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Tenascin in inflammatory conditions and neoplasms of the urinary bladder

  • Published:
Virchows Archiv B

Summary

Tenascin (Tn) is an extracellular matrix (ECM) glycoprotein strongly and widely expressed during embryogenesis. Tn is decreased in normal adult tissues but is reexpressed in numerous inflammatory, reparative and neoplastic processes. We immunostained samples of fetal and normal adult bladders and samples of bladder tissue from patients with chronic cystitis, detrusor hypertrophy, malakoplakia and transitional cell carcinomas (TCC) of all grades, with a monoclonal antibody (mAb) to Tn 143DB7. Sections of flat in situ carcinomas were also studied. In fetal bladders, strong and ragged Tn reactions were noted at the epithelial-stromal interface; in normal adult bladders, the reaction was delicate and less extensive. In chronic cystitis, Tn reactivity was enhanced particularly around prominent capillary blood vessels. In flat in situ carcinomas, Tn staining was stronger and more extensive than in normal mucosa but was often less extensive than in some examples of cystitis. In TCC I and II, Tn immunoreactivity was strong and predominated in the pericapillary stroma of the papillae; in infiltrating TCC II, comparatively limited Tn staining was noted. In deeply infiltrating grade III TCC with abundant stroma, Tn reaction was invariably strong and extensive, particularly around advancing tumor nests. The strongest Tn reactions were noted in invasive, high-grade TCC with abundant stroma. We conclude that in inflammatory-reactive processes, and in in situ carcinomas as well as in TCC, the extent and intensity of the Tn reaction correlates with the severity of the inflammatory infiltrate and with the extent of the stromal remodelling.

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References

  • Aufderheide E, Ekblom P (1988) Tenascin during gut development: appearance in the mesenchyme, shift in molecular forms, and dependance on epithelial-mesenchymal interactions. J Cell Biol 107:2341–2349

    Article  PubMed  CAS  Google Scholar 

  • Aufderheide E, Chiquet-Ehrishmann R, Ekblom P (1987) Epitheli-al-mesenchymal interactions in the developing kidney lead to expression of tenascin in the mesenchyme. J Cell Biol 105:599–608

    Article  PubMed  CAS  Google Scholar 

  • Chiquet-Ehrismann R (1990) What distinguishes tenascin from fibronectin. FASEB J 4:2598–2604

    PubMed  CAS  Google Scholar 

  • Chiquet M, Fambrough DM (1984) Chick myotenchinous antigen. I. A monoclonal antibody as marker for tendon and muscle morphogenesis. J Cell Biol 98:1926–1936

    Article  PubMed  CAS  Google Scholar 

  • Chiquet-Ehrismann R, Mackie EJ, Pearson CA, Sakakura T (1986) Tenascin: an extracellular matrix protein involved in tissue interactions during fetal development and oncogenesis. Cell 47:131–139

    Article  PubMed  CAS  Google Scholar 

  • Chiquet-Ehrismann R, Kalla P, Pearson CA (1989) Participation of tenascin and transforming growth factor-β in resiprocal epithelial-mesenchymal interactions of MCF7 cells and fibroblasts. Cancer Res 49:4322–4325

    PubMed  CAS  Google Scholar 

  • Chuong CM, Chen HM (1991) Enhanced expression of neural cell adhesion molecules and tenascin (cytotactin) during wound healing. Am J Pathol 138:427–440

    PubMed  CAS  Google Scholar 

  • Crossin KL, Hoffman S, Grumet M, Thiery JP, Edelman G (1986) Site-restricted expression of cytotactin during development of the chicken embryo. J Cell Biol 102:1917–1930

    Article  PubMed  CAS  Google Scholar 

  • Dvorak HF (1986) Tumors: wounds that do not heal. N Engl J Med 25:1650–1655

    Google Scholar 

  • Ekblom P, Aufderheide E (1989) Stimulation of tenascin expression in mesenchyme by epithelial-mesenchymal interactions. Int J Dev Biol 33:71–79

    PubMed  CAS  Google Scholar 

  • Erickson HP, Bourdon MA (1989) Tenascin: an extracellular matrix protein prominent in specialized embryonic tissues and tumors. Annu Rev Cell Biol 5:71–92

    Article  PubMed  CAS  Google Scholar 

  • Eyken P van, Gearts A, Bleser P de, Jazon JM, Vrijsen R, Sciot R, Wisse E, Desmet VJ (1992) Localization and cellular source of the extracellular matrix protein tenascin in normal and fibrotic rat liver. Hepatology 15:909–916

    Article  PubMed  Google Scholar 

  • Gould VE, Koukoulis K, Virtanen I (1990) Extracellular matrix proteins and their receptors in the normal, hyperplastic and neoplastic breast. Cell Differ Dev 32:409–416

    Article  PubMed  CAS  Google Scholar 

  • Gould VE, Martinez-Lacabe V, Virtanen I, Sahlin KM, Schwartz MM (1992) Differential distribution of tenascin and cellular fibronectins in acute and chronic renal allograft rejection. Lab Invest 67:71–79

