Literature DB >> 3793761

Development of a differentiated microtubule structure: formation of the chicken erythrocyte marginal band in vivo.

S Kim, M Magendantz, W Katz, F Solomon.   

Abstract

The microtubules of mature nucleated erythrocytes are organized into a marginal band that is confined to a single plane at the periphery and that contains essentially the same number of microtubule profiles in each individual cell. Developing erythrocytes can be isolated in homogeneous and synchronously developing populations from chicken embryos. For these reasons, these cells offer a particularly accessible system for study of the pathway leading to a specific microtubule structure in a normal, terminally differentiated animal cell. Along this developmental course, striking changes occur in the properties of the microtubules. Between the postmitotic cell and the formation of the band, a novel arrangement is found: bundles of laterally associated microtubules in each cell, coursing through the cytoplasm but not confined to the periphery. The microtubule organizing centers evident at early stages disappear by the time the band forms. The microtubules in early cells are readily depolymerized by drugs, but that drug sensitivity is lost in the mature cells. The microtubule arrangement of mature cells is faithfully recapitulated after reversible depolymerization, while that of the immature cells is not. Finally, as the band forms, the microtubules and microfilaments increasingly become coaligned. In sum, the microtubules of immature cells have many properties in common with those of cultured cells, but during maturation those properties change. The results suggest that lateral interactions become increasingly important in stabilizing and organizing the microtubules. The properties of marginal band microtubules, and comparable properties of axonal microtubules, may reflect differences between the requirements for cytoskeletal structures of cycling cells and terminally differentiated cells.

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Year:  1987        PMID: 3793761      PMCID: PMC2117030          DOI: 10.1083/jcb.104.1.51

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  26 in total

1.  Cytoplasmic microtubules in tissue culture cells appear to grow from an organizing structure towards the plasma membrane.

Authors:  M Osborn; K Weber
Journal:  Proc Natl Acad Sci U S A       Date:  1976-03       Impact factor: 11.205

2.  The display of microtubules in transformed cells.

Authors:  M Osborn; K Weber
Journal:  Cell       Date:  1977-11       Impact factor: 41.582

3.  Cytoplasmic microtubular images in glutaraldehyde-fixed tissue culture cells by electron microscopy and by immunofluorescence microscopy.

Authors:  K Weber; P C Rathke; M Osborn
Journal:  Proc Natl Acad Sci U S A       Date:  1978-04       Impact factor: 11.205

4.  The erythroid cells and haemoglobins of the chick embryo.

Authors:  G A Bruns; V M Ingram
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1973-10-25       Impact factor: 6.237

5.  The microtubule marginal band of the newt erythrocyte. Observations on the isolated band.

Authors:  B Bertolini; G Monaco
Journal:  J Ultrastruct Res       Date:  1976-01

6.  Identification with cellular microtubules of one of the co-assemlbing microtubule-associated proteins.

Authors:  F Solomon; M Magendantz; A Salzman
Journal:  Cell       Date:  1979-10       Impact factor: 41.582

7.  Neuroblastoma cells recapitulate their detailed neurite morphologies after reversible microtubule disassembly.

Authors:  F Solomon
Journal:  Cell       Date:  1980-09       Impact factor: 41.582

8.  Observations of the marginal band system of nucleated erythrocytes.

Authors:  W D Cohen
Journal:  J Cell Biol       Date:  1978-07       Impact factor: 10.539

9.  Tubulin assembly sites and the organization of cytoplasmic microtubules in cultured mammalian cells.

Authors:  B R Brinkley; S M Cox; D A Pepper; L Wible; S L Brenner; R L Pardue
Journal:  J Cell Biol       Date:  1981-09       Impact factor: 10.539

10.  Implications of treadmilling for the stability and polarity of actin and tubulin polymers in vivo.

Authors:  M W Kirschner
Journal:  J Cell Biol       Date:  1980-07       Impact factor: 10.539

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  11 in total

1.  A role for microtubule bundles in the morphogenesis of chicken erythrocytes.

Authors:  B Winckler; F Solomon
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-15       Impact factor: 11.205

Review 2.  The cytoskeletal mechanics of brain morphogenesis. Cell state splitters cause primary neural induction.

Authors:  R Gordon; G W Brodland
Journal:  Cell Biophys       Date:  1987-12

3.  Megakaryocyte lineage-specific class VI β-tubulin suppresses microtubule dynamics, fragments microtubules, and blocks cell division.

Authors:  Hailing Yang; Anutosh Ganguly; Shanghua Yin; Fernando Cabral
Journal:  Cytoskeleton (Hoboken)       Date:  2011-03

4.  Tyrosination-detyrosination of tubulin and microtubules during the development of chick erythrocytes.

Authors:  D M Beltramo; C A Arce; H S Barra
Journal:  Mol Cell Biochem       Date:  1989-08-15       Impact factor: 3.396

5.  Domains of beta-tubulin essential for conserved functions in vivo.

Authors:  J L Fridovich-Keil; J F Bond; F Solomon
Journal:  Mol Cell Biol       Date:  1987-10       Impact factor: 4.272

6.  Immunolocalization and molecular properties of a high molecular weight microtubule-bundling protein (syncolin) from chicken erythrocytes.

Authors:  P Feick; R Foisner; G Wiche
Journal:  J Cell Biol       Date:  1991-02       Impact factor: 10.539

7.  Detyrosination of alpha tubulin does not stabilize microtubules in vivo.

Authors:  D R Webster; J Wehland; K Weber; G G Borisy
Journal:  J Cell Biol       Date:  1990-07       Impact factor: 10.539

8.  The role of cytoskeleton in organizing growth cones: a microfilament-associated growth cone component depends upon microtubules for its localization.

Authors:  K Goslin; E Birgbauer; G Banker; F Solomon
Journal:  J Cell Biol       Date:  1989-10       Impact factor: 10.539

9.  Laser-transected microtubules exhibit individuality of regrowth, however most free new ends of the microtubules are stable.

Authors:  W Tao; R J Walter; M W Berns
Journal:  J Cell Biol       Date:  1988-09       Impact factor: 10.539

10.  Gelsolin is expressed in early erythroid progenitor cells and negatively regulated during erythropoiesis.

Authors:  H Hinssen; J Vandekerckhove; E Lazarides
Journal:  J Cell Biol       Date:  1987-09       Impact factor: 10.539

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