High resolution imaging of collagen organisation and synthesis using a versatile collagen specific probe.

Collagen is the protein primarily responsible for the load-bearing properties of tissues and collagen architecture is one of the main determinants of the mechanical properties of tissues. Visualisation of changes in collagen three-dimensional structure is essential in order to improve our understanding of collagen fibril formation and remodelling, e.g. in tissue engineering experiments. A recently developed collagen probe, based on a natural collagen binding protein (CNA35) conjugated to a fluorescent dye, showed to be much more specific to collagen than existing fluorescent techniques currently used for collagen visualisation in live tissues. In this paper, imaging with this fluorescent CNA35 probe was compared to imaging with second harmonic generation (SHG) and the imaging of two- and three-dimensional collagen organisation was further developed. A range of samples (cell culture, blood vessels and engineered tissues) was imaged to illustrate the potential of this collagen probe. This images of collagen organisation showed improved detail compared to images generated with SHG, which is currently the most effective method for viewing three-dimensional collagen organisation in tissues. In conclusion, the fluorescent CNA35 probe allows easy access to high resolution imaging of collagen, ranging from very young fibrils to more mature collagen fibres. Furthermore, this probe enabled real-time visualisation of collagen synthesis in cell culture, which provides new opportunities to study collagen synthesis and remodelling.

[1]  M. Sacks,et al.  Biaxial mechanical properties of the natural and glutaraldehyde treated aortic valve cusp--Part I: Experimental results. , 2000, Journal of biomechanical engineering.

[2]  Karsten König,et al.  Imaging of cardiovascular structures using near-infrared femtosecond multiphoton laser scanning microscopy. , 2005, Journal of biomedical optics.

[3]  Karsten König,et al.  Impact of cryopreservation on extracellular matrix structures of heart valve leaflets. , 2006, The Annals of thoracic surgery.

[4]  A. Pena,et al.  Micrometer scale Ex Vivo multiphoton imaging of unstained arterial wall structure , 2006, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

[5]  Benedicto de Campos Vidal,et al.  Image analysis of tendon helical superstructure using interference and polarized light microscopy. , 2003 .

[6]  B. Hinz,et al.  Mechanical tension controls granulation tissue contractile activity and myofibroblast differentiation. , 2001, The American journal of pathology.

[7]  Peter Fratzl,et al.  Cellulose and collagen: from fibres to tissues , 2003 .

[8]  R Gauderon,et al.  Optimization of second-harmonic generation microscopy. , 2001, Micron.

[9]  D. Slaaf,et al.  Two-Photon Microscopy of Vital Murine Elastic and Muscular Arteries , 2006, Journal of Vascular Research.

[10]  Z. Galis,et al.  Quantitative assessment of collagen assembly by live cells. , 2003, Journal of biomedical materials research. Part A.

[11]  Watt W Webb,et al.  Interpreting second-harmonic generation images of collagen I fibrils. , 2005, Biophysical journal.

[12]  M. Sacks,et al.  Biaxial mechanical properties of the native and glutaraldehyde-treated aortic valve cusp: Part II--A structural constitutive model. , 2000, Journal of biomechanical engineering.

[13]  Peter Friedl,et al.  Confocal reflection imaging of 3D fibrin polymers. , 2006, Blood cells, molecules & diseases.

[14]  Marcel C. M. Rutten,et al.  Tissue Engineering of Human Heart Valve Leaflets: A Novel Bioreactor for a Strain-Based Conditioning Approach , 2005, Annals of Biomedical Engineering.

[15]  B. Tromberg,et al.  Imaging cells and extracellular matrix in vivo by using second-harmonic generation and two-photon excited fluorescence , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[16]  W. Webb,et al.  Live tissue intrinsic emission microscopy using multiphoton-excited native fluorescence and second harmonic generation , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Iris Riemann,et al.  High-resolution multiphoton tomography of human skin with subcellular spatial resolution and picosecond time resolution. , 2003, Journal of biomedical optics.

