Literature DB >> 8314842

Phagocytosis induced by thyrotropin in cultured thyroid cells is associated with myosin light chain dephosphorylation and stress fiber disruption.

W J Deery1, J P Heath.   

Abstract

The actin/myosin II cytoskeleton and its role in phagocytosis were examined in primary cultures of dog thyroid cells. Two (19 and 21 kD) phosphorylated light chains of myosin (P-MLC) were identified by two-dimensional gel electrophoresis of antimyosin immunoprecipitates, and were associated with the Triton X-100 insoluble, F-actin cytoskeletal fraction. Analyses of Triton-insoluble and soluble 32PO4-prelabeled protein fractions indicated that TSH (via cAMP) or TPA treatment of intact cells decreases the MLC phosphorylation state. Phosphoamino acid and tryptic peptide analyses of 32P-MLCs from basal cells showed phosphorylation primarily at threonine and serine residues; most of the [32P] appeared associated with a peptide containing sites typically phosphorylated by MLC kinase. Even in the presence of the agents which induced dephosphorylation, the phosphatase inhibitor, calyculin A, caused a severalfold increase in MLC phosphorylation at several distinct serine and threonine sites which was also associated with actomyosin and cell contraction. Phosphorylation of cell homogenate proteins or the cytoskeletal fraction with [gamma-32P]ATP indicated that Ca2+, EGTA, or trifluoperazine (TFP) has little effect on the phosphorylation of MLC. Both fluorescent phalloidin and antimyosin staining of cells showed distinct dorsal and ventral stress fiber complexes which were disrupted within 30 min by TSH and cAMP; TPA appeared to cause disruption of dorsal, and rearrangement of ventral complexes. Concomitant with MLC dephosphorylation and stress fiber disruption, TSH/cAMP, but not TPA, induced dorsal phagocytosis of latex beads. While stimulation of either A or C-kinase disrupts dorsal stress fibers and rearranges actomyosin, another event(s) mediated by A-kinase appears necessary for phagocytic activity.

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Year:  1993        PMID: 8314842      PMCID: PMC2119617          DOI: 10.1083/jcb.122.1.21

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


  52 in total

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Authors:  T D Pollard; S K Doberstein; H G Zot
Journal:  Annu Rev Physiol       Date:  1991       Impact factor: 19.318

2.  Morphological and biochemical responses of cultured thyroid cells to thyrotropin.

Authors:  T B Nielsen; M S Ferdows; B R Brinkley; J B Field
Journal:  Endocrinology       Date:  1985-02       Impact factor: 4.736

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Authors:  W F Harrington; M E Rodgers
Journal:  Annu Rev Biochem       Date:  1984       Impact factor: 23.643

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Journal:  FEBS Lett       Date:  1984-03-12       Impact factor: 4.124

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Authors:  H A Cole; H S Griffiths; V B Patchell; S V Perry
Journal:  FEBS Lett       Date:  1985-01-28       Impact factor: 4.124

6.  Phosphorylation of smooth muscle myosin light chain kinase by Ca2+-activated, phospholipid-dependent protein kinase.

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Journal:  J Biol Chem       Date:  1985-04-25       Impact factor: 5.157

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Journal:  J Biol Chem       Date:  1983-11-10       Impact factor: 5.157

8.  Interaction of tumour promoters with epithelial cells in culture. An immunofluorescence study.

Authors:  S Kellie; T C Holme; M J Bissell
Journal:  Exp Cell Res       Date:  1985-10       Impact factor: 3.905

9.  A tumor promoter induces rapid and coordinated reorganization of actin and vinculin in cultured cells.

Authors:  M Schliwa; T Nakamura; K R Porter; U Euteneuer
Journal:  J Cell Biol       Date:  1984-09       Impact factor: 10.539

10.  Light chain phosphorylation regulates the movement of smooth muscle myosin on actin filaments.

Authors:  J R Sellers; J A Spudich; M P Sheetz
Journal:  J Cell Biol       Date:  1985-11       Impact factor: 10.539

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  5 in total

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Authors:  Jun Yang; Shasha Yin; Fangfang Bi; Lin Liu; Tian Qin; Hongwei Wang; Wangsen Cao
Journal:  J Mol Med (Berl)       Date:  2016-10-06       Impact factor: 4.599

2.  Morphology of Drosophila S-2 cells in different culture conditions.

Authors:  L Søndergaard
Journal:  In Vitro Cell Dev Biol Anim       Date:  1994-01       Impact factor: 2.416

3.  G protein α12 (Gα12) is a negative regulator of kidney injury molecule-1-mediated efferocytosis.

Authors:  Ola Z Ismail; Xizhong Zhang; Joseph V Bonventre; Lakshman Gunaratnam
Journal:  Am J Physiol Renal Physiol       Date:  2015-12-23

4.  Apoptotic membrane blebbing is regulated by myosin light chain phosphorylation.

Authors:  J C Mills; N L Stone; J Erhardt; R N Pittman
Journal:  J Cell Biol       Date:  1998-02-09       Impact factor: 10.539

5.  Persistent cAMP-signals triggered by internalized G-protein-coupled receptors.

Authors:  Davide Calebiro; Viacheslav O Nikolaev; Maria Cristina Gagliani; Tiziana de Filippis; Christian Dees; Carlo Tacchetti; Luca Persani; Martin J Lohse
Journal:  PLoS Biol       Date:  2009-08-18       Impact factor: 8.029

  5 in total

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