Mechanisms of nutritive endocytosis i. phagocytic versatility and cellular recognition in Chlorohydra digestive cells, a scanning electron microscope study
Open Access
- 1 June 1981
- journal article
- research article
- Published by The Company of Biologists in Journal of Cell Science
- Vol. 49 (1) , 311-339
- https://doi.org/10.1242/jcs.49.1.311
Abstract
The quantity of surface membrane internalized during phagocytosis by Chlorohydra digestive cells was estimated for a range of particle types. Challenge with 2 of these particles, freshly isolated symbiotic algae (FIS) and latex spheres (LS), resulted in a greater (2·5 ×) quantity of surface membrane interiorized than with heat-treated symbiotic algae (HTS) and free living algae (FA), Chlorella vulgaris. This discriminatory process was investigated further by a scanning electron microscope (SEM) and transmission electron microscope (TEM) comparison of the surface events associated with phagocytosis of each of these 4 particles. Those particles that were avidly phagocytized, FIS and LS, were both enveloped by a tightly fitting extension of digestive-cell surface, and obtained a prominent surface coating after their injection into the gut of Chlorohydra. Phagocytic challenge with FIS resulted, furthermore, in the rapid formation of a dense microvillar cover on digestive-cell surfaces. HTS and FA, on the other hand, were enveloped by a less closely fitting extension of digestive-cell surface, did not obtain a prominent surface coating, and did not induce the formation of microvilli. In addition, SEM revealed that at least 3 morphologically distinct phagocytic modes were utilized by the versatile nutritive phagocyte of Chlorohydra’. (1) envelopment by the progressive movement of numerous, overlapping tubular protrusions (microvilli) over the particle (FIS) surface, forming first a network of tubular interlocking members, and finally a continuous but rough enclosing surface; (2) envelopment by a single, smooth-surfaced, funnel-like extension of digestive-cell surface (FIS, LS, HTS, FA); and (3) envelopment by multiple, broad folds, often of unequal size, and with overlapping margins (Artemia particles).This publication has 25 references indexed in Scilit:
- A low-viscosity epoxy resin embedding medium for electron microscopyPublished by Elsevier ,2004
- Distribution of actin-binding protein and myosin in macrophages during spreading and phagocytosis.The Journal of cell biology, 1980
- EndocytosisAnnual Review of Biochemistry, 1977
- Studies on the mechanism of phagocytosis. II. The interaction of macrophages with anti-immunoglobulin IgG-coated bone marrow-derived lymphocytes.The Journal of Experimental Medicine, 1976
- The surface morphology of the phagocytosis of micro-organisms by peritoneal macrophagesThe Journal of Pathology, 1976
- Localization of receptors and early events of phagocytosis in the macrophageExperimental Cell Research, 1975
- RECOGNITION OF SYMBIOTIC ALGAE BYHYDRA VIRIDIS.A QUANTITATIVE STUDY OF THE UPTAKE OF LIVING ALGAE BY APOSYMBIOTICH. VIRIDISThe Biological Bulletin, 1973
- A scanning electron microscopic study of phagocytosisExperimental Cell Research, 1971
- PHAGOCYTOSIS OF LATEX BEADS BY ACANTHAMOEBA The Journal of cell biology, 1967
- SYMBIOSIS OF HYDRA AND ALGAE. I. EFFECTS OF SOME ENVIRONMENTAL CATIONS ON GROWTH OF SYMBIOTIC AND APOSYMBIOTIC HYDRAThe Biological Bulletin, 1965