[18]  Peter Friedl,et al.  Functional imaging of pericellular proteolysis in cancer cell invasion. , 2005, Biochimie.

[19]  Andras Czirok,et al.  Elastic fiber formation: A dynamic view of extracellular matrix assembly using timer reporters , 2006, Journal of cellular physiology.

[20]  J. P. Robinson,et al.  Time-lapse confocal reflection microscopy of collagen fibrillogenesis and extracellular matrix assembly in vitro. , 2000, Biopolymers.

[21]  J. Paul Robinson,et al.  Three-dimensional imaging of extracellular matrix and extracellular matrix-cell interactions. , 2001, Methods in cell biology.

[22]  F J Schoen,et al.  Functional Living Trileaflet Heart Valves Grown In Vitro , 2000, Circulation.

[23]  Tatsuo Ushiki,et al.  Collagen fibers, reticular fibers and elastic fibers. A comprehensive understanding from a morphological viewpoint. , 2002, Archives of histology and cytology.

[24]  Maarten Merkx,et al.  Fluorescently labeled collagen binding proteins allow specific visualization of collagen in tissues and live cell culture. , 2006, Analytical biochemistry.

[25]  D. Slaaf,et al.  Imaging Collagen in Intact Viable Healthy and Atherosclerotic Arteries Using Fluorescently Labeled CNA35 and Two-Photon Laser Scanning Microscopy , 2007, Molecular imaging.

[26]  K. König,et al.  Multiphoton autofluorescence imaging of intratissue elastic fibers. , 2005, Biomaterials.

[27]  P. Meneton,et al.  Uterine Artery Structural and Functional Changes During Pregnancy in Tissue Kallikrein–Deficient Mice , 2003, Arteriosclerosis, thrombosis, and vascular biology.

[28]  L. Niklason,et al.  Effects of Copper and Cross-Linking on the Extracellular Matrix of Tissue-Engineered Arteries , 2005, Cell transplantation.

[29]  Bruce J Tromberg,et al.  Imaging coronary artery microstructure using second-harmonic and two-photon fluorescence microscopy. , 2004, Biophysical journal.

[30]  Andras Czirok,et al.  Elastic fiber macro‐assembly is a hierarchical, cell motion‐mediated process , 2006, Journal of cellular physiology.

[31]  E. Sevick-Muraca,et al.  Quantitative optical spectroscopy for tissue diagnosis. , 1996, Annual review of physical chemistry.

[32]  D. Slaaf,et al.  Two-Photon Microscopy for Imaging of the (Atherosclerotic) Vascular Wall: A Proof of Concept Study , 2004, Journal of Vascular Research.

[33]  Guy Cox,et al.  3-dimensional imaging of collagen using second harmonic generation. , 2003, Journal of structural biology.

[34]  J Mertz,et al.  Coherent scattering in multi-harmonic light microscopy. , 2001, Biophysical journal.

[35]  R. Sodian,et al.  Optimal cell source for cardiovascular tissue engineering: venous vs. aortic human myofibroblasts. , 2001, The Thoracic and cardiovascular surgeon.

[36]  H. Lodish Molecular Cell Biology , 1986 .

[37]  S. Narayana,et al.  A ‘Collagen Hug’ Model for Staphylococcus aureus CNA binding to collagen , 2005, The EMBO journal.

[38]  C. Oomens,et al.  The Relative Contributions of Compression and Hypoxia to Development of Muscle Tissue Damage: An In Vitro Study , 2007, Annals of Biomedical Engineering.

[39]  William A Mohler,et al.  Three-dimensional high-resolution second-harmonic generation imaging of endogenous structural proteins in biological tissues. , 2002, Biophysical journal.

[40]  James V Jester,et al.  Dynamic three-dimensional visualization of collagen matrix remodeling and cytoskeletal organization in living corneal fibroblasts. , 2006, Scanning.