單細(xì)胞牽張拉伸壓縮形變與機(jī)械力特性測(cè)試分析系統(tǒng)

——基于微流控技術(shù)的單細(xì)胞機(jī)械力特性精準(zhǔn)、高通量表征 
Single cell mechanics - the easy way 
 
背景： 
單細(xì)胞水平的機(jī)械力特性表征，可以有效闡明細(xì)胞的功能和狀態(tài)，揭示細(xì)胞的單體差異性，對(duì)于細(xì)胞的分化和病理研究，以及**的早期臨床診斷和**具有非常重要的意義。 該系統(tǒng)基于微流控芯片的方式更適合單細(xì)胞樣本的微環(huán)境**控制、高通量定向操縱及多參數(shù)非特異性檢測(cè)。 
簡(jiǎn)介： 
該單細(xì)胞高通量牽張與力學(xué)特性測(cè)試分析系統(tǒng),是****臺(tái)用來(lái)高通量測(cè)量、分析單個(gè)懸浮細(xì)胞形變的設(shè)備。用來(lái)可視化研究討論細(xì)胞力學(xué)性質(zhì)與其功能之間的關(guān)系 該系統(tǒng)可以安裝在任何相位差顯微鏡上的模塊。溫度穩(wěn)定和激光**。 
  

系統(tǒng)亮點(diǎn)特性： 
1 ）可大量表征單細(xì)胞機(jī)械力特性、操作簡(jiǎn)便、樣品消耗量小 
該系統(tǒng)的微流控芯片具有與細(xì)胞直徑良好相符性的微納米級(jí)腔道，并能實(shí)現(xiàn)對(duì)微流體的**控制，使其尤其適合單細(xì)胞機(jī)械特性研究分析，該微流控的高通量技術(shù)便于大量表征單細(xì)胞機(jī)械力特性、操作簡(jiǎn)便、樣品消耗量小、集成和微型化程度高等優(yōu)點(diǎn)，且在分析過(guò)程中單細(xì)胞懸浮高速流經(jīng)檢測(cè)區(qū)域，該連續(xù)流動(dòng)態(tài)檢測(cè)的特性*大提高了系統(tǒng)的通量。 
2）高速對(duì)單個(gè)細(xì)胞進(jìn)行形變，并進(jìn)行機(jī)械特性高速表征，單細(xì)胞高通量流變 
利用兩素未聚焦光進(jìn)行單細(xì)胞形變，并通過(guò)圖形化微柱基地表征細(xì)胞的力特性,高速有效分析單細(xì)胞水平的機(jī)械特性, 高達(dá)300個(gè)細(xì)胞/小時(shí). 
3）非機(jī)械接觸、無(wú)標(biāo)記進(jìn)行細(xì)胞捕捉和拉伸，確保細(xì)胞**與細(xì)胞損傷*小化(Contact-free cell deformation)
利用光延伸器技術(shù)測(cè)試細(xì)胞機(jī)械特性能時(shí)，在非機(jī)械接觸情況下細(xì)胞進(jìn)行捕捉和拉伸，且不需要對(duì)激光進(jìn)行聚焦，能實(shí)現(xiàn)細(xì)胞損傷*小化。優(yōu)于AFM（原子力顯微鏡）和光鑷 
4）將光延伸器**性與微流控高通量**相結(jié)合，細(xì)胞機(jī)械特性測(cè)試分析**而且高效 
采用2個(gè)微流道來(lái)輸送細(xì)胞，使兩條光纖垂直分布于通道兩側(cè)并嚴(yán)格對(duì)準(zhǔn)? ，單細(xì)胞隨流體進(jìn)入檢測(cè)區(qū)域時(shí)，首先采用功率較低的光速捕獲細(xì)胞，然后增加光速的功率使細(xì)胞發(fā)生形變。通過(guò)對(duì)細(xì)胞變形能力的分析，不僅能區(qū)分病變細(xì)胞和正常細(xì)胞，而且可以用于辨別轉(zhuǎn)型特性和非轉(zhuǎn)移特性的癌細(xì)胞。 
5)自動(dòng)化測(cè)量單細(xì)胞力屬性和成像記錄細(xì)胞形變記錄 
對(duì)應(yīng)于用戶(hù)定義的拉伸模式，細(xì)胞被自動(dòng)傳送到測(cè)量區(qū)域由CellStretcher模塊控制所有組件和自動(dòng)測(cè)量細(xì)胞；細(xì)胞形變由系統(tǒng)CCD相機(jī)自動(dòng)記錄，并由CellEvaluator自動(dòng)提取記錄顯微圖像形變數(shù)據(jù)，CellReporter可視化統(tǒng)計(jì)分析表征參數(shù)。在光學(xué)拉伸加載運(yùn)行實(shí)驗(yàn)中，科研學(xué)者可專(zhuān)注于闡述實(shí)驗(yàn)結(jié)果 
6)良好溫控微環(huán)境罩 

