Abstract
The surface complex of Euglena has been examined intact and after isolation and purification by the use of mild sonication to disrupt cells. In intact cells the surface complex (pellicle complex) is oriented in a series of parallel ridges and grooves, and possesses among other components a characteristic group of four to seven microtubules. Isolated pellicles retain the ridge and groove pattern but no microtubules are present. Isolates yielded at least three major polypeptides on SDS acrylamide gels; one or more of the polypeptides are postulated to be identical with a submembrane layer present in both intact and isolated pellicles; one polypeptide appears to be in or on the surface membrane. Antibodies directed against the isolated pellicles were conjugated directly or indirectly to fluorescein, latex spheres, or ferritin. In appropriate experiments with these antibody conjugates, it has been found that antigenic sites are immobile and that new antigenic sites (daughter strips) are inserted between parental strips in replicating cells. These results together with direct observation of daughter strips by transmission electron microscopy suggest that surface growth in Euglena occurs by intussusception. Microtubules associated with the pellicle complex are postulated to play a role in the development of new daughter strips, and possibly also in cell movements.
MeSH Terms
Antigens
Carbohydrates/analysis
Cell Division
Cell Fractionation
Cell Membrane/immunology,ultrastructure
Euglena gracilis/growth & development,ultrastructure
Fluorescent Antibody Technique
Lipids/analysis
Microtubules/physiology,ultrastructure
Models, Biological
Proteins/analysis,physiology
Chemicals
Antigens
Carbohydrates
Lipids
Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hofmann C
Bouck G B
References (24)
24 references, click to expand
-
THE ULTRASTRUCTURE OF THE PELLICLE COMPLEX OF EUGLENA GRACILIS.
J Cell Biol. 1965 Feb;24:253-7
PMID: 14326110
-
PELLICULAR CHANGES DURING DIVISION IN ASTASIA LONGA.
Exp Cell Res. 1964 Jul;35:423-5
PMID: 14195451
-
Isolated cilia from Tetrahymena pyriformis.
Exp Cell Res. 1962 Nov;28:280-95
PMID: 13999215
-
The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.
J Cell Biol. 1963 Apr;17:208-12
PMID: 13986422
-
Protein measurement with the Folin phenol reagent.
J Biol Chem. 1951 Nov;193(1):265-75
PMID: 14907713
-
The rapid intermixing of cell surface antigens after formation of mouse-human heterokaryons.
J Cell Sci. 1970 Sep;7(2):319-35
PMID: 4098863
-
Simple method for quantitive densitometry of polyacrylamide gels using fast green.
Anal Biochem. 1970 Jun;35(2):359-70
PMID: 4194859
-
Normal distribution, patching and capping of lymphocyte surface immunoglobulin studied by electron microscopy.
Nat New Biol. 1973 Feb 28;241(113):257-9
PMID: 4540373
-
Movement of lymphocyte surface antigens and receptors: the fluid nature of the lymphocyte plasma membrane and its immunological significance.
Fed Proc. 1973 Jan;32(1):48-54
PMID: 4119366
-
Anionic sites of human erythrocyte membranes. II. Antispectrin-induced transmembrane aggregation of the binding sites for positively charged colloidal particles.
J Cell Biol. 1973 Nov;59(2 Pt 1):395-406
PMID: 4141707
-
The fluid mosaic model of the structure of cell membranes.
Science. 1972 Feb 18;175(4023):720-31
PMID: 4333397
-
Effect of colchicine, colcemid, and vinblastine on the agglutination, by concanavalin A, of transformed cells.
Science. 1972 Nov 24;178(4063):867-8
PMID: 4343698
-
Membrane proteins.
Annu Rev Biochem. 1972;41:731-52
PMID: 4263713
-
Microtubules.
Annu Rev Biochem. 1973;42:507-40
PMID: 4581232
-
Fluidity of the surface of cultured muscle fibers. Rapid lateral diffusion of marked surface antigens.
J Cell Biol. 1973 Apr;57(1):27-37
PMID: 4570791
-
Microtubule biogenesis and cell shape in Ochromonas. II. The role of nucleating sites in shape development.
J Cell Biol. 1973 Feb;56(2):360-78
PMID: 4682901
-
Microtubule biogenesis and cell shape in Ochromonas. I. The distribution of cytoplasmic and mitotic microtubules.
J Cell Biol. 1973 Feb;56(2):340-59
PMID: 4682900
-
A low-viscosity epoxy resin embedding medium for electron microscopy.
J Ultrastruct Res. 1969 Jan;26(1):31-43
PMID: 4887011
-
Cell division in Astasia longa.
Exp Cell Res. 1965 Sep;39(2):504-27
PMID: 5320214
-
Topography of lymphocyte surface immunoglobulin using scanning immunoelectron microscopy.
J Ultrastruct Res. 1975 Apr;51(1):55-68
PMID: 1092883
-
Ultrastructural localization of the high molecular weight proteins associated with in vitro-assembled brain microtubules.
J Cell Biol. 1975 Apr;65(1):237-41
PMID: 1127013
-
Arms and bridges on microtubules in the mitotic apparatus.
J Cell Biol. 1969 Mar;40(3):854-9
PMID: 5765772
-
Observations on the fine structure of the pellicle pores of Euglena granulata.
Protoplasma. 1967;64(3):330-44
PMID: 6081636
-
Microtubules in the spermatids of the domestic fowl.
J Cell Biol. 1967 Oct;35(1):153-73
PMID: 6061713