Skip to main content
Log in

Alpha-smooth muscle actin and other stromal markers in endometrial mucosa

  • Original Articles
  • Published:
Virchows Archiv A Aims and scope Submit manuscript

Abstract

Stromal-epithelial interactions as expressed by alpha-smooth muscle actin (alpha-SM actin) collagen type IV, fibronectin, laminin and tenascin were studied in normal and pathological endometrial mucosa. There was complete or incomplete cuffing of scattered endometrial glands by alpha-SM actin mostly in the basal layer of endometrial mucosa and in dilated or cystic glands. Individual adenocarcinomatous glands were not encircled by alpha-SM actin-positive cells. Collagen type IV and laminin were found surrounding all glands irrespective of the presence of periglandular alpha-SM actin. Fibronectin was diffusely present in the stroma. Tenascin was identified, albeit not exclusively, in a periglandular location similar to that of alpha-SM actin. We conclude that the periglandular cells staining for alpha-SM actin, which were negative for cytokeratins, are probably myofibroblasts (MFs). Since this phenomenon was most commonly observed in dilated and cystic glands, we suggest that stromal cells immediately surrounding these glands may be subjected to mechanical or other stress resulting, as in other situations of tissue remodelling, in the development of MFs. This may also explain the appearance of tenascin in the same location. Thus, our finding may represent a further example of the local modulation of stromal cell phenotype, possibly under the action of micro-environmental factors.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Aggarwal BB, Pocsik E (1992) Cytokines: from clone to clinic. Arch Biochem 292:335–359

    Google Scholar 

  • Barcellos-Hoff MH, Aggeler J, Ram TG, Bissei MJ (1989) Functional differentiation and alveolar morphogenesis of primary mammary basement membrane. Development 105:223–235

    Google Scholar 

  • Bo WJ, Odor DL, Rockvock MF (1968) Ultrastructure of uterine smooth muscle following progesterone or progesterone-estrogen treatment. Anat Rec 163:121–132

    Google Scholar 

  • Bussolati GC (1980) Actin-rich (myoepithelial) cells in lobular carcinoma in situ of the breast. Virchows Arch [B] 32:165–176

    Google Scholar 

  • Cintorino M, Bellizzi de Marco E, Leoncini P, Tripodi SA, Ramaekers F, Sappino AP, Schmitt-Gräff A, Gabbiani G (1991) Expression of alpha-smooth muscle actin in stromal cells of the uterine cervix during epithelial neoplastic changes. Int J Cancer 47:843–846

    Google Scholar 

  • Czernobilsky B, Shezen E, Lifschitz-Mercer B, Fogel M, Luzon A, Jacob N, Skalli O, Gabbiani G (1989) Alpha-smooth muscle actin (alpha-SM actin) in normal human ovaries, in ovarian stromal hyperplasia and in ovarian neoplasms. Virchows Arch [B] 57:55–61

    Google Scholar 

  • Desmoulière A, Rubbia-Brandt L, Abdiu A, Walz T, Macieira-Coelho A, Gabbiani G (1992)α-smooth muscle actin is expressed in a subpopulation of cultured and cloned fibroblasts and is modulated byγ-interferon. Exp Cell Res 201:64–73

    Google Scholar 

  • Desmoulière A, Rubbia-Brandt L, Grau G, Gabbiani G (1992) Heparin inducedα-smooth muscle actin expression in cultured fibroblasts and in granulation tissue myofibroblasts. Lab Invest 67:716–726

    Google Scholar 

  • Donjacour AD, Cunha GR (1991) Stromal regulation of epithelial function. In: Lipmann M, Dickson R (eds) Regulatory mechanisms in breast cancer. Kluwer Academic, Boston, pp 335–364

    Google Scholar 

  • Franke WW, Appelhans B, Schmid E, Freudenstein C, Osborn M, Weber K (1979) Identification and characterization of epithelial cells in mammalian tissues by immunofluorescence microscopy using antibodies to prekeratin. Differentiation 15:7–25

    Google Scholar 

  • Gabbiani G, Ryan GB, Majno G (1971) Presence of modified fibroblasts in granulation tissue and their possible role in wound contraction. Experientia 27:549–550

    Google Scholar 

  • Haffen K, Kedinger M, Simon-Assmann P (1987) Mesenchyme-dependent differentiation of epithelial progenitor cells in the gut. J Pediatr Gastroenterol Nutr 6:14–23

    Google Scholar 

  • Hodges GM (1982) Tumor formation: the concept of tissue (stromal-epithelium) regulatory dysfunction. In: Pitts JD, Finbow ME (eds) The functional integration of cells in animal tissues. Cambridge University Press, Cambridge, pp 333–356

    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

    Google Scholar 

  • Hsu SM, Raine L, Fanger H (1981) Use of avidin-biotin peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabelled antibody (PAP) procedure. J Histochem Cytochem 29:577–580

