Expression of keratin K2e in cutaneous and oral lesions: association with keratinocyte activation, proliferation, and keratinization.

Balvinder K Bloor, Nicholas Tidman, Irene M Leigh, Edward Odell, Bilal Dogan, Uwe Wollina, Lucy Ghali, Ahmad Waseem
Author Information
  1. Balvinder K Bloor: Head and Neck Cancer Research Program, Guy's, King's, and St. Thomas's Dental Institute, King's College London, London, United Kingdom.

Abstract

The cytoskeleton in keratinocytes is a complex of highly homologous structural proteins derived from two families of type I and type II polypeptides. Keratin K2e is a type II polypeptide that is expressed in epidermis late in differentiation. Here we report the influence of keratinocyte activation, proliferation, and keratinization on K2e expression in samples of cutaneous and oral lesions. The normal expression of K2e in the upper spinous and granular layers of interfollicular epidermis is increased in keloid scars but showed distinct down-regulation in psoriasis and hypertrophic scars where keratinocytes are known to undergo activation. Unlike normal and psoriatic skin, K2e expression in hypertrophic and keloid scars began in the deepest suprabasal layer. In cutaneous basal and squamous cell carcinomas, K2e was absent in most tumor islands but the overlying epidermis showed strong expression. No significant K2e expression in nonkeratinized or keratinized oral epithelia, including buccal mucosa, lateral border of tongue and gingiva was detected. In oral lichen planus K2e expression was undetectable, but in benign keratoses of lingual mucosa induction of K2e along with K1 and K10 was observed. In mild-to-moderate oral dysplasia with orthokeratinization, K2e was highly expressed compared with parakeratinized areas but in severe dysplasia as well as in oral squamous cell carcinoma, K2e expression was undetectable. Taken together, the data suggest that K2e expression in skin is sensitive to keratinocyte activation but its up-regulation in oral lesions is a reflection of the degree of orthokeratinization.

