Structural organization of collagen fibers in chordae tendineae as assessed by optical anisotropic properties and Fast Fourier transform

Journal of Structural Biology

Volumn 167, Issue 2, 2009, Pages 166-175

  de Campos Vidal, Benedicto ^a   Mello, Maria Luiza S ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

Author keywords

Birefringence; Chordae tendineae; Collagen fibers; Crimp; FFT; Optical anisotropy

Indexed keywords

COLLAGEN FIBER;

ANIMAL TISSUE; ANISOTROPY; ARTICLE; BIREFRINGENCE; CHORDA TENDINEA; CONTROLLED STUDY; FOURIER TRANSFORMATION; IMAGE ANALYSIS; MALE; NONHUMAN; POLARIZATION MICROSCOPY; PRIORITY JOURNAL; SWINE; THREE DIMENSIONAL IMAGING; TISSUE DISTRIBUTION; TISSUE STRUCTURE;

ANIMALS; ANISOTROPY; CHORDAE TENDINEAE; COLLAGEN; FOURIER ANALYSIS; IMAGE PROCESSING, COMPUTER-ASSISTED; MICROSCOPY, POLARIZATION; PROTEIN CONFORMATION; SWINE;

SUS;

EID: 67649846307     PISSN: 10478477     EISSN: 10958657     Source Type: Journal    
DOI: 10.1016/j.jsb.2009.05.004     Document Type: Article

References (68)

