Preservation of cartilage matrix proteoglycans using cationic dyes chemically related to ruthenium hexaammine trichlorideEB Hunziker, A Ludi and W Herrmann M. E. Muller Institute for Biomechanics, University of Bern, Switzerland. We tested various cationic dyes chemically related to ruthenium hexaammine trichloride (RHT) [i.e., the RHT-cyclohexanedione complex (RHT-CC), pentaamine ruthenium N-dimethylphenylenediimine trichloride (PRT), tris-(bipyridyl)ruthenium (II) chloride (TRC), tris (bipyridyl) iron (II) chloride (TIC), and cobalt hexaammine trichloride (CHT)] for their effectiveness in precipitating cartilage matrix proteoglycans in situ. Dyes were introduced into media at the onset of processing and were present throughout both aldehyde fixation and osmium tetroxide post-fixation. Contrary to expectation, most of the dye-proteoglycan complexes generated and stable under aldehyde fixation conditions were found to be unstable during post-fixation despite the continuing presence of the dye. A similar phenomenon was also found for the cationic dyes commonly used for precipitation of proteoglycans in cartilage tissue sections (such as Acridine Orange, Alcian Blue, Azure A, Methylene Blue, and Ruthenium Red). Only two dyes, i.e., RHT and the newly tested RHT-CC, formed proteoglycan precipitates sufficiently stable to resist disruption and extraction during osmium tetroxide post- fixation. The latter may be particularly useful in semiquantitative analyses of proteoglycan content in unstained tissue sections owing to its intense brown-black color. For applications in which the osmium tetroxide post-fixation step may be omitted, TRC and PRT may also be valuable for semiquantitative histochemistry by virtue of their stable fluorescence and intense violet color signals, respectively.
Volume 40,
Issue 7,
pp. 909-917,
07/01/1992
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P. Mainil-Varlet, T. Aigner, M. Brittberg, P. Bullough, A. Hollander, E. Hunziker, R. Kandel, S. Nehrer, K. Pritzker, S. Roberts, et al. Histological Assessment of Cartilage Repair: A Report by the Histology Endpoint Committee of the International Cartilage Repair Society (ICRS) J. Bone Joint Surg. Am., April 28, 2003; 85(90002): 45 - 57. [Full Text] |
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P. Saftig, E. Hunziker, O. Wehmeyer, S. Jones, A. Boyde, W. Rommerskirch, J. D. Moritz, P. Schu, and K. von Figura Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice PNAS, November 10, 1998; 95(23): 13453 - 13458. [Abstract] [Full Text] [PDF] |
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T. Quinn, A. Grodzinsky, M. Buschmann, Y. Kim, and E. Hunziker Mechanical compression alters proteoglycan deposition and matrix deformation around individual cells in cartilage explants J. Cell Sci., January 3, 1998; 111(5): 573 - 583. [Abstract] [PDF] |
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E. B. HUNZIKER and L. C. ROSENBERG Repair of Partial-Thickness Defects in Articular Cartilage: Cell Recruitment from the Synovial Membrane J. Bone Joint Surg. Am., May 1, 1996; 78(5): 721 - 33. [Abstract] [Full Text] |
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