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Mechanisms of nutritive endocytosis. III. A freeze-fracture study of phagocytosis by digestive cells of Chlorohydra

  • Paul L. McNeil(corresponding author)
*Corresponding author for this work
  • University of California at Los Angeles
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Freeze-fracturc was used to compare the ultrastructure of plasma with phagosomal membranes of digestive cells of green hydra. Changes in both the pattern and density of intramembrane particles (IMP) were evident during the transition from plasma to phagosomal membrane. Small particle-free regions and associated aggregates of three to eight IMP were observed in presumptive adherent and enveloping plasma membranes, as well as in fully formed phagosomal membranes. Larger particle-free regions were observed as rims around the tips of enveloping membranes which had nearly completed enclosure of particles. The density of IMP in newly formed phagosomal membranes was 1.5-fold greater than that in the parent plasma membrane from which they derived, and was greater also than in older phagosomal membranes.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 519-533 (15 pages)

Journal (Volume, Issue Number)

Tissue and Cell (Volume 16, Issue 4)

Publication milestones

  • Published - 1984

Publication status

Published - 1984

ISSN

0040-8166

Publication IDs

  • Scopus: 0021156195
  • PubMed: 6484935

Publication metrics

Metrics

Fractional count
1
Fractional count
1
Fractional count
1
Fractional count
1
Scopus
citations

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Captures
12
Citation count
14

Funding Details

I thank Dr L. Muscatinef or advice, support and encouragementD; rs J. Frank and F. S. Sjostrand for critical appraisal of this work and for generous provision of laboratory facilities; and MS J. Baumer, MS S. Beydler and Mr H. Kabe for their excellent technical help. The researchw ass upported,in part, by grantsf rom the National ScienceF oundation (PCM 75-03380a nd PCM 78-27380)a nd a UCLA Biomedical ResearchS upport Grant (USPHS 5-507R R 07009-14)b, oth to Dr L. Muscatine.
FundersFunding numbers
National ScienceF oundation
PCM 75-03380a, PCM 78-27380
UCLA
USPHS 5-507R R 07009-14