Publications

RS ZELLTECHNIK BROCHURES

The Optical Stretcher

OPTICAL STRETCHER TECHNOLOGY

Lincoln, B., Schinkinger, S., Travis, K., Wottawah, F., Ebert, S., Sauer, F., Guck, J., 2007. Reconfigurable microfluidic integration of a dual-beam laser trap with biomedical applications. Biomed. Microdevices 9, 703–710. doi:10.1007/s10544-007-9079-x
Ebert, S., Travis, K., Lincoln, B., Guck, J., 2007. Fluorescence ratio thermometry in a microfluidic dual-beam laser trap. Opt. Express 15, 15493–15499. doi:10.1364/OE.15.015493
Jensen-McMullin, C., Lee, H.P., Lyons, E.R.L., 2005. Demonstration of trapping, motion control, sensing and fluorescence detection of polystyrene beads in a multi-fiber optical trap. Opt. Express 13, 2634–2642. doi:10.1364/OPEX.13.002634
Wottawah, F., Schinkinger, S., Lincoln, B., Ananthakrishnan, R., Romeyke, M., Guck, J., K?s, J., 2005. Optical Rheology of Biological Cells. Phys. Rev. Lett. 94, 098103. doi:10.1103/PhysRevLett.94.098103
Lincoln, B., Erickson, H.M., Schinkinger, S., Wottawah, F., Mitchell, D., Ulvick, S., Bilby, C., Guck, J., 2004. Deformability-based flow cytometry.Cytometry A 59A, 203–209. doi:10.1002/cyto.a.20050

THEORETICAL MODELS

Ananthakrishnan, R., Guck, J., Wottawah, F., Schinkinger, S., Lincoln, B., Romeyke, M., Kas, J., 2005. Modelling the structural response of an eukaryotic cell in the optical stretcher. Curr. Sci. 88.
B. Bareil, P., Sheng, Y., Chiou, A., 2006. Local scattering stress distribution on surface of a spherical cell in optical stretcher. Opt. Express 14, 12503–12509. doi:10.1364/OE.14.012503 
Bareil, P.B., Sheng, Y., Chen, Y.-Q., Chiou, A., 2007. Calculation of spherical red blood cell deformation in a dual-beam optical stretcher. Opt. Express 15, 16029–16034. doi:10.1364/OE.15.016029 
Boyde, L., Ekpenyong, A., Whyte, G., Guck, J., 2012. Comparison of stresses on homogeneous spheroids in the optical stretcher computed with geometrical optics and generalized Lorenz–Mie theory. Appl. Opt. 51, 7934–7944. doi:10.1364/AO.51.007934
Ekpenyong, A.E., Posey, C.L., Chaput, J.L., Burkart, A.K., Marquardt, M.M., Smith, T.J., Nichols, M.G., 2009. Determination of cell elasticity through hybrid ray optics and continuum mechanics modeling of cell deformation in the optical stretcher. Appl. Opt. 48, 6344–6354. doi:10.1364/AO.48.006344
Teo, S.-K., Goryachev, A.B., Parker, K.H., Chiam, K.-H., 2010. Cellular deformation and intracellular stress propagation during optical stretching.Phys. Rev. E 81, 051924. doi:10.1103/PhysRevE.81.051924

CANCER RESEARCH AND DIAGNOSTICS

Kastl, L., Budde, B., Isbach, M., Rommel, C., Kemper, B., Schnekenburger, J., 2015. Optomechanical properties of cancer cells revealed by light-induced deformation and quantitative phase microscopy. pp. 952908–952908–6. doi:10.1117/12.2184764
Martin, M., Müller, K., Cadenas, C., Hermes, M., Zink, M., Hengstler, J.G., K?s, J.A., 2012. ERBB2 overexpression triggers transient high mechanoactivity of breast tumor cells. Cytoskeleton 69, 267–277. doi:10.1002/cm.21023
Fritsch, A., H?ckel, M., Kiessling, T., Nnetu, K.D., Wetzel, F., Zink, M., K?s, J.A., 2010. Are biomechanical changes necessary for tumour progression? Nat. Phys. 6, 730–732. doi:10.1038/nphys1800
Brunner, C., Niendorf, A., K?s, J.A., 2009. Passive and active single-cell biomechanics: a new perspective in cancer diagnosis. Soft Matter 5, 2171–2178. doi:10.1039/B807545J
Remmerbach, T.W., Wottawah, F., Dietrich, J., Lincoln, B., Wittekind, C., Guck, J., 2009. Oral Cancer Diagnosis by Mechanical Phenotyping. Cancer Res. 69, 1728–1732. doi:10.1158/0008-5472.CAN-08-4073
Martin, M., Mueller, K., Wottawah, F., Schinkinger, S., Lincoln, B., Romeyke, M., K?s, J.A., 2006. Feeling with light for cancer. p. 60800P–60800P–10. doi:10.1117/12.637899
Guck, J., Schinkinger, S., Lincoln, B., Wottawah, F., Ebert, S., Romeyke, M., Lenz, D., Erickson, H.M., Ananthakrishnan, R., Mitchell, D., K?s, J., Ulvick, S., Bilby, C., 2005. Optical Deformability as an Inherent Cell Marker for Testing Malignant Transformation and Metastatic Competence. Biophys. J. 88, 3689–3698. doi:10.1529/biophysj.104.045476 

