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The cytoskeleton of chick retinal pigment epithelial cells in situ

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Gelatin-coated slides were used to obtain en face preparations of retinal pigment epithelium (RPE) from 6-to 21-day-old chick embryos in order to study the distribution of F-actin in microfilaments (MF) and the MF-associated proteins, myosin, tropomyosin,α-actinin and vinculin in situ at different stages of development by fluorescence microscopy. The epithelial sheets were fixed in formaldehyde and then extracted in a solution containing 0.1% Triton X-100. NBD-Phallacidin was used to visualize the F-actin in MF, and antisera against myosin, tropomyosin,α-actinin and vinculin were used to determine the distribution of these four MF-associated proteins. F-actin, myosin, tropomyosin,α-actinin and vinculin were present in cortical rings around the apical ends of the RPE cells throughout this period of development. Of these proteins, only F-actin was identified in the apical processes of RPE cells. The increase in the amount of F-actin could be followed as the length and the number of apical processes increased with age and maturation of RPE cells. F-actin was first detected in numerous short apical processes on the surface of each RPE cell on day 12. From day 12 to day 17, they were at an intermediate stage of elongation and from day 17 onward all of the RPE cells had long F-actin-containing apical processes. These results indicate that the F-actin-containing MF assemble much later in the apical processes than in the cortical rings. Also the cortical rings and apical processes of RPE cells resemble those in absorptive intestinal cells in that the cortical rings in both cell types contain MF associated with myosin, tropomyosin,α-actinin and vinculin while the MF in the apical processes and microvilli lack these MF associated proteins, and both of these structures lack talin. In addition to apical processes and cortical rings, stained fibers were also observed at a level below the cortical rings. The simple and highly reproducible en face method described is useful for determining changes in the organization of cytoskeletal components and other macromolecules in RPE cells and other epithelial cells in situ.

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References

  • Barak LS, Yocum RR, Nothnagel RR, Webb WW (1980) Fluorescence staining of the actin cytoskeleton in living cells with 7-nitrobenz-2-oxa-1,3-diazole-phallacidin. Proc Natl Acad Sci USA 77:980

    PubMed  Google Scholar 

  • Bretscher A (1983) Microfilament organization in the cytoskeleton of the intestinal brush border. In: Dowben RM, Shay JW (eds) Cell and Muscle Motility. Plenum Press, New York, Vol 4, pp 239–268

    Google Scholar 

  • Bretscher A, Weber K (1978) Localization of actin and microfilament-associated proteins in microvilli and terminal web of the intestinal brush border by immunofluorescence microscopy. J Cell Biol 79:839–845

    PubMed  Google Scholar 

  • Buck RC (1979) Cell migration in repair of mouse corneal epithelium. Invest Ophthal Vis Sci 18:767–784

    PubMed  Google Scholar 

  • Burnside B, Laties AM (1976) Actin filaments in apical projections of the primate pigmented epithelial cells. Invest Ophthalmol 15:570–575

    PubMed  Google Scholar 

  • Burnside B, Laties A (1979) Pigment movement and cellular contractility in the retinal pigment epithelium. In: Zinn KM, Marmor MF (eds) The Retinal Pigment Epithelium. Harvard University Press, Cambridge, pp 175–191

    Google Scholar 

  • Burridge K, Connell L (1983) Talin: A cytoskeletal component concentrated in adhesion plaques and other sites of actin-membrane interaction. Cell Motil 3:405–417

    PubMed  Google Scholar 

  • Crawford B (1979) Cloned pigmented retinal epithelium: the role of microfilaments in the differentiation of cell shape. J Cell Biol 81:301–315

    PubMed  Google Scholar 

  • Crawford B, Cloney RA, Cahn RD (1972) Cloned pigmented retinal cells; the affects of cytochalasin B on ultratructure and behaviour. Z Zellforsch 130:135–151

    PubMed  Google Scholar 

  • Drenckhahn D, Groschel-Stewart U (1980) Localization of myosin, actin and tropomyosin in rat intestinal epithelium: Immunohistochemical studies at the light and electron microscope levels. J Cell Biol 86:475–482

    PubMed  Google Scholar 

  • Drenckhahn D, Wagner H-J (1985) Relation of retinomotor responses and contractile proteins in vertebrate retinas. Eur J Cell Biol 37:156–168

    PubMed  Google Scholar 

  • Geiger B, Dutton AH, Tokuyasu KT, Singer SJ (1981) Immunoelectron microscopic studies of membrane-microfilament interactions: Distributions of α-actinin, tropomyosin, and vinculin in intestinal epithelial brush border and chicken gizzard smooth muscle cells. J Cell Biol 91:614–628

    PubMed  Google Scholar 

  • Geiger B (1983) Membrane-cytoskeleton interaction. Biochim Biophys Acta 737:305–341

    PubMed  Google Scholar 

  • Gotlieb AI, Spector W (1981) Migration into an in vitro experimental wound. A comparison of porcine aortic endothelial and smooth muscle cells and the effect of culture irradiation. Am J Pathol 103:271–282

    PubMed  Google Scholar 

  • Hirokawa N, Keller TCS, Chasen R, Mooseker MS (1983) Mechanism of brush border contractility studies by the quick-freeze, deep etch method. J Cell Biol 96:1325–1336

