Literature DB >> 6250703

Hormone-induced filopodium formation and movement of pigment, carotenoid droplets, into newly formed filopodia.

S J Lo, T T Tchen, J D Taylor.   

Abstract

Treatment of cultured goldfish xanthophores by hormone (ACTH) or c-AMP induces not only pigment dispersion, but subsequent outgrowth of processes, and pigment translocation into these processes. These latter effects are shown to proceed as follows: First the edge of the cytoplasmic lamellae takes on a scalloped contour with numerous protrusions. These presumably serve as nucleation centers where short microfilament bundles are assembled. Later, the microfilament bundles elongate ("grow"), often resulting in an extension of the protrusions to become filopodia while the proximal end of the microfilaments penetrates into the thicker portion of the cellular process which now houses the pigment, i.e., the carotenoid droplets. Carotenoid droplets appear to migrate along the microfilament bundles, or cytoplasmic channels associated with them, into the filopodia. Finally, some of the filopodia become broader, thicker and laden with carotenoid droplets and are then recognized by light microscopy as pigmented cellular processes. The microfilaments have been shown to be actin filaments by their thickness, the size of their subunits, and decoration by heavy meromyosin. Evidence is presented which suggests that the growth of these actin filaments may come about by recruitment from short F-actin strands found in random orientation in adjacent areas.

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Year:  1980        PMID: 6250703     DOI: 10.1007/bf00220195

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  34 in total

Review 1.  Cyclic AMP and cell behavior in cultured cells.

Authors:  M C Willingham
Journal:  Int Rev Cytol       Date:  1976

2.  Formation of filopodia in coelomocytes: localization of fascin, a 58,000 dalton actin cross-linking protein.

Authors:  J J Otto; R E Kane; J Bryan
Journal:  Cell       Date:  1979-06       Impact factor: 41.582

3.  Pigment movements in fish melanophores: morphological and physiological studies.

Authors:  M Schliwa; J Bereiter-Hahn
Journal:  Z Zellforsch Mikrosk Anat       Date:  1973-12-31

4.  Stereo high voltage electron microscopy of melanophores. Matrix transformations during pigment movements and the effects of cold and colchicine.

Authors:  M Schliwa
Journal:  Exp Cell Res       Date:  1979-02       Impact factor: 3.905

5.  Cytochalasin B reversibly inhibits melanin granule movement in melanocytes.

Authors:  S E Malawista
Journal:  Nature       Date:  1971-12-10       Impact factor: 49.962

6.  Hormone-induced pigment translocations in amphibian dermal iridophores, in vitro: changes in cell shape.

Authors:  B T Butman; M Obika; T T Tchen; J D Taylor
Journal:  J Exp Zool       Date:  1979-04

7.  Actin filament destruction by osmium tetroxide.

Authors:  P Maupin-Szamier; T D Pollard
Journal:  J Cell Biol       Date:  1978-06       Impact factor: 10.539

8.  Hormone-induced dispersion or aggregation of carotenoid-containing smooth endoplasmic reticulum in cultured xanthophores from the goldfish, Carrassius auratus L.

Authors:  J D Winchester; F Ngo; T T Tchen; J D Taylor
Journal:  Endocr Res Commun       Date:  1976

9.  Actin microfilaments in melanophores of Fundulus heteroclitus. Their possible involvement in melanosome migration.

Authors:  M Obika; D G Menter; T T Tchen; J D Taylor
Journal:  Cell Tissue Res       Date:  1978-10-30       Impact factor: 5.249

10.  Factors controlling the reassembly of the microvillous border of the small intestine of the salamander.

Authors:  L G Tilney; R R Cardell
Journal:  J Cell Biol       Date:  1970-11-01       Impact factor: 10.539

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  1 in total

1.  Purification of Black Moor goldfish melanophores and responses to epinephrine.

Authors:  C R Clark; J D Taylor; T T Tchen
Journal:  In Vitro Cell Dev Biol       Date:  1987-06
  1 in total

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