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Vitreous collagen metabolism before and after vitrectomy

  • Clinical Investigation
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Abstract

Purpose

To assess vitreous metabolism by measuring C-propeptide levels of type II procollagen (pCOL-II-C) and hyaluronan levels in the vitreous and in the vitreous fluid after vitrectomy for macular hole.

Methods

We obtained 1-ml vitreous samples during vitrectomy from 34 patients (34 eyes) with a macular hole (age range 50–77 years, mean 64 years). After vitrectomy, we performed fluid–air exchange in six eyes because of unresolved macular holes and collected 4-ml fluid samples. Gel-filtration high-performance liquid chromatography (HPLC) was used to determine the molecular weight of pCOL-II-C in the samples. The pCOL-II-C level was measured by sandwich enzyme immunoassay and hyaluronan by sandwich binding protein assay.

Results

HPLC showed that pCOL-II-C in the vitreous samples corresponded to purified pCOL-II-C from cartilage. The vitreous pCOL-II-C level (4.7±0.3 ng/ml) was similar to reported synovial fluid levels. In six eyes that underwent fluid–air exchange, pCOL-II-C in the fluid samples remained at a level similar to that in the vitreous samples, while hyaluronan levels in the fluid samples were significantly lower than in the vitreous samples.

Conclusions

The molecular weight and concentrations of pCOL-II-C in the vitreous are similar to those in joint fluid. In patients with a macular hole, type II procollagen may be secreted persistently into the vitreous cavity before and after vitrectomy.

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References

  1. Atkinson EG, Jones S, Ellis BA, Dumonde DC, Graham E (1991) Molecular size of retinal vascular leakage determined by FITC–dextran angiography in patients with posterior uveitis. Eye 5:440–446

    PubMed  Google Scholar 

  2. Bishop PN, Reardon AJ, McLeod D, Ayad S (1994) Identification of alternatively spliced variants of type II procollagen in vitreous. Biochem Biophys Res Commun 203:289–295

    Article  PubMed  CAS  Google Scholar 

  3. Bishop PN, Reardon AJ, McLeod D, Ayad S (1994) Extraction and characterization of the tissue forms of collagen types II and IX from bovine vitreous. Biochem J 299:497–505

    PubMed  CAS  Google Scholar 

  4. Bishop PN (2000) Structural macromolecules and supramolecular organisation of the vitreous gel. Prog Retin Eye Res 19:323–344

    Article  PubMed  CAS  Google Scholar 

  5. Bishop PN, Takanosu M, Le Goff M, Mayne R (2002) The role of the posterior ciliary body in the biosynthesis of vitreous humour. Eye 16:454–460

    Article  PubMed  CAS  Google Scholar 

  6. Carey DE, Alini M, Ionescu M, Hyams JS, Rowe JC, Rosenberg LC, Poole AR (1997) Serum content of the C-propeptide of the cartilage molecule type II collagen in children. Clin Exp Rheumatol 15:325–328

    PubMed  CAS  Google Scholar 

  7. Chichibu K, Matsuura T, Shichijo S, Yokoyama M (1989) Assay of serum hyaluronic acid in clinical application. Clin Chim Acta 181:317–324

    Article  PubMed  CAS  Google Scholar 

  8. Choi HU, Tang LH, Johnson TL, Pal S, Rosenberg LC (1983) Isolation and characterization of 35,000 molecular weight subunit fetal cartilage matrix protein. J Biol Chem 258:655–661

    PubMed  CAS  Google Scholar 

  9. Ihanamaki T, Salminen H, Saamanen AM, Pelliniemi LJ, Hartmann DJ, Sandberg-Lall M, Vuorio E (2001) Age-dependent changes in the expression of matrix components in the mouse eye. Exp Eye Res 72:423–431

    Article  PubMed  CAS  Google Scholar 

  10. Larsson L, Osterlin S (1985) Posterior vitreous detachment: a combined clinical and physiochemical study. Graefes Arch Clin Exp Ophthalmol 223:92–95