    PubMed  CAS  Google Scholar 

  • Howeedy AA, Virtanen I, Laitinen L, Gould NS, Koukoulis GK, Gould VE (1990) Differential distribution of tenascin in the normal, hyperplastic, and neoplastic breast. Lab Invest 63:798–806

    PubMed  CAS  Google Scholar 

  • Hsu SM, Raine L, Fanger H (1981) The use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures. J Histochem Cytochem 29:553–560

    Google Scholar 

  • Jones FJ, Burgoon MP, Hoffman S, Crossin KL, Cunningham BA, Edelman GM (1988) A cDNA clone for cytotactin contains sequences similar to epidermal growth factor-like repeats and segments of fibronectin and fibrinogen. Proc Natl Acad Sci USA 85:2186–2190

    Article  PubMed  CAS  Google Scholar 

  • Koch M, Wehrle-Haller B, Baumgartner S, Spring J, Brubacher D, Chiquet M (1991) Epithelial synthesis of tenascin at tips of growing bronchi and graded accumulation in basement membrane and mesenchyme. Exp Cell Res 194:297–300

    Article  PubMed  CAS  Google Scholar 

  • Koss LG (1975) Tumors of the urinary bladder. Atlas of tumor pathology. Armed Forces Institute of Pathology, Washington, DC

    Google Scholar 

  • Koukoulis GK, Gould VE, Bhattacharyya A, Gould JE, Howeedy AA, Virtanen I (1991) Tenascin in normal, reactive, hyperplastic, and neoplastic tissues: biologic and pathologic implications. Hum Pathol 22:636–643

    Article  PubMed  CAS  Google Scholar 

  • Luomanen M, Virtanen I (1992) Distribution of tenascin in healing incision, excision and laser wounds. J Oral Pathol Med (in press)

  • Mackie EJ, Thesleff I, Chiquet-Ehrismann R (1987a) Tenascin is associated with chondrogenic and osteogenic differentiation in vivo and promotes chondrogenesis in vitro. J Cell Biol 105:2569–2579

    Article  PubMed  CAS  Google Scholar 

  • Mackie EJ, Chiquet-Ehrismann R, Pearson CA, Inaguma Y, Taya K, Kawarada Y, Sakakura T (1987 b) Tenascin is a stromal marker for epithelial malignancy in the mammary gland. Proc Natl Acad Sci USA 84:4621–4625

    Article  PubMed  CAS  Google Scholar 

  • Mackie EJ, Halfter W, Liverani D (1988) Induction of tenascin in healing wounds. J Cell Biol 107:2757–2767

    Article  PubMed  CAS  Google Scholar 

  • Natali PG, Nicotra MR, Bigotti A, Botti C, Castellani P, Risso AM, Zardi L (1991) Comparative analysis of the expression of the extracellular matrix protein tenascin in normal human fetal, adult and tumor tissues. Int J Cancer 47:811–816

    Article  PubMed  CAS  Google Scholar 

  • Pearson CA, Pearson D, Shibahara S, Hofsteenge J, Chiquet-Ehrismann R (1988) Tenascin: cDNA cloning and induction by TGF-β. EMBO J 7:2977–2981

    PubMed  CAS  Google Scholar 

  • Prieto AL, Jones FS, Cunningham BA, Crossin KL, Edelman GM (1990) Localization during development of alternatively spliced forms of cytotactin mRNA by in situ hybridization. J Cell Biol 111:685–698

    Article  PubMed  CAS  Google Scholar 

  • Siri A, Carnemolla B, Saginati M, Leprini A, Casari G, Baralle F, Zardi L (1991) Human tenascin: primary structure, pre-mRNA splicing patterns and localization of the epitopes recoqnized by to monoclonal antibodies. Nucleic Acids Res 19:525–531

    Article  PubMed  CAS  Google Scholar 

  • Tervo K, Tervo T, Setten GB van, Tarkkanen A, Virtanen I (1989) Demonstration of tenascin-like immunoreactivity in rabbit corneal wounds. Acta Ophtalmol 67:347–350

    Article  CAS  Google Scholar 

  • Thesleff I, Mackie E, Vainio S, Chiquet-Ehrismann R (1987) Changes in the distribution of tenascin during tooth development. Development 101: 289–296

    PubMed  CAS  Google Scholar 

  • Tiitta O, Wahlström T, Paavonen J, Linnala A, Sharma S, Gould VE, Virtanen I (1992) Enhanced tenascin expression in cervical and vulvar koilocytotic lesions. Am J Pathol 141:907–915

    PubMed  CAS  Google Scholar 

  • Vollmer G, Siegal GP, Chiquet-Ehrismann R, Lightner VA, Arhholdt H, Knuppen R (1990) Tenascin expression in the human endometrium and in endometrial adenocarcinomas. Lab Invest 62:725–730

    PubMed  CAS  Google Scholar 

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Tiitta, O., Wahlström, T., Virtanen, I. et al. Tenascin in inflammatory conditions and neoplasms of the urinary bladder. Virchows Archiv B Cell Pathol 63, 283–287 (1993). https://doi.org/10.1007/BF02899274

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