1. Akhtar S., Meek K.M., and James V. Ultrastructure abnormalities in proteoglycans, collagen fibrils, and elastic fibers in normal and mixomatous mitral valve chordae tendineae. Cardiovasc. Pathol. 8 (1999) 191-201
2. Athenstaedt H. Pyroelectric and piezoelectric properties of vertebrates. Ann. NY Acad. Sci. 238 (1974) 68-94
3. Ayres C., Bowlin G.L., Henderson S.C., Taylor L., Shultz J., Alexander J., Telemeco T.A., and Simpson D.G. Modulation of anisotropy in electrospun tissue-engineering scaffolds: analysis of fiber alignment by the fast Fourier transform. Biomaterials 37 (2006) 5524-5534
4. Beche B., and Gaviot E. Matrix formalism to enhance the concept of effective dielectric constant. Opt. Commun. 219 (2003) 15-19
5. Benjamin M., and Ralphs J.R. Tendons and ligaments - an overview. Histol. Histopathol. 12 (1997) 1135-1144
6. Berendsen H.J., and Michelsen C. Hydration structure of fibrous macromolecules. Ann. NY Acad. Sci. 125 (1965) 365-379
7. Bi X., Li G., Doty S.B., and Camacho N.P. A novel method for determination of collagen orientation in cartilage by Fourier transform infrared imaging spectroscopy (FT-IRIS). Osteoarthritis Cartilage 13 (2005) 1050-1058
8. Boskey A., and Camacho N.P. FT-IR imaging of native and tissue-engineered bone and cartilage. Biomaterials 28 (2007) 2465-2478
9. Bozek L., van der Heijden G., and Horton M. Collagen fibrils: nanoscale ropes. Biophys. J. 92 (2007) 70-75
10. Cacho F., Elbischger P.J., Rodriguez J.F., Doblare M., and Holzapfel G.A. A constitutive model for fibrous tissues considering collagen fibre crimp. Int. J. Non-Linear Mech. 42 (2007) 391-402
11. Chaudhuri S., Nguyen H., Rangayyan R.M., Walsh S., and Frank C.B. A Fourier domain directional filtering method for analysis of collagen alignment in ligaments. IEEE Trans. Biomed. Eng. 34 (1987) 509-518
12. Cheng V.W.T., and Screen H.R.C. The micro-structural strain response of tendon. J. Mater. Sci. 42 (2007) 8957-8965
13. Cochran R.P., and Kunzelman K.S. Comparison of viscoelastic properties of suture versus porcine mitral-valve chordae tendineae. J. Card. Surg. 6 (1991) 508-513
14. Cornelissen J.J.L.M., Fischer M., Sommerdijk N.A.J.M., and Nolte R.J.M. Helical superstructures from charged poly(styrene)-poly(isocyanopeptide) block copolymers. Science 280 (1998) 1427-1430
15. de Vries H.J.C., Enomoto D.N.H., van Marle J., van Zuijlen P.P.M., Mekkes J.R., and Bos J.D. Dermal organization in scleroderma: the fast Fourier transform and the laser scatter method objectify fibrosis in nonlesional as well as lesional skin. Lab. Invest. 80 (2000) 1281-1289
16. Eriksson C. Electrical properties of bone. In: Bourne G.H. (Ed). The Biochemistry of Bone vol. 4 (1976), Academic Press, New York 329-384
17. Fukada E. Piezoelectric properties of organic polymers. Ann. NY Acad. Sci. 238 (1974) 7-25
18. Ghoreishi S.R., Cartraud P., Davies P., and Messager T. Analytical modeling of synthetic fiber ropes subjected to axial loads. Part I. A new continuum model for multilayered fibrous structures. Int. J. Solids Struct. 44 (2007) 2924-2942
19. Golovan L.A., Ivanov D.A., Melnikov V.A., Timoshenko V.Y., Zheltikov A.M., Kashkarov P.K., Petrov G.I., and Yakovlev V.V. Form birefringence of oxidized porous silicon. Appl. Phys. Lett. 88 (2006) 241113 10.1063/1.2212534
20. Grande-Allen K.J., Calabro A., Gupta V., Wight T.N., Hascall V.C., and Vesely I. Glycosaminoglycans and proteoglycans in normal mitral valve leaflets and chordae: association with regions of tensile and compressive loading. Glycobiology 14 (2004) 621-633
21. Grigera J.R., and Berendsen H.J.C. Molecular details of collagen hydration. Biopolymers 18 (1979) 47-57
22. Hamza A.A., Sokkar T.Z.N., El-Farahaty K.A., and El-Dessouky H.M. Determination of the intrinsic birefringence of polymeric fibres. Polymer Test. 23 (2004) 203-208
23. Harris C.M. The Fourier analysis of biological transients. J. Neurosci. Methods 83 (1998) 15-34
24. Heller W. Polarimetry. In: Weissberger A. (Ed). Physical Methods of Organic Chemistry Part III (1960), Intersci. Publ., Inc., New York 2147-2333
25. Icardo J.M., and Colvee E. Atrioventricular valves of the mouse: 3. Collagenous skeleton and myotendinous junction. Anat. Rec. 243 (1995) 367-375
26. Intrigila B., Melatti I., Tofani A., and Macchiarelli G. Computational models of myocardial endomysial collagen arrangement. Comput. Methods Programs Biomed. 86 (2007) 232-244
27. Inoué S. Video image-processing greatly enhances contrast, quality, and speed in polarization-based microscopy. J. Cell Biol. 89 (1981) 346-356
28. Jaworek T., Neher D., Wegner G., Wieringa R.H., and Schouten A.J. Electromechanical properties of an ultrathin layer of directionally aligned helical polypeptides. Science 279 (1978) 57-60
29. Kim B.M., Eichler J., Reiser K.M., Rubenchik A.M., and Da Silva L.B. Collagen structure and nonlinear susceptibility: effects of heat, glycation, and enzymatic cleavage on second harmonic signal intensity. Laser Surg. Med. 27 (2000) 329-335
30. Krasnosselskaia L.V., Fullerton G.D., Dodd S.J., and Cameron I.L. Water in tendon: orientational analysis of the free induction decay. Magn. Reson. Med. 54 (2005) 280-288
31. Leech C.M. The modelling of friction in polymer fibre ropes. Int. J. Mech. Sci. 44 (2002) 621-643
32. Lehn J.M. Supramolecular polymer chemistry - scope and perspectives. Polymer Int. 51 (2002) 825-839
33. Liao J., and Vesely I. A structural basis for the size-related mechanical properties of mitral valve chordae tendineae. J. Biomech. 36 (2003) 1125-1133
34. Liao J., and Vesely I. Skewness angle of interfibrillar proteoglycans increases with applied load on mitral valve chordae tendineae. J. Biomech. 40 (2007) 390-398
35. Lim K.O., and Boughner D.R. Morphology and relationship to extensibility curves of mitral-valve chordae tendineae. Circ. Res. 39 (1976) 580-585
36. Mello M.L.S., Godo C., Vidal B.C., and Abujadi J.M. Changes in the macromolecular orientation on collagen fibers during the process of tendon repair in the rat. Ann. Histochim. 20 (1975) 145-152