    PubMed  Google Scholar 

  • Hirokawa N, Tilney LG, Fujiwara K, Heuser JE (1982) Organization of actin, myosin and intermediate filaments in the brush border of intestinal epithelial cells. J Cell Biol 94:425–443

    PubMed  Google Scholar 

  • Honda H (1983) Geometric models for cells in tissues. Int Rev Cytol 81:191–254

    PubMed  Google Scholar 

  • Honda H, Eguchi G (1980) How much does the cell boundary contrast in a monolayered cell sheet? J Theor Biol 84:575–588

    PubMed  Google Scholar 

  • Jacobson BS (1983) Interaction of the plasma membrane with the cytoskeleton: a review. Tissue Cell 15:829–852

    PubMed  Google Scholar 

  • Johnson GD, Davidson RS, McNamee KC, Russel G, Goodwin D, Holborow EJ (1982) Fading of immunofluorescence during microscopy: A study of the phenomenon and its remedy. J Immunol Methods 55:231–242

    PubMed  Google Scholar 

  • Jorgensen AO, Subrahmanyan L, Kamins VI (1975) Localization of tropomyosin in mouse embryo fibroblasts. Am J Anat 142:519–525

    PubMed  Google Scholar 

  • Mooseker MS (1983) Actin bunding proteins of the brush border. Cell 35:11–13

    PubMed  Google Scholar 

  • Mooseker NS, Bonder ME, Conzelman KA, Fishkind DJ, Howe CL, Keller CS (1984) Brush border cytoskeleton and integration of cellular functions. J Cell Biol 99:1045–1125

    PubMed  Google Scholar 

  • Murray RL, Dubin MW (1975) The occurrence of actin-like filaments in association with migrating pigment granules in frog retinal pigment epithelium. J Cell Biol 64:705–710

    PubMed  Google Scholar 

  • Nguyen-Legros J (1978) Fine structure of the pigment epithelium in the vertebrate retina. Int Rev Cytol [Suppl] 7:287–328

    Google Scholar 

  • Opas M (1985) The focal adhesions of chick retinal pigmented epithelial cells. Can J Biochem Cell Biol 63:553–563

    PubMed  Google Scholar 

  • Opas M, Kalnins VI (1985) Spatial distribution of cortical porteins in cells of epithelial sheets. Cell Tissue Res 239:451–454

    PubMed  Google Scholar 

  • Opas M, Turksen K, Kalnins VI (1985) Adhesiveness and distribution of vinculin and spectrin in retinal pigmented epithelial cells during growth and differentiation in vitro. Dev Biol 107:269–280

    PubMed  Google Scholar 

  • Owaribe K, Eguchi G (1984) Increase in actin contents and elongation of microvilli in retinal pigment epithelial cells during development of the chicken eye. In: Seno S, Okada Y (eds) Intl Cell Biology Tokyo. Academic Press, Tokyo, p 473a

    Google Scholar 

  • Owaribe K, Eguchi G (1985) Increase in actin contents and elongation of apical projections in retinal pigmented epithelial cells during development of the chicken eye. J Cell Biol 101:590–596

    PubMed  Google Scholar 

  • Owaribe K, Masuda H (1982) Isolation and characterization of circumferential microfilament bundles from retinal pigmented epithelial cells. J Cell Biol 95:310–315

    PubMed  Google Scholar 

  • Owaribe K, Araki M, Hatano S (1979) Cell shape and actin filaments. In: Hatano S, Ishikawa H, Sato H (eds) Cell Motility: Molecules and Organization. University of Tokyo Press, Tokyo, pp 491–500

    Google Scholar 

  • Owaribe K, Kodama R, Eguchi G (1981) Demonstration of contractility of circumferential actin bundles and its morphogenic significance in pigmented epithelium in vitro and in vivo. J Cell Biol 90:507–514

    PubMed  Google Scholar 

  • Philp NJ, Nachmias VT (1985) Components of the cytoskeleton in the retinal pigmented epithelium of the chick. J Cell Biol 101:358–362

    PubMed  Google Scholar 

  • Rogers KA, Kalnins VI (1984) Comparison of the cytoskeleton in aortic endothelial cells in situ and in vitro. Lab Invest 39:650–654

    Google Scholar 

  • Stein MB, Gordon R (1982) Epithelia as bubble rafts: A new method for analysis of cell shape and intercellular adhesion in embryonic and other epithelia. J Theor Biol 97:625–639

    PubMed  Google Scholar 

  • Turksen K, Opas M, Aubin JE, Kalnins VI (1983) Microtubulues, microfilaments and adhesion patterns in differentiation chick retinal pigment epithelial (RPE) cells in vitro. Exp Cell Res 147:379–391

    PubMed  Google Scholar 

  • Zinn KM, Benjamin-Henkind J (1982) The retinal pigment epithelium. In: Jakobiel FA (ed) Ocular Anatomy, Embryology and Teratology. Harper and Rowe, Philadelphia, pp 533–552

    Google Scholar 

  • Zinn KM, Marmor MF (1979) The retinal pigment epithelium. Harvard University Press, Cambridge

    Google Scholar 

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Turksen, K., Kalnins, V.I. The cytoskeleton of chick retinal pigment epithelial cells in situ. Cell Tissue Res. 248, 95–101 (1987). https://doi.org/10.1007/BF01239968

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