Adhesion strategies of Dictyostelium discoideum – a force spectroscopy study
Source abstract
Abstract
Biological adhesion is essential for all motile cells and generally limits locomotion to suitably functionalized substrates displaying a compatible surface chemistry. However, organisms that face vastly varying environmental challenges require a different strategy. The model organism Dictyostelium discoideum (D.d.), a slime mould dwelling in the soil, faces the challenge of overcoming variable chemistry by employing the fundamental forces of colloid science. To understand the origin of D.d. adhesion, we realized and modified a variety of conditions for the amoeba comprising the absence and presence of the specific adhesion protein Substrate Adhesion A (sadA), glycolytic degradation, ionic strength, surface hydrophobicity and strength of van der Waals interactions by generating tailored model substrates. By employing AFM-based single cell force spectroscopy we could show that experimental force curves upon retraction exhibit two regimes. The first part up to the critical adhesion force can be described in terms of a continuum model, while the second regime of the curve beyond the critical adhesion force is governed by stochastic unbinding of individual binding partners and bond clusters. We found that D.d. relies on adhesive interactions based on EDL-DLVO (Electrical Double Layer-Derjaguin-Landau-Verwey-Overbeek) forces and contributions from the glycocalix and specialized adhesion molecules like sadA. This versatile mechanism allows the cells to adhere to a large variety of natural surfaces under various conditions.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Force Microscopy Techniques and Applications · Cellular Mechanics and Interactions · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Max Planck Institute for Dynamics and Self-Organization
37077 Göttingen
Germany
University of Goettingen
Institute for Non-linear Dynamics
Institute for Physical Chemistry
Funding
Max-Planck-Gesellschaft · Volkswagen Foundation · Deutsche Forschungsgemeinschaft
References (84)
Show source-provided references
1. R. H. Kessin , Dictyostelium: evolution, cell biology, and the development of multicellularity , Cambridge University Press , 2001 , vol. 3810.1017/CBO9780511525315 ↗
2. Devreotes · Annu. Rev. Cell Dev. Biol. · 2017 · 33 · 10310.1146/annurev-cellbio-100616-060739 ↗
3. Stuelten · Nat. Rev. Cancer · 2018 · 29610.1038/nrc.2018.15 ↗
4. Bäumchen · Phys. J. · 2015 · 14 · 37
5. Kreis · Nat. Phys. · 2018 · 14 · 4510.1038/nphys4258 ↗
6. Dufrêne · Trends Microbiol. · 2015 · 23 · 37610.1016/j.tim.2015.01.011 ↗
7. T. Pollard , W.Earnshaw and J.Lippincott-Schwartz , Cell biology , Springer Spektrum , Heidelberg , 2007
8. Sebe-Pedros · Proc. Natl. Acad. Sci. U. S. A. · 2010 · 107 · 1014210.1073/pnas.1002257107 ↗
