Insight into the role of cholesterol in modulation of morphology and mechanical properties of CHO-K1 cells: An in situ AFM study
Lei Zhang, Lisha Zhao, Ping-Kai Ouyang, Pu Chen
Insight into the role of cholesterol in modulation of morphology and mechanical properties of CHO-K1 cells: An in situ AFM study
Cholesterol plays a significant role in the organization of lipids and modulation of membrane dynamics in mammalian cells. However, the effect of cholesterol depletion on the eukaryotic cell membranes seems controversial. In this study, the effects of cholesterol on the topography and mechanical behaviors of CHO-K1 cells with manipulated membrane cholesterol contents were investigated by atomic force microscopy (AFM) technique. Here, we found that the depletion of cholesterol in cell membranes could increase the membrane stiffness, reduce the cell height as well as promote cell retraction and detachment from the surface, whereas the cholesterol restoration could reverse the effect of cholesterol depletion on the membrane stiffness. Increased methyl-β-cyclodextrin levels and incubation time could significantly increase Young’s modulus and degree of stiffing on cell membrane and cytoskeleton. This research demonstratede importance of cholesterol in regulating the dynamics of cytoskeleton-mediated processes. AFM technique offers excellent advantages in the dynamic monitoring of the change in membranes mechanical properties and behaviors during the imaging process. This promising technology can be utilized in studying the membrane properties and elucidating the underlying mechanism of distinct cells in the near-native environment.
cholesterol / methyl-β-cyclodextrin / atomic force microscopy / Young’s modulus / CHO-K1 cell
[1] |
de Oliveira Andrade L. Understanding the role of cholesterol in cellular biomechanics and regulation of vesicular trafficking: The power of imaging. Biomedical Spectroscopy and Imaging, 2016, 5(s1): S101–S117
CrossRef
Google scholar
|
[2] |
Evangelisti E, Cecchi C, Cascella R, Sgromo C, Becatti M, Dobson C M, Chiti F, Stefani M. Membrane lipid composition and its physicochemical properties define cell vulnerability to aberrant protein oligomers. Journal of Cell Science, 2012, 125(10): 2416–2427
CrossRef
Google scholar
|
[3] |
Redondo-Morata L, Giannotti M I, Sanz F. Influence of cholesterol on the phase transition of lipid bilayers: A temperature-controlled force spectroscopy study. Langmuir, 2012, 28(35): 12851–12860
CrossRef
Google scholar
|
[4] |
Zhao L, Temelli F. Preparation of liposomes using supercritical carbon dioxide via depressurization of the supercritical phase. Journal of Food Engineering, 2015, 158: 104–112
CrossRef
Google scholar
|
[5] |
Magarkar A, Dhawan V, Kallinteri P, Viitala T, Elmowafy M, Rog T, Bunker A. Cholesterol level affects surface charge of lipid membranes in saline solution. Scientific Reports, 2014, 4: 2045–2322
|
[6] |
Zhao L, Temelli F, Curtis J M, Chen L. Encapsulation of lutein in liposomes using supercritical carbon dioxide. Food Research International, 2017, 100: 168–179
CrossRef
Google scholar
|
[7] |
de Meyer F, Smit B. Effect of cholesterol on the structure of a phospholipid bilayer. Proceedings of the National Academy of Sciences of the United States of America, 2009, 106(10): 3654–3658
CrossRef
Google scholar
|
[8] |
Sułkowski W, Pentak D, Nowak K, Sułkowska A. The influence of temperature, cholesterol content and pH on liposome stability. Journal of Molecular Structure, 2005, 744: 737–747
CrossRef
Google scholar
|
[9] |
Zhao L, Temelli F, Curtis J M, Chen L. Preparation of liposomes using supercritical carbon dioxide technology: Effects of phospholipids and sterols. Food Research International, 2015, 77: 63–72
CrossRef
Google scholar
|
[10] |
Zhao L, Temelli F. Preparation of liposomes using a modified supercritical process via depressurization of liquid phase. Journal of Supercritical Fluids, 2015, 100: 110–120
CrossRef
Google scholar
|
[11] |
Khatibzadeh N, Spector A A, Brownell W E, Anvari B. Effects of plasma membrane cholesterol level and cytoskeleton F-actin on cell protrusion mechanics. PLoS One, 2013, 8(2): e57147
CrossRef
Google scholar
|
[12] |
Mañes S, Martínez-A C. Cholesterol domains regulate the actin cytoskeleton at the leading edge of moving cells. Trends in Cell Biology, 2004, 14(6): 275–278
CrossRef