    Google Scholar 

  • Kawaguchi K, Fujii S, Konishi I, Okamura H, Mori T (1985) Ultrastructural study of cultured smooth muscle cells from uterine leiomyoma and myometrium under the influence of sex steroids. Gynecol Oncol 21:32–41

    Google Scholar 

  • Kocher O, Skalli O, Bloom WS, Gabbiani G (1984) Cytoskeleton of rat aortic smooth muscle cells: Normal conditions and experimental intimai thickening. Lab Invest 50:645–652

    Google Scholar 

  • Kratochwil K (1986) The stroma and the control of cell growth. J Pathol 149:23–24

    Google Scholar 

  • Liotta LA, Roa CN, Werwer UM (1986) Biochemical interactions of tumor cells with the basement membrane. Annu Rev Biochem 55:1037–1057

    Google Scholar 

  • Liotta LA, Steeg PS, Stettier-Stevenson G (1991) Cancer metastasis and angiogenesis: an imbalance of positive and negative regulation. Cell 64:327–336

    Google Scholar 

  • Mackie EJ, Halfter W, Liverani D (1988) Induction of tenascin in healing wounds. J Cell Biol 107:2257–2767

    Google Scholar 

  • Montesano R, Schaller G, Orci L (1991) Induction of epithelial tubular morphogenesis in vitro by fibroblast-derived soluble factors. Cell 66:697–711

    Google Scholar 

  • Nagle RB, Böcker W, Davin JR, Heid HW, Kaufmann U, Lucas DO, Jarasch ED (1986) Characterization of breast carcinomas by two nomoclonal antibodies distinguishing myoepithelial from luminal epithelial cells. J Histochem Cytochem 34:869–881

    Google Scholar 

  • Nakanishi Y, Ishii T (1989) Epithelial shape change in mouse embryonic submandibular gland: modulation by extracellular matrix components. Bioessays 11:163–167

    Google Scholar 

  • Nathrath WBJ, Wilson PD, Trejdosiewicz LK (1982) Immunohistochemical localization of keratin and luminal epithelial antigen in myoepithelial and luminal epithelial cells of human mammary and salivary gland tumors. Pathol Res Pract 175:279–288

    Google Scholar 

  • Ross R, Klebanoff SJ (1967) Fine structural changes in uterine smooth muscle and fibroblasts in response to estrogen. J Cell Biol 32:155–169

    Google Scholar 

  • Ruoslahti E (1989) Proteoglycans in cell regulation. J Biol Chem 264:13369–13372

    Google Scholar 

  • Sappino AP, Skalli O, Jackson B, Schürch W, Gabbiani G (1988) Smooth-muscle differentiation in stromal cells of malignant and non-malignant breast tissues. Int J Cancer 41:707–712

    Google Scholar 

  • Sappino AP, Dietrich PY, Skalli O, Widgren S, Gabbiani GH (1989) Colonic pericryptal fibroblasts. Differentiation pattern in embryogenesis and phenotypic modulation in epithelial proliferative lesions. Virchows Arch [A] 415:551–557

    Google Scholar 

  • Sappino AP, Schürch W, Gabbiani G (1990) Differentiation repertoire of fibroblastic cells: expression of cytoskeletal proteins as marker of phenotypic modulations. Lab Invest 63:144–161

    Google Scholar 

  • Schmitt-Gräff A, Gabbiani G (1992) Phenotypic features of stromal cells in normal, premalignant and malignant conditions. Eur J Cancer 28A: 1916–1920

    Google Scholar 

  • Schürch W, Seemayer TA, Gabbiani G (1992) Myofibroblasts. In: Sternberg SS (ed): Histology for pathologists. Raven Press, New York, pp 109–144

    Google Scholar 

  • Schalkwijk J, Skejlen PM, Vlimmen-Willems IMJJ van, Oosterling B, Mackie EJ, Verstraeten AA (1991) Tenascin expression in human dermis related to epidermal proliferation. Am J Pathol 139:1143–1150

    Google Scholar 

  • Seemayer TA, Lagacé R, Schürch W, Tremblay G (1979) Myofibroblasts in the stroma of invasive and metastatic carcinoma: a possible host response to neoplasia. Am J Surg Pathol 3:525–533

    Google Scholar 

  • Skalli O, Gabbiani G (1988) The biology of the myofibroblast. Relationship to wound contraction and fibrocontractive disease. In: Clark RAF, Henson PM (eds) The molecular and cellular biology of wound repair. Plenum Press, New York, pp 471–496

    Google Scholar 

  • Van den Hoff A (1988) Stromal involvement in malignant growth. Adv Cancer Res 50:159–196

    Google Scholar 

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

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

B. Czernobilsky was on sabbatical leave from the Department of Pathology, Kaplan Hospital, Rehovot, Israel

Rights and permissions

Reprints and permissions

About this article

Cite this article

Czernobilsky, B., Remadi, S. & Gabbiani, G. Alpha-smooth muscle actin and other stromal markers in endometrial mucosa. Vichows Archiv A Pathol Anat 422, 313–317 (1993). https://doi.org/10.1007/BF01608341

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01608341

Key words

Navigation