9. Varnum · Dev. Biol. · 1986 · 113 · 21810.1016/0012-1606(86)90124-7 ↗
10. Gerisch · Cell Motil. Cytoskeleton · 1989 · 14 · 7510.1002/cm.970140115 ↗
11. Weber · J. Cell Sci. · 1995 · 108 · 151910.1242/jcs.108.4.1519 ↗
12. J. Israelachvili , Intermolecular and surface forces , Academic Press , 1992 , p. 437
13. V. Parsegian , Van der Waals Forces , Cambridge University Press , 2006 , p. 398
14. Leckband · Q. Rev. Biophys. · 2001 · 34 · 10510.1017/S0033583501003687 ↗
15. Bell · Science · 1978 · 61810.1126/science.347575 ↗
16. Sackmann · Soft Matter · 2014 · 10 · 164410.1039/c3sm51910d ↗
17. D. Boal , Mechanics of the cell , Cambridge University Press , Cambridge , 201210.1017/CBO9781139022217 ↗
18. Kowal · Eukaryotic Cell · 2011 · 10 · 66210.1128/EC.00221-10 ↗
19. Fey · J. Cell Biol. · 2002 · 159 · 110910.1083/jcb.200206067 ↗
20. Vinet · Mol. Biol. Cell · 2014 · 25 · 68810.1091/mbc.e13-04-0219 ↗
21. Zaidel-Bar · Nat. Cell Biol. · 2007 · 9 · 85810.1038/ncb0807-858 ↗
22. Harwood · Curr. Opin. Cell Biol. · 2004 · 16 · 47010.1016/j.ceb.2004.07.011 ↗
23. Swaminathan · Sci. Rep. · 2015 · 5 · 1443710.1038/srep14437 ↗
24. Bukahrova · J. Cell Sci. · 2005 · 118 · 429510.1242/jcs.02557 ↗
25. Tsujioka · Proc. Natl. Acad. Sci. U. S. A. · 2012 · 109 · 1299210.1073/pnas.1208296109 ↗
26. Niewohner · J. Cell Biol. · 1997 · 138 · 34910.1083/jcb.138.2.349 ↗
27. Cornillon · Eukaryotic Cell · 2008 · 7 · 160010.1128/EC.00155-08 ↗
28. Cornillon · EMBO Rep. · 2006 · 7 · 61710.1038/sj.embor.7400701 ↗
29. Cornillon · J. Biol. Chem. · 2000 · 275 · 3428710.1074/jbc.M006725200 ↗
30. Froquet · Mol. Biol. Cell · 2012 · 23 · 67910.1091/mbc.e11-04-0338 ↗
31. Perrin · J. Cell Sci. · 2015 · 128 · 226910.1242/jcs.164848 ↗
32. Benoit · Nat. Cell Biol. · 2000 · 2 · 31310.1038/35014000 ↗
33. Miao · Nat. Cell Biol. · 2017 · 19 · 32910.1038/ncb3495 ↗
34. Pietuch · Biochim. Biophys. Acta, Mol. Cell Res. · 2013 · 1833 · 71210.1016/j.bbamcr.2012.11.006 ↗
35. Lusche · Cell Motil. Cytoskeleton · 2009 · 66 · 56710.1002/cm.20367 ↗
36. Loskill · Langmuir · 2012 · 28 · 724210.1021/la3004323 ↗
37. Loomis · PLoS One · 2012 · 7 · e4203310.1371/journal.pone.0042033 ↗
38. Sun · Proc. Natl. Acad. Sci. U. S. A. · 2015 · 112 · 1255710.1073/pnas.1502970112 ↗
39. Driscoll · ACS Nano · 2014 · 8 · 354610.1021/nn406637c ↗
40. Lessel · Surf. Interface Anal. · 2015 · 47 · 55710.1002/sia.5729 ↗
41. Hutter · Rev. Sci. Instrum. · 1993 · 64 · 186810.1063/1.1143970 ↗
42. Cannara · Rev. Sci. Instrum. · 2006 · 77 · 05370110.1063/1.2198768 ↗
43. Tarantola · PLoS One · 2014 · 9 · e10657410.1371/journal.pone.0106574 ↗
44. Schindelin · Nat. Methods · 2012 · 9 · 67610.1038/nmeth.2019 ↗
45. S. Vogel , Comparative biomechanics: life's physical world , Princeton University Press , 2013
46. Brochard-Wyart · C. R. Phys. · 2003 · 4 · 28110.1016/S1631-0705(03)00048-3 ↗
47. Schäfer · Soft Matter · 2015 · 11 · 448710.1039/C5SM00191A ↗