Google scholar
|
[13] |
Sun M, Northup N, Marga F, Huber T, Byfield F J, Levitan I, Forgacs G. The effect of cellular cholesterol on membrane-cytoskeleton adhesion. Journal of Cell Science, 2007, 120(13): 2223–2231
CrossRef
Google scholar
|
[14] |
Norman L L, Oetama R J, Dembo M, Byfield F, Hammer D A, Levitan I, Aranda-Espinoza H. Modification of cellular cholesterol content affects traction force, adhesion and cell spreading. Cellular and Molecular Bioengineering, 2010, 3(2): 151–162
CrossRef
Google scholar
|
[15] |
Yang Y T, Liao J D, Lin C C K, Chang C T, Wang S H, Ju M S. Characterization of cholesterol-depleted or-restored cell membranes by depth-sensing nano-indentation. Soft Matter, 2012, 8(3): 682–687
CrossRef
Google scholar
|
[16] |
Kilbride P, Woodward H J, Tan K B, Thanh N T, Chu K E, Minogue S, Waugh M G. Modeling the effects of cyclodextrin on intracellular membrane vesicles from Cos-7 cells prepared by sonication and carbonate treatment. PeerJ, 2015, 3: e1351
CrossRef
Google scholar
|
[17] |
Zidovetzki R, Levitan I. Use of cyclodextrins to manipulate plasma membrane cholesterol content: Evidence, misconceptions and control strategies. Biochimica et Biophysica Acta (BBA)— Biomembranes, 2007, 1768(6): 1311–1324
CrossRef
Google scholar
|
[18] |
Christian A, Haynes M, Phillips M, Rothblat G. Use of cyclodextrins for manipulating cellular cholesterol content. Journal of Lipid Research, 1997, 38(11): 2264–2272
|
[19] |
Romanenko V G, Fang Y, Byfield F, Travis A J, Vandenberg C A, Rothblat G H, Levitan I. Cholesterol sensitivity and lipid raft targeting of Kir2. 1 channels. Biophysical Journal, 2004, 87(6): 3850–3861
CrossRef
Google scholar
|
[20] |
Mahammad S, Parmryd I. Cholesterol depletion using methyl--cyclodextrin. Methods in Membrane Lipids, 2015: 91–102
|
[21] |
Romanenko V G, Rothblat G H, Levitan I. Modulation of endothelial inward-rectifier K+ current by optical isomers of cholesterol. Biophysical Journal, 2002, 83(6): 3211–3222
CrossRef
Google scholar
|
[22] |
Levitan I, Christian A E, Tulenko T N, Rothblat G H. Membrane cholesterol content modulates activation of volume-regulated anion current in bovine endothelial cells. Journal of General Physiology, 2000, 115(4): 405–416
CrossRef
Google scholar
|
[23] |
Niu S L, Mitchell D C, Litman B J. Manipulation of cholesterol levels in rod disk membranes by methyl-β-cyclodextrin effects on receptor activation. Journal of Biological Chemistry, 2002, 277(23): 20139–20145
CrossRef
Google scholar
|
[24] |
Klein U, Gimpl G, Fahrenholz F. Alteration of the myometrial plasma membrane cholesterol content with β-cyclodextrin modulates the binding affinity of the oxytocin receptor. Biochemistry, 1995, 34(42): 13784–13793
CrossRef
Google scholar
|
[25] |
Roduit C, van der Goot F G, De Los Rios P, Yersin A, Steiner P, Dietler G, Catsicas S, Lafont F, Kasas S. Elastic membrane heterogeneity of living cells revealed by stiff nanoscale membrane domains. Biophysical Journal, 2008, 94(4): 1521–1532
CrossRef
Google scholar
|
[26] |
Bronder A M, Bieker A, Elter S, Etzkorn M, Häussinger D, Oesterhelt F. Oriented membrane protein reconstitution into tethered lipid membranes for AFM force spectroscopy. Biophysical Journal, 2016, 111(9): 1925–1934
CrossRef
Google scholar
|
[27] |
Casuso I, Khao J, Chami M, Paul-Gilloteaux P, Husain M, Duneau J P, Stahlberg H, Sturgis J N, Scheuring S. Characterization of the motion of membrane proteins using high-speed atomic force microscopy. Nature Nanotechnology, 2012, 7(8): 525–529
CrossRef
Google scholar
|
[28] |
Hutter J L, Bechhoefer J. Calibration of atomic-force microscope tips. Review of Scientific Instruments, 1993, 64(7): 1868–1873
CrossRef
Google scholar
|
[29] |
Sneddon I N. The relation between load and penetration in the axisymmetric Boussinesq problem for a punch of arbitrary profile. International Journal of Engineering Science, 1965, 3(1): 47–57
CrossRef
Google scholar
|
[30] |
Matzke R, Jacobson K, Radmacher M. Direct, high-resolution measurement of furrow stiffening during division of adherent cells. Nature Cell Biology, 2001, 3(6): 607–610
CrossRef
Google scholar
|
[31] |
Emad A, Heinz W F, Antonik M D, D’Costa N P, Nageswaran S, Schoenenberger C A, Hoh J H. Relative microelastic mapping of living cells by atomic force microscopy. Biophysical Journal, 1998, 74(3): 1564–1578
CrossRef