37. Mello M.L.S., Vidal B.C., de Carvalho A.C., and Caseiro-Filho A.C. Change with age of anisotropic properties of collagen. Gerontology 25 (1979) 2-8
38. Millington-Sanders C., Meir A., Lawrence L., and Stolinski C. Structure of chordae tendineae in the left ventricle of the human heart. J. Anat. 192 (1998) 573-581
39. Neale S.L., Macdonald M.P., Dholakia K., and Krauss T.F. All-optical control of microfluidic components using form birefringence. Nat. Mater. 4 (2005) 530-533
40. O B.H., Choi C.H., Jo S.B., Lee M.W., Park D.G., Kang B.G., Kim S.H., Liu R., Li Y.Y., Sailor M.J., and Fainman Y. Novel form birefringence modeling for an ultracompact sensor in porous silicon films using polarization interferometry. IEEE Photon. Technol. Lett. 16 (2004) 1546-1548
41. Ourmazd A., Taylor D.W., Bode M., and Kim Y. Quantifying the information-content of lattice images. Science 246 (1989) 1571-1577
42. Pang L., Nezhad M., Levy U., Tsai C.H., and Fainman Y. Form-birefringence structure fabrication in GaAs by use of SU-8 as a dry-etching mask. Appl. Opt. 44 (2005) 2377-2381
43. Pena A.M., Boulesteix T., Dartigalongue T., and Schanne-Klein M.C. Chiroptical effects in the second harmonic signal of collagens I and IV. J. Am. Chem. Soc. 127 (2005) 10314-10322
44. Rebel, G., Verreet, R., Ridge, I.M.L., 2006. Lightweight ropes for lifting applications. In: OIPEEC Conference - Athens, 2006, pp. 33-54. Available from: www.ropetechnology.com/bro_engl/lightweight_ropes.pdf.
45. Ritchie J., Jimenez J., He Z.M., Sacks M.S., and Yoganathan A.P. The material properties of the native porcine mitral valve chordae tendineae: an in vitro investigation. J. Biomech. 39 (2006) 1129-1135
46. Roth S., and Freund I. Optical second-harmonic scattering in rat-tail tendon. Biopolymers 20 (1981) 1271-1290
47. Roth S., and Freund I. Second-harmonic generation and orientational order in connective tissue: a mosaic model for fibril orientational ordering in rat-tail tendon. J. Appl. Cryst. 15 (1982) 72-78
48. Sato I. Coil-like structure of the inner core of chordae tendineae. Clin. Anat. 15 (2002) 196-198
49. Silver D., Miller J., Harrison R., and Prockop D.J. Helical model of nucleation and propagation to account for the growth of type I collagen fibrils from symmetrical pointed tips: a special example of self-assembly of rod-like monomers. Proc. Natl. Acad. Sci. USA 89 (1992) 9860-9864
50. Silver F.H., and Siperko L.M. Mechanosensing and mechanochemical transduction: how is mechanical energy sensed and converted into chemical energy in an extracellular matrix?. Crit. Rev. Biomed. Eng. 31 (2003) 255-331
51. Vasanthan N. Determination of molecular orientation of uniaxially stretched polyamide fibers by polarized infrared spectroscopy: comparison of X-ray diffraction and birefringence methods. Appl. Spectrosc. 59 (2005) 897-903
52. Verbiest T., Van Elshocht S., Kauranen M., Hellemans L., Snauwaert J., Nuckolls C., Katz T.J., and Persoons A. Strong enhancement of nonlinear optical properties through supramolecular chirality. Science 282 (1998) 913-915
53. Vidal B.C. The part played by the mucopolysaccharides in the form birefringence of collagen. Protoplasma 59 (1964) 472-479
54. Vidal B.C. Interferometric and histochemical investigation on collagen bundles: refractive index and dry masses prior and after staining with orange G. Ann. Histochim. 15 (1970) 191-205
55. Vidal B.C. Acid glycosaminoglycans and endochondral ossification: microspectrophotometric evaluation and macromolecular orientation. Cell. Mol. Biol. 22 (1977) 45-64
56. Vidal B.C. The part played by proteoglycans and structural glycoproteins in the macromolecular orientation of collagen bundles. Cell. Mol. Biol. 26 (1980) 415-421
57. Vidal B.C. Evaluation of the carbohydrate role in the molecular order of collagen bundles. Microphotometric measurements of textural birefringence. Cell. Mol. Biol. 32 (1986) 527-535
58. Vidal B.C. Crimp as part of a helical structure. C. R. Acad. Sci. Paris Sci. Vie/Life Sci. 318 (1995) 173-178
59. Vidal B.C. Image analysis of tendon helical superstructure using interference and polarized light microscopy. Micron 34 (2003) 423-432
60. Vidal B.C., and Mello M.L.S. Chirality and helicity of poly-l-benzyl-glutamate in liquid crystal and WLS that mimics collagen helicity in crimp. Mater. Res. 4 (2001) 169-173
61. Vidal, B.C., Mello, M.L.S., 2009. Optical anisotropy of collagen fibers of rat calcaneal tendons: an approach to spatially resolved supramolecular organization. Acta Histochem. 111, doi:10.1016/j.acthis.2008.07.005.
62. Vidal B.C., and Vilarta R. Articular cartilage: collagen II-proteoglycan interactions. Availability of reactive groups. Variation in birefringence and differences as compared to collagen I. Acta Histochem. 83 (1988) 189-205
63. Vilarta R., and Vidal B.C. Anisotropic and biomechanical properties of tendons modified by exercise and denervation: aggregation and macromolecular order in collagen bundles. Matrix 9 (1989) 55-61
64. Whitesides G.M., Mathias J.P., and Seto C.T. Molecular self-assembly and nanochemistry: a chemical strategy for the synthesis of nanostructures. Science 254 (1991) 1312-1318
65. Whittaker P., Boughner D.R., Perkins D.G., and Canham P.B. Quantitative structural analysis of collagen in chordae tendineae and its relation to floppy mitral valves and proteoglycan infiltration. Br. Heart J. 57 (1987) 264-269
66. Williams R.M., Zipfel W.R., and Webb W.W. Interpreting second-harmonic generation images of collagen I fibrils. Biophys. J. 88 (2005) 1377-1386
67. Wilson E.E., Awonusi A., Morris M.D., Kohn D.H., Tecklenburg M.M., and Beck L.W. Highly ordered interstitial water observed in bone by nuclear magnetic resonance. J. Bone Miner. Res. 20 (2005) 625-634
68. Zubarev E.R., Pralle M.U., Li L.M., and Stupp S.I. Conversion of supramolecular clusters to macromolecular objects. Science 283 (1999) 523-526