    Article  PubMed  CAS  Google Scholar 

  11. Laurent TC, Fraser JR (1986) The properties and turnover of hyaluronan. Ciba Found Symp 124:9–29

    PubMed  CAS  Google Scholar 

  12. Los LI, van der Worp RJ, van Luyn MJ, Hooymans JM (2003) Age-related liquefaction of the human vitreous body: LM and TEM evaluation of the role of proteoglycans and collagen. Invest Ophthalmol Vis Sci 44:2828–2833

    Article  PubMed  Google Scholar 

  13. Nelson F, Dahlberg L, Laverty S, Reiner A, Pidoux I, Ionescu M, Fraser GL, Brooks E, Tanzer M, Rosenberg LC, Dieppe P, Robin Poole A (1998) Evidence for altered synthesis of type II collagen in patients with osteoarthritis. J Clin Invest 102:2115–2125

    Article  PubMed  CAS  Google Scholar 

  14. Newsome DA, Linsenmayer TF, Trelstad RL (1976) Vitreous collagen: evidence for a dual origin from the neural retina and hyalocytes. J Cell Biol 71:59–67

    Article  PubMed  CAS  Google Scholar 

  15. Peltonen L, Halila R, Ryhänen L (1985) Enzymes converting procollagens to collagens. J Cell Biochem 28:15–21

    Article  PubMed  CAS  Google Scholar 

  16. Reardon A, Sandell L, Jones CJ, McLeod D, Bishop PN (2000) Localization of pN-type IIA procollagen on adult bovine vitreous collagen fibrils. Matrix Biol 19:169–173

    Article  PubMed  CAS  Google Scholar 

  17. Rebuck N, Croucher LJ, Hollander AP (1999) Distribution of two alternatively spliced variants of the type II collagen N-propeptide compared with the C-propeptide in bovine chondrocyte pellet cultures. J Cell Biochem 75:13–21

    Article  PubMed  CAS  Google Scholar 

  18. Richards AJ, Morgan J, Bearcroft PW, Pickering E, Owen MJ, Holmans P, Williams N, Tysoe C, Pope FM, Snead MP, Hughes H (2002) Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule. J Med Genet 39:661–665

    Article  PubMed  CAS  Google Scholar 

  19. Savontaus M, Ihanamaki T, Metsaranta M, Vuorio E, Sandberg-Lall M (1997) Localization of type II collagen mRNA isoforms in the developing eyes of normal and transgenic mice with a mutation in type II collagen gene. Invest Ophthalmol Vis Sci 38:930–942

    PubMed  CAS  Google Scholar 

  20. Shinmei M, Ito K, Matsuyama S, Yoshihara Y, Matsuzawa K (1993) Joint fluid carboxy-terminal type II procollagen peptide as a marker of cartilage collagen biosynthesis. Osteoarthr Cartil 1:121–128

    Article  PubMed  CAS  Google Scholar 

  21. Sugiyama S, Itokazu M, Suzuki Y, Shimizu K (2003) Procollagen II C propeptide level in the synovial fluid as a predictor of radiographic progression in early knee osteoarthritis. Ann Rheum Dis 62:27–32

    Article  PubMed  CAS  Google Scholar 

  22. Takanosu M, Boyd TC, Le Goff M, Henry SP, Zhang Y, Bishop PN, Mayne R (2001) Structure, chromosomal location, and tissue-specific expression of the mouse opticin gene. Invest Ophthalmol Vis Sci 42:2202–2210

    PubMed  CAS  Google Scholar 

  23. Uitto J, Allan RE, Polak KL (1979) Conversion of type II procollagen to collagen. Eur J Biochem 99:97–103

    Article  PubMed  CAS  Google Scholar 

  24. Van Der Rest M, Rosenberg LC, Olsen BR, Poole AR (1986) Chondrocalcin is identical with the C-propeptide of type II procollagen. Biochem J 237:923–925

    PubMed  Google Scholar 

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Acknowledgement

Supported in part by a grant-in-aid for scientific research from the Ministry of Education, Science, Sport and Culture of Japan (SK).

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Correspondence to Shoji Kishi.

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Itakura, H., Kishi, S., Kotajima, N. et al. Vitreous collagen metabolism before and after vitrectomy. Graefe's Arch Clin Exp Ophthalmo 243, 994–998 (2005). https://doi.org/10.1007/s00417-005-1150-9

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  • DOI: https://doi.org/10.1007/s00417-005-1150-9

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