Google scholar
|
[32] |
Lam R S, Shaw A R, Duszyk M. Membrane cholesterol content modulates activation of BK channels in colonic epithelia. Biochimica et Biophysica Acta (BBA)— Biomembranes, 2004, 1667(2): 241–248
CrossRef
Google scholar
|
[33] |
Toselli M, Biella G, Taglietti V, Cazzaniga E, Parenti M. Caveolin-1 expression and membrane cholesterol content modulate N-type calcium channel activity in NG108-15 cells. Biophysical Journal, 2005, 89(4): 2443–2457
CrossRef
Google scholar
|
[34] |
Oh H, Mohler E R III, Tian A, Baumgart T, Diamond S L. Membrane cholesterol is a biomechanical regulator of neutrophil adhesion. Arteriosclerosis, Thrombosis, and Vascular Biology, 2009, 29(9): 1290–1297
CrossRef
Google scholar
|
[35] |
Corvera S, DiBonaventura C, Shpetner H S. Cell confluence-dependent remodeling of endothelial membranes mediated by cholesterol. Journal of Biological Chemistry, 2000, 275(40): 31414–31421
CrossRef
Google scholar
|
[36] |
Frankel D, Pfeiffer J, Surviladze Z, Johnson A, Oliver J, Wilson B, Burns A. Revealing the topography of cellular membrane domains by combined atomic force microscopy/fluorescence imaging. Biophysical Journal, 2006, 90(7): 2404–2413
CrossRef
Google scholar
|
[37] |
Kwik J, Boyle S, Fooksman D, Margolis L, Sheetz M P, Edidin M. Membrane cholesterol, lateral mobility, and the phosphatidylinositol 4,5-bisphosphate-dependent organization of cell actin. Proceedings of the National Academy of Sciences of the United States of America, 2003, 100(24): 13964–13969
CrossRef
Google scholar
|
[38] |
Byfield F J, Tikku S, Rothblat G H, Gooch K J, Levitan I. OxLDL increases endothelial stiffness, force generation, and network formation. Journal of Lipid Research, 2006, 47(4): 715–723
CrossRef
Google scholar
|
[39] |
Zhang X, Hurng J, Rateri D L, Daugherty A, Schmid-Schönbein G W, Shin H Y. Membrane cholesterol modulates the fluid shear stress response of polymorphonuclear leukocytes via its effects on membrane fluidity. American Journal of Physiology. Cell Physiology, 2011, 301(2): C451–C460
CrossRef
Google scholar
|
[40] |
Borbiev T, Radel C, Rizzo V. Participation of caveolae in β1 integrin-mediated mechanotransduction. FASEB Journal, 2007, 21(6): A752–A752
|
[41] |
Qi Y, Andolfi L, Frattini F, Mayer F, Lazzarino M, Hu J. Membrane stiffening by STOML3 facilitates mechanosensation in sensory neurons. Nature Communications, 2015, 6(1): 8512
CrossRef
Google scholar
|
[42] |
Byfield F J, Aranda-Espinoza H, Romanenko V G, Rothblat G H, Levitan I. Cholesterol depletion increases membrane stiffness of aortic endothelial cells. Biophysical Journal, 2004, 87(5): 3336–3343
CrossRef
Google scholar
|
[43] |
Hissa B, Pontes B, Roma P M S, Alves A P, Rocha C D, Valverde T M, Aguiar P H N, Almeida F P, Guimaraes A J, Guatimosim C,
CrossRef
Google scholar
|
[44] |
Brown R E. Sphingolipid organization in biomembranes: What physical studies of model membranes reveal. Journal of Cell Science, 1998, 111(1): 1–9
|
[45] |
Pralle A, Keller P, Florin E L, Simons K, Hörber J H. Sphingolipid-cholesterol rafts diffuse as small entities in the plasma membrane of mammalian cells. Journal of Cell Biology, 2000, 148(5): 997–1008
CrossRef
Google scholar
|
[46] |
Wakatsuki T, Schwab B, Thompson N C, Elson E L. Effects of cytochalasin D and latrunculin B on mechanical properties of cells. Journal of Cell Science, 2001, 114(5): 1025–1036
|
[47] |
Khatibzadeh N, Gupta S, Farrell B, Brownell W E, Anvari B. Effects of cholesterol on nano-mechanical properties of the living cell plasma membrane. Soft Matter, 2012, 8(32): 8350–8360
CrossRef
Google scholar
|
[48] |
Zhang L, Bennett W F D, Zheng T, Ouyang P K, Ouyang X P, Qiu X Q, Luo A Q, Karttunen M, Chen P. Effect of cholesterol on cellular uptake of cancer drugs pirarubicin and ellipticine. Journal of Physical Chemistry B, 2016, 120(12): 3148–3156
CrossRef
Google scholar
|
[49] |
Ramprasad O, Srinivas G, Rao K S, Joshi P, Thiery J P, Dufour S, Pande G. Changes in cholesterol levels in the plasma membrane modulate cell signaling and regulate cell adhesion and migration on fibronectin. Cytoskeleton, 2007, 64(3): 199–216
CrossRef
Google scholar
|
[50] |
López C A, de Vries A H, Marrink S J. Molecular mechanism of cyclodextrin mediated cholesterol extraction. PLoS Computational Biology, 2011, 7(3): e1002020
CrossRef
Google scholar
|
/
〈 | 〉 |