References

  1. J Cell Biol. 1984 Apr;98(4):1397-406 [PMID: 6201492]
  2. Br J Dermatol. 1993 Aug;129(2):110-9 [PMID: 7544603]
  3. Ann N Y Acad Sci. 1985;455:307-29 [PMID: 2417518]
  4. Ann N Y Acad Sci. 1985;455:614-34 [PMID: 3002221]
  5. Differentiation. 1987;33(3):254-65 [PMID: 2439403]
  6. Differentiation. 1987;34(3):189-200 [PMID: 2448177]
  7. Ups J Med Sci. 1987;92(3):253-7 [PMID: 2452504]
  8. J Cell Biol. 1989 Jul;109(1):295-307 [PMID: 2473080]
  9. Br J Dermatol. 1995 Oct;133(4):501-11 [PMID: 7577575]
  10. Br J Dermatol. 1995 Dec;133(6):830-5 [PMID: 8547031]
  11. Exp Cell Res. 1996 Mar 15;223(2):203-14 [PMID: 8601396]
  12. Annu Rev Cell Dev Biol. 1995;11:123-53 [PMID: 8689554]
  13. Science. 1997 Apr 4;276(5309):75-81 [PMID: 9082989]
  14. Physiol Rev. 1997 Apr;77(2):397-424 [PMID: 9114819]
  15. Biochem Biophys Res Commun. 1997 Jul 18;236(2):231-8 [PMID: 9240415]
  16. Mol Carcinog. 1997 Sep;20(1):3-9 [PMID: 9328431]
  17. Int J Biochem Cell Biol. 1997 Jul;29(7):971-83 [PMID: 9375377]
  18. Am J Pathol. 1998 May;152(5):1133-41 [PMID: 9588880]
  19. Lab Invest. 1998 Jul;78(7):787-95 [PMID: 9690557]
  20. J Invest Dermatol. 1998 Nov;111(5):762-6 [PMID: 9804335]
  21. J Invest Dermatol. 1998 Nov;111(5):817-21 [PMID: 9804344]
  22. J Invest Dermatol. 1999 Mar;112(3):362-9 [PMID: 10084315]
  23. Br J Dermatol. 1999 Apr;140(4):582-91 [PMID: 10233306]
  24. J Invest Dermatol. 1999 Aug;113(2):246-50 [PMID: 10469311]
  25. Plast Reconstr Surg. 1999 Oct;104(5):1435-58 [PMID: 10513931]
  26. J Cell Sci. 1990 May;96 ( Pt 1):121-9 [PMID: 1695635]
  27. J Invest Dermatol. 2000 Mar;114(3):487-93 [PMID: 10692107]
  28. J Oral Pathol Med. 2000 Sep;29(8):376-84 [PMID: 10972346]
  29. Cytobios. 2001;104(405):43-51 [PMID: 11219730]
  30. Oral Oncol. 2001 Apr;37(3):251-61 [PMID: 11287279]
  31. J Invest Dermatol. 2001 May;116(5):633-40 [PMID: 11348449]
  32. J Pathol. 2001 Jun;194(2):207-16 [PMID: 11400150]
  33. J Am Acad Dermatol. 2002 Feb;46(2):207-14 [PMID: 11807431]
  34. J Biol Chem. 2002 May 24;277(21):19122-30 [PMID: 11889133]
  35. J Biol Chem. 2002 Sep 20;277(38):35371-7 [PMID: 12119299]
  36. Cell. 1982 Nov;31(1):11-24 [PMID: 6186379]
  37. Cell. 1990 Oct 19;63(2):425-35 [PMID: 2145076]
  38. J Cell Sci. 1990 Sep;97 ( Pt 1):39-50 [PMID: 1701769]
  39. New Biol. 1990 May;2(5):464-78 [PMID: 1705144]
  40. Am J Pathol. 1991 Mar;138(3):751-63 [PMID: 1705754]
  41. J Invest Dermatol. 1991 Apr;96(4):414-8 [PMID: 2007780]
  42. Differentiation. 1990 Dec;45(3):221-9 [PMID: 2090523]
  43. J Invest Dermatol. 1991 Nov;97(5):763-70 [PMID: 1717607]
  44. J Biol Buccale. 1991 Sep;19(3):187-98 [PMID: 1718955]
  45. J Invest Dermatol. 1992 Feb;98(2):154-61 [PMID: 1370674]
  46. Br J Dermatol. 1992 Feb;126(2):154-60 [PMID: 1371396]
  47. J Invest Dermatol. 1992 Mar;98(3):343-50 [PMID: 1372028]
  48. Exp Cell Res. 1992 Sep;202(1):132-41 [PMID: 1380918]
  49. J Invest Dermatol. 1992 Sep;99(3):283-8 [PMID: 1355099]
  50. Differentiation. 1992 Oct;51(2):137-48 [PMID: 1282112]
  51. J Dermatol. 1992 Nov;19(11):781-5 [PMID: 1284071]
  52. J Cell Biochem Suppl. 1993;17F:167-74 [PMID: 8412188]
  53. J Cell Sci. 1993 Sep;106 ( Pt 1):175-82 [PMID: 7505781]
  54. Differentiation. 1993 Dec;55(1):57-71 [PMID: 7507869]
  55. J Invest Dermatol. 1994 Feb;102(2):165-70 [PMID: 7508961]
  56. J Invest Dermatol. 1994 Sep;103(3):277-81 [PMID: 7521371]
  57. Eur J Cancer B Oral Oncol. 1994 May;30B(3):160-6 [PMID: 7522710]
  58. Nat Genet. 1994 Aug;7(4):485-90 [PMID: 7524919]
  59. Annu Rev Biochem. 1994;63:345-82 [PMID: 7979242]
  60. J Cell Biol. 1995 Mar;128(6):1209-19 [PMID: 7534766]
  61. J Cell Biol. 1995 Jun;129(5):1329-44 [PMID: 7539810]
  62. Ann N Y Acad Sci. 1985;455:282-306 [PMID: 2417517]

MeSH Term

Animals
Antibodies, Monoclonal
Base Sequence
Breast
Cell Division
DNA Primers
Epidermal Cells
Epidermis
Female
Gene Expression Regulation
Genetic Variation
Gingiva
Humans
In Situ Hybridization
Keloid
Keratinocytes
Keratins
Mice
Mouth Mucosa
Peptide Fragments
Polymerase Chain Reaction
Protein Isoforms
Psoriasis
Skin

Chemicals

Antibodies, Monoclonal
DNA Primers
Peptide Fragments
Protein Isoforms
Keratins

Word Cloud

Created with Highcharts 10.0.0K2eexpressionoralactivationtypeepidermiskeratinocytecutaneousscarskeratinocyteshighlyIIexpressedproliferationkeratinizationlesionsnormalkeloidshowedhypertrophicskinsquamouscellmucosaundetectabledysplasiaorthokeratinizationcytoskeletoncomplexhomologousstructuralproteinsderivedtwofamiliespolypeptidesKeratinpolypeptidelatedifferentiationreportinfluencesamplesupperspinousgranularlayersinterfollicularincreaseddistinctdown-regulationpsoriasisknownundergoUnlikepsoriaticbegandeepestsuprabasallayerbasalcarcinomasabsenttumorislandsoverlyingstrongsignificantnonkeratinizedkeratinizedepitheliaincludingbuccallateralbordertonguegingivadetectedlichenplanusbenignkeratoseslingualinductionalongK1K10observedmild-to-moderatecomparedparakeratinizedareasseverewellcarcinomaTakentogetherdatasuggestsensitiveup-regulationreflectiondegreeExpressionkeratinlesions:association

Similar Articles

Cited By