STEM CELL RESEARCH

Ekpenyong, A.E., Whyte, G., Chalut, K., Pagliara, S., Lautenschlaeger, F., Fiddler, C., Paschke, S., Keyser, U.F., Chilvers, E.R., Guck, J., 2012.Viscoelastic Properties of Differentiating Blood Cells Are Fate- and Function-Dependent. Plos One 7, e45237. doi:10.1371/journal.pone.0045237
Galle, J., Bader, A., Hepp, P., Grill, W., Fuchs, B., Kas, J.A., Krinner, A., MarquaB, B., Muller, K., Schiller, J., Schulz, R.M., von Buttlar, M., von der Burg, E., Zscharnack, M., Loffler, M., 2010. Mesenchymal Stem Cells in Cartilage Repair: State of the Art and Methods to monitor Cell Growth, Differentiation and Cartilage Regeneration. Curr. Med. Chem. 17, 2274–2291. doi:10.2174/092986710791331095
Maloney, J.M., Nikova, D., Lautenschlager, F., Clarke, E., Langer, R., Guck, J., Van Vliet, K.J., 2010. Mesenchymal Stem Cell Mechanics from the Attached to the Suspended State. Biophys. J. 99, 2479–2487. doi:10.1016/j.bpj.2010.08.052
Lautenschl?ger, F., Paschke, S., Schinkinger, S., Bruel, A., Beil, M., Guck, J., 2009. The regulatory role of cell mechanics for migration of differentiating myeloid cells. Proc. Natl. Acad. Sci. 106, 15696–15701 doi:10.1073/pnas.0811261106

IMMUNE SYSTEM

Man, S.M., Ekpenyong, A., Tourlomousis, P., Achouri, S., Cammarota, E., Hughes, K., Rizzo, A., Ng, G., Wright, J.A., Cicuta, P., Guck, J.R., Bryant, C.E., 2014. Actin polymerization as a key innate immune effector mechanism to control Salmonella infection. Proc. Natl. Acad. Sci. 201419925 doi:10.1073/pnas.1419925111

