membrane Na+/H+ exchanger in Arabidopsis thaliana, by SOS2 and SOS3 , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[23]  Jian-Kang Zhu,et al.  Cell Signaling during Cold, Drought, and Salt Stress Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.000596. , 2002, The Plant Cell Online.

[24]  Jian-Kang Zhu,et al.  The Putative Plasma Membrane Na+/H+ Antiporter SOS1 Controls Long-Distance Na+ Transport in Plants Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.010371. , 2002, The Plant Cell Online.

[25]  S. Ryu,et al.  Actin Directly Interacts with Phospholipase D, Inhibiting Its Activity* , 2001, The Journal of Biological Chemistry.

[26]  J. Mathur,et al.  Inactivation of AtRac1 by abscisic acid is essential for stomatal closure. , 2001, Genes & development.

[27]  Y. Lee,et al.  Abscisic acid-induced actin reorganization in guard cells of dayflower is mediated by cytosolic calcium levels and by protein kinase and protein phosphatase activities. , 2001, Plant physiology.

[28]  J. Zhu,et al.  Plant salt tolerance. , 2001, Trends in plant science.

[29]  D. Barber,et al.  Direct binding of the Na--H exchanger NHE1 to ERM proteins regulates the cortical cytoskeleton and cell shape independently of H(+) translocation. , 2000, Molecular cell.

[30]  O. Rotstein,et al.  Hypertonic inhibition of exocytosis in neutrophils: central role for osmotic actin skeleton remodeling. , 2000, American journal of physiology. Cell physiology.

[31]  R. Dhindsa,et al.  Early steps in cold sensing by plant cells: the role of actin cytoskeleton and membrane fluidity. , 2000, The Plant journal : for cell and molecular biology.

[32]  J. Mills,et al.  Role of the F-actin cytoskeleton in the RVD and RVI processes in Ehrlich ascites tumor cells. , 1999, Experimental cell research.

[33]  R. Ranjeva,et al.  Organization of cytoskeleton controls the changes in cytosolic calcium of cold-shocked Nicotiana plumbaginifolia protoplasts. , 1997, Cell calcium.

[34]  K. Hallows,et al.  Changes in cytoskeletal actin content, F‐actin distribution, and surface morphology during HL‐60 cell volume regulation , 1996, Journal of cellular physiology.

[35]  T. Flowers,et al.  Breeding for salinity resistance in crop plants: Where next? , 1995 .

[36]  K. Hallows,et al.  Acute cell volume changes in anisotonic media affect F-actin content of HL-60 cells. , 1991, The American journal of physiology.

[37]  P. Hasegawa,et al.  Enhanced Net K Uptake Capacity of NaCl-Adapted Cells. , 1991, Plant physiology.

[38]  P. Hasegawa,et al.  Cellular Mechanisms of Salinity Tolerance , 1986, HortScience.