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Immunomodulating properties and tissue distribution of aromatic retinoids in the immunologically responsive albino rabbit eye

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Abstract

The effects of retinoid Ro 10-9359 on normal albino rabbit eyes and antigen-induced intra-ocular inflammations were investigated. The distribution pattern of intravenously applied 3H — Ro 10-9359 correlated well with the sites of pharmacological action. Whereas immunologically naive rabbits showed a uveal uptake of 0.164 ng/g wet wt. tissue when 100 μg of Ro 10-9359 was administered intravenously, accumulation may amount up to 17.46 ng/g in secondary ocular immune responses. Ro 10-9359 accumulated markedly during secondary stimulation in the uvea, preauricular lymph nodes and the spleen. The chemotactic peptide NForm-Leu-Leu-Phe used to incite a hypopyon attracted Ro 10-9359 into the anterior chamber in vivo.

This study indicates that the aromatic retinoid Ro 10-9359 is able to alter certain immune responses and may be involved in intercellular communication during secondary immune responses in the albino rabbit eye.

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References

  • Barnett ML, Szabo G (1973) Effect of vitamin A on epithelial morphogenesis in vitro. Exp Cell Res 76:118–126

    Google Scholar 

  • Bauer R, Orfanos CE (1981) Influence of retinoid on human blood cells in vitro. TMMP-retinoid inhibits the mitogenic properties of lectins and modulates the lymphocytic response. In: Orfanos CE (ed) Retinoids. Springer-Verlag, Berlin Heidelberg New York pp 153–160

    Google Scholar 

  • Berretti B, Grupper C, Edelson Y, Bermejo D (1981) Aromatic retinoids in the treatment of multiple superficial basal cell carcinoma, arsenic keratosis and keratoacanthoma. In: Orfanos CE (ed) Retinoids. Springer-Verlag, Berlin Heidelberg New York pp. 397–399

    Google Scholar 

  • Bialasiewicz AA, Lubach D, Marghescu S (1981a) Immunological features of psoriasis. Arch Derm Res 271:29–40

    Google Scholar 

  • Bialasiewicz AA, Lubach D, Marghescu S (1981b) Effects of Ro 10–9359 conconavalin A pokeweed mitogen and methotrexate on cultivated lymphocytes. In: Orfanos CE (ed) Retinoids. Springer-Verlag, Berlin Heidelberg New York, pp 335–338

    Google Scholar 

  • Blalock JE, Gifford GE (1977) Retinoic acid induced transcriptional control of interferon production. Proc Natl Acad Sci USA 74:5382–5385

    Google Scholar 

  • Cohen BE, Cohen IK (1973) Vitamin A: adjuvant and steroid antagonist in the immune response. J Immunol 111:1376–1380

    Google Scholar 

  • DeLuca LM, Yuspa SH (1974) Altered glycoprotein synthesis in mouse epidermal cells treated with retinyl acetate in vitro. Exp Cell Res 86:106–111

    Google Scholar 

  • Dennert G, Lotan R (1978) Effects of retinoic acid on the immune system: Stimulation of T-killer cell induction. Eur J Immunol 8:23–29

    Google Scholar 

  • Dresser DN (1968) Adjuvanticity of vitamin A. Nature (London) 217:527–529

    Google Scholar 

  • Goodman DWS (1981) Vitamin A transport and delivery and the mechanism of vitamin A toxicity. In: Orfanos CE (ed) Retinoids. Springer-Verlag, Berlin Heidelberg New York, pp 31–40

    Google Scholar 

  • Harris LS, Toyofoku H, Shimmyo M (1972) Fluorescein iris angiography in the albino rabbit. Arch Ophthalmol 88:193–195

    Google Scholar 

  • Hercend T, Bruley-Rosset M, Florentin I, Mathé (1981) In vivo immunostimulating properties of two retinoids. In: Orfanos CE (ed) Retinoids. Springer-Verlag, Berlin Heidelberg New York, pp 21–30

    Google Scholar 

  • Hook WA, Schiffmann E, Aswanikumar S, Siragowian R (1976) Histamine release by chemotactic formyl methionine containing peptides. J Immunol 117/2:594–596

    Google Scholar 

  • Jetten AM, Jetten MER, Shapiro SS, Poon JP (1979) Characterization of the action of retinoids on mouse fibroblast cell lines. Exp Cell Res 119:289–299

    Google Scholar 

  • Jurin M, Tannok IF (1972) Influence of vitamin A on immunological responses. Immunology 23:283–287

    Google Scholar 

  • King IA, Tabiowo A (1981) The effect of all-trans retinoic acid on the synthesis of epidermal cell surface associated carbohydrates. Biochem J 194:341–350

    Google Scholar 

  • Levine L, Ohuchi K (1978) Retinoids as well as tumor promoters enhance deacylation of cellular lipids and prostaglandin production in MDCK cells. Nature (London) 276:274–275

    Google Scholar 

  • Orfanos CE (1980) Oral retinoids — present status. Br J Dermatol 103:473–481

    Google Scholar 

  • Orfanos CE, Landes E, Bloch PH (1978) Traitement du psoriasis pustuleux par une nouveaux rétinoide aromatique. Ann Dermatol Venereol 105:807–811

    Google Scholar 

  • Paravicini U (1981) Pharmokokinetics and metabolism of oral aromatic retinoids. In: Orfanos CE (ed) Retinoids. Springer-Verlag. Berlin Heidelberg New York pp 13–20

    Google Scholar 

  • Patt LM, Heya K, Hakamori S (1978) Retinal induces density — dependent growth inhibition and changes in glycolipids and LETS. Nature (London) 273:379–381

    Google Scholar 

  • Rando RR, Bangerter FW (1982) The rapid intermembraneous transfer of retinoids. Biophys Biochem Res Comm 104/2:430–436

    Google Scholar 

  • Schroder EW, Black PA (1980) Retinoids: tumor promoters or tumor enhancers? J Natl Cancer Inst 65:671–674

    Google Scholar 

  • Shapiro SS, Poon JP (1979) Retinoic acid induced alterations of growth and morphology in an established epithelial cell line. Exp Cell Res 119:349–357

    Google Scholar 

  • Snyderman R (1981) Chemotactic receptors on leucocytes. In: Suran E, Gery I, Nussenblatt RB (eds) Immunology of the eye, III. IRL Press, Washington, pp 309–323

    Google Scholar 

  • Sporn MB (1981) Retinoids: new developments in their mechanism of action as related to control of proliferative diseases. In: Orfanos CE (ed) Retinoids. Springer-Verlag, Berlin Heidelberg New York, pp 73–76

    Google Scholar 

  • Todaro GJ, DeLarco JE, Sporn MB (1978) Retinoids block phenotypic cell transformation produced by sarcoma growth factor. Nature (London) 276:272–274

    Google Scholar 

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Bialasiewicz, A.A., Kopp, U., Mahlstedt, J. et al. Immunomodulating properties and tissue distribution of aromatic retinoids in the immunologically responsive albino rabbit eye. Graefe's Arch Clin Exp Ophthalmol 220, 268–272 (1983). https://doi.org/10.1007/BF00231354

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  • DOI: https://doi.org/10.1007/BF00231354

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