48. E. A. Evans and R.Skalak , Mechanics and Thermodynamics of Biomembranes , CRC Press , 1980 , p. 254
49. Lin · Int. J. Solids Struct. · 2007 · 44 · 192710.1016/j.ijsolstr.2006.09.006 ↗
50. Wang · J. Mater. Sci. · 1995 · 30 · 317110.1007/BF01209233 ↗
51. Daily · Biophys. J. · 1984 · 45 · 67110.1016/S0006-3495(84)84209-5 ↗
52. Lipowsky · Mol. Cryst. Liq. Cryst. · 1991 · 202 · 1710.1080/00268949108035656 ↗
53. Bormashenko · Colloids Surf., A · 2009 · 345 · 16310.1016/j.colsurfa.2009.04.054 ↗
54. Lubarda · Soft Matter · 2012 · 8 · 1028810.1039/c2sm25740h ↗
55. Barthel · J. Phys. D: Appl. Phys. · 2008 · 41 · 16300110.1088/0022-3727/41/16/163001 ↗
56. Stewart · Methods · 2013 · 60 · 18610.1016/j.ymeth.2013.02.015 ↗
57. Sariisik · Biophys. J. · 2015 · 109 · 133010.1016/j.bpj.2015.07.048 ↗
58. Sackmann · ChemPhysChem · 2002 · 3 · 26210.1002/1439-7641(20020315)3:3<262::AID-CPHC262>3.0.CO;2-U ↗
59. Sen · Biophys. J. · 2005 · 89 · 320310.1529/biophysj.105.063826 ↗
60. Schwarz · Rev. Mod. Phys. · 2013 · 85 · 132710.1103/RevModPhys.85.1327 ↗
61. Diz-Muñoz · Nat. Phys. · 2018 · 14 · 64810.1038/s41567-018-0187-8 ↗
62. Krieg · Angew. Chem., Int. Ed. · 2008 · 47 · 977510.1002/anie.200803552 ↗
63. Colbert · Biophys. J. · 2010 · 99 · 355510.1016/j.bpj.2010.10.008 ↗
64. Simson · Biophys. J. · 1998 · 74 · 51410.1016/S0006-3495(98)77808-7 ↗
65. Kuo · Nat. Phys. · 2018 · 14 · 65810.1038/s41567-018-0186-9 ↗
66. Driscoll · ACS Nano · 2014 · 8 · 354610.1021/nn406637c ↗
67. Nagel · PLoS One · 2014 · 9 · e11338210.1371/journal.pone.0113382 ↗
68. Jasnin · Structure · 2016 · 24 · 103110.1016/j.str.2016.05.004 ↗
69. Priebe · Biophys. J. · 2014 · 107 · 266210.1016/j.bpj.2014.10.027 ↗
70. Helenius · Biophys. J. · 2018 · 115 · 15010.1016/j.bpj.2018.05.025 ↗
71. Knoch · Phys. Biol. · 2014 · 11 · 04600210.1088/1478-3975/11/4/046002 ↗
72. Hellio · J. Cell Sci. · 1985 · 79 · 32710.1242/jcs.79.1.327 ↗
73. Socol · Bioelectrochemistry · 2010 · 79 · 19810.1016/j.bioelechem.2010.04.003 ↗
74. Maeda · Dev., Growth Differ. · 1980 · 22 · 67910.1111/j.1440-169X.1980.00679.x ↗
75. Rao · Cell · 1995 · 82 · 13110.1016/0092-8674(95)90059-4 ↗
76. Ramezanian · Biointerphases · 2018 · 13 · 04100510.1116/1.5027735 ↗
77. Leonhardt · Phys. Rev. E · 2016 · 93 · 01241410.1103/PhysRevE.93.012414 ↗
78. Thewes · Beilstein J. Nanotechnol. · 2014 · 5 · 150110.3762/bjnano.5.163 ↗
79. Wang · J. R. Soc., Interface · 2014 · 11 · 2014068410.1098/rsif.2014.0684 ↗
80. Lampert · Proc. Natl. Acad. Sci. U. S. A. · 2017 · 114 · E772710.1073/pnas.1616600114 ↗
81. McCann · PLoS One · 2014 · 9 · e8798110.1371/journal.pone.0087981 ↗
82. Driscoll · PLoS Comput. Biol. · 2012 · 8 · e100239210.1371/journal.pcbi.1002392 ↗
83. Bae · Proc. Natl. Acad. Sci. U. S. A. · 2010 · 107 · E16510.1073/pnas.1011900107 ↗
84. Barry · Proc. Natl. Acad. Sci. U. S. A. · 2010 · 107 · 1137610.1073/pnas.1006327107 ↗