BASIC RESEARCH

Schmidt, B.U.S., Kie?ling, T.R., Warmt, E., Fritsch, A.W., Stange, R., K?s, J.A., 2015. Complex thermorheology of living cells. New J. Phys. 17, 073010. doi:10.1088/1367-2630/17/7/073010
Chan, C.J., Ekpenyong, A.E., Golfier, S., Li, W., Chalut, K.J., Otto, O., Elgeti, J., Guck, J., Lautenschl?ger, F., 2015. Myosin II Activity Softens Cells in Suspension. Biophys. J. 108, 1856–1869. doi:10.1016/j.bpj.2015.03.009
Gladilin, E., Gonzalez, P., Eils, R., 2014. Dissecting the contribution of actin and vimentin intermediate filaments to mechanical phenotype of suspended cells using high-throughput deformability measurements and computational modeling. J. Biomech. 47, 2598–2605. doi:10.1016/j.jbiomech.2014.05.020
Maloney, J.M., Vliet, K.J.V., 2014. Chemoenvironmental modulators of fluidity in the suspended biological cell. Soft Matter. doi:10.1039/C4SM00743C
Warmt, E., Kie?ling, T.R., Stange, R., Fritsch, A.W., Zink, M., K?s, J.A., 2014. Thermal instability of cell nuclei. New J. Phys. 16, 073009. doi:10.1088/1367-2630/16/7/073009
Gyger, M., Stange, R., Kiessling, T.R., Fritsch, A., Kostelnik, K.B., Beck-Sickinger, A.G., Zink, M., Kaes, J.A., 2014. Active contractions in single suspended epithelial cells. Eur. Biophys. J. Biophys. Lett. 43, 11–23. doi:10.1007/s00249-013-0935-8
Seltmann, K., Fritsch, A.W., K?s, J.A., Magin, T.M., 2013. Keratins significantly contribute to cell stiffness and impact invasive behavior. Proc. Natl. Acad. Sci. 201310493. doi:10.1073/pnas.1310493110
Maloney, J.M., Lehnhardt, E., Long, A.F., Van Vliet, K.J., 2013. Mechanical fluidity of fully suspended biological cells. Biophys. J. 105, 1767–1777. doi:10.1016/j.bpj.2013.08.040
Kie?ling, T.R., Stange, R., K?s, J.A., Fritsch, A.W., 2013. Thermorheology of living cells—impact of temperature variations on cell mechanics. New J. Phys. 15, 045026. doi:10.1088/1367-2630/15/4/045026
Kie?ling, T.R., Herrera, M., Nnetu, K.D., Balzer, E.M., Girvan, M., Fritsch, A.W., Martin, S.S., K?s, J.A., Losert, W., 2013. Analysis of multiple physical parameters for mechanical phenotyping of living cells. Eur. Biophys. J. 42, 383–394. doi:10.1007/s00249-013-0888-y
Paschke, S., Weidner, A.F., Paust, T., Marti, O., Beil, M., Ben-Chetrit, E., 2013. Technical advance: Inhibition of neutrophil chemotaxis by colchicine is modulated through viscoelastic properties of subcellular compartments. J. Leukoc. Biol. 94, 1091–1096. doi:10.1189/jlb.1012510
Chalut, K.J., H?pfler, M., Lautenschl?ger, F., Boyde, L., Chan, C.J., Ekpenyong, A., Martinez-Arias, A., Guck, J., 2012. Chromatin decondensation and nuclear softening accompany Nanog downregulation in embryonic stem cells. Biophys. J. 103, 2060–2070. doi:10.1016/j.bpj.2012.10.015
Matthews, H.K., Delabre, U., Rohn, J.L., Guck, J., Kunda, P., Baum, B., 2012. Changes in Ect2 localization couple actomyosin-dependent cell shape changes to mitotic progression. Dev. Cell 23, 371–383. doi:10.1016/j.devcel.2012.06.003
Mauritz, J.M.A., Esposito, A., Tiffert, T., Skepper, J.N., Warley, A., Yoon, Y.-Z., Cicuta, P., Lew, V.L., Guck, J.R., Kaminski, C.F., 2010. Biophotonic techniques for the study of malaria-infected red blood cells. Med. Biol. Eng. Comput. 48, 1055–1063. doi:10.1007/s11517-010-0668-0
Rusciano, G., 2010. Experimental analysis of Hb oxy–deoxy transition in single optically stretched red blood cells. Phys. Med. 26, 233–239. doi:10.1016/j.ejmp.2010.02.001

AGING PROCESSES

Schulze, C., Wetzel, F., Kueper, T., Malsen, A., Muhr, G., Jaspers, S., Blatt, T., Wittern, K.-P., Wenck, H., K?s, J.A., 2010. Stiffening of Human Skin Fibroblasts with Age. Biophys. J. 99, 2434–2442. doi:10.1016/j.bpj.2010.08.026

VESICLES

Delabre, U., Feld, K., Crespo, E., Whyte, G., Sykes, C., Seifert, U., Guck, J., 2015. Deformation of phospholipid vesicles in an optical stretcher. Soft Matter. doi:10.1039/C5SM00562K
Solmaz, M.E., Sankhagowit, S., Biswas, R., Mejia, C.A., Povinelli, M.L., Malmstadt, N., 2013. Optical stretching as a tool to investigate the mechanical properties of lipid bilayers. Rsc Adv. 3, 16632–16638. doi:10.1039/c3ra42510j 
Solmaz, M.E., Biswas, R., Sankhagowit, S., Thompson, J.R., Mejia, C.A., Malmstadt, N., Povinelli, M.L., 2012. Optical stretching of giant unilamellar vesicles with an integrated dual-beam optical trap. Biomed. Opt. Express 3, 2419–2427. doi:10.1364/BOE.3.002419

TECHNICAL ADVANCES

Grosser, S., Fritsch, A.W., Kie?ling, T.R., Stange, R., K?s, J.A., 2015. The lensing effect of trapped particles in a dual-beam optical trap. Opt. Express 23, 5221–5235. doi:10.1364/OE.23.005221
Bellini, N., Bragheri, F., Cristiani, I., Guck, J., Osellame, R., Whyte, G., 2012. Validation and perspectives of a femtosecond laser fabricated monolithic optical stretcher. Biomed. Opt. Express 3, 2658–2668. doi:10.1364/BOE.3.002658 
Bellini, N., Vishnubhatla, K.C., Bragheri, F., Ferrara, L., Minzioni, P., Ramponi, R., Cristiani, I., Osellame, R., 2010. Femtosecond laser fabricated monolithic chip for optical trapping and stretching of single cells. Opt. Express 18, 4679–4688. doi:10.1364/OE.18.004679