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Blebbing of Dictyostelium cells in response to chemoattractant

*Corresponding author for this work
  • Medical Research Council
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Stimulation of Dictyostelium cells with a high uniform concentration of the chemoattractant cyclic-AMP induces a series of morphological changes, including cell rounding and subsequent extension of pseudopodia in random directions. Here we report that cyclic-AMP also elicits blebs and analyse their mechanism of formation. The surface area and volume of cells remain constant during blebbing indicating that blebs form by the redistribution of cytoplasm and plasma membrane rather than the exocytosis of internal membrane coupled to a swelling of the cell. Blebbing occurs immediately after a rapid rise and fall in submembraneous F-actin, but the blebs themselves contain little F-actin as they expand. A mutant with a partially inactivated Arp2/3 complex has a greatly reduced rise in F-actin content, yet shows a large increase in blebbing. This suggests that bleb formation is not enhanced by the preceding actin dynamics, but is actually inhibited by them. In contrast, cells that lack myosin-II completely fail to bleb. We conclude that bleb expansion is likely to be driven by hydrostatic pressure produced by cortical contraction involving myosin-II. As blebs are induced by chemoattractant, we speculate that hydrostatic pressure is one of the forces driving pseudopod extension during movement up a gradient of cyclic-AMP. Crown

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 2009-2017 (9 pages)

Journal (Volume, Issue Number)

Experimental Cell Research (Volume 312, Issue 11)

Publication milestones

  • Published - 07/01/2006

Publication status

Published - 07/01/2006

ISSN

0014-4827

Publication IDs

  • Scopus: 33744902873
  • PubMed: 16624291

Publication metrics

Metrics

Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1
SciVal
FWCI
1.31
SciVal
Author count
2
SciVal
citations
70
SciVal
Paper percentile
92
SciVal
Top percentile
10
Scopus
citations

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Captures
83
Citation count
80

Funding Details

Many thanks to Rudy Behnia, David Traynor, Oliver Hoeller, Peter Lawrence and Richard Grenfell for discussions and/or technical assistance. PDL was supported by a studentship from the Medical Research Council.