The fine structure of the haemocyte of the holothurian, Cucumaria miniata (Brandt)

1973 ◽  
Vol 51 (3) ◽  
pp. 323-332 ◽  
Author(s):  
A. R. Fontaine ◽  
Philip Lambert

The fine structure of the holothurian haemocyte is similar to that of the nucleated erythrocytes of lower vertebrates. Points of similarity include nuclear and nucleolar features, the distribution of haemoglobin, mitochondria, lysosomes, Golgi apparatus, and centrioles, and the presence of a marginal band of microtubules. Features apparently unique to this haemocyte are a canalicular system and an isolation membrane system. An interpretation of the functional relationships of the organelles is presented. Stages in the development and degradation of the haemocyte are also demonstrated. The morphological similarity of the holothurian haemocyte to lower vertebrate erythrocytes is attributed to functional analogy and parallel cellular adaptations, but not to homology.

Cell ◽  
2008 ◽  
Vol 133 (6) ◽  
pp. 1055-1067 ◽  
Author(s):  
George H. Patterson ◽  
Koret Hirschberg ◽  
Roman S. Polishchuk ◽  
Daniel Gerlich ◽  
Robert D. Phair ◽  
...  

Parasitology ◽  
1975 ◽  
Vol 70 (2) ◽  
pp. 223-229 ◽  
Author(s):  
E. Michael

The fine structure of trophozoites, schizonts, merozoites and macrogamonts of Eimeria acervulina found in goblet cells of the duodenal epithelium of chicks is described and compared with the corresponding stages formed in other epithelial cells. Complete schizogony, with the formation of mature merozoites, occurred freely in goblet cells. Developing macrogamonts (but no microgamonts) were rarely found in goblet cells. The stages observed were confined to the cytoplasm of the host cell above the Golgi apparatus and were usually seen between the mucous granules. The stages seen appeared normal, and contained similar structures to corresponding stages developing in other cells. The finding of developing stages of E. acervulina in goblet cells provides further evidence that site specificity of Eimeria at the cellular level is not as strict as previously thought.


1974 ◽  
Vol 14 (3) ◽  
pp. 633-655
Author(s):  
EVA KONRAD HAWKINS

The fine structure of the Golgi apparatus during development of tetrasporangia of Calli-thamnion roseum is described. Dictyosomes and associated vesicles of 4 developmental stages of sporangia are examined. The wall of sporangia exhibits a heretofore unseen cuticle in red algae. Development of the spore wall and a new plasma membrane around spores occurs through fusion of adjacent Golgi vesicles along the periphery of cells. Observations are discussed in relation to wall formation and expansion of tetrads and in comparison with other work on growth and differentiation of the Golgi apparatus.


1965 ◽  
Vol s3-106 (73) ◽  
pp. 15-21
Author(s):  
JOHN R. BAKER

The exocrine cells of the mouse pancreas were fixed in potassium dichromate solution, embedded in araldite or other suitable medium, and examined by electron microscopy. Almost every part of these cells is seriously distorted or destroyed by this fixative. The ergastoplasm is generally unrecognizable, the mitochondria and zymogen granules are seldom visible, and no sign of the plasma membrane, microvilli, or Golgi apparatus is seen. The contents of the nucleus are profoundly rearranged. It is seen to contain a large, dark, irregularly shaped, finely granular object; the evidence suggests that this consists of coagulated histone. The sole constituent of the cell that is well fixed is the inner nuclear membrane. The destructive properties of potassium dichromate are much mitigated when it is mixed in suitable proportions with osmium tetroxide or formaldehyde.


1984 ◽  
Vol 66 (1) ◽  
pp. 175-187
Author(s):  
M. Fukumoto

The apical structure in Perophora annectens spermatozoa is approximately 4 micron in length and it is helically coiled. Its major component is a striated structure, which may be analogous to a perforatorium. The plasmalemma enclosing the anterior quarter of the apical structure is covered by extracellular materials, the anterior ornaments. During spermiogenesis, the apical structure is first recognized as a small blister of the plasmalemma at the apex of the young spermatid. It develops into a conical protrusion and then into a finger-like process (approximately 1 micron in length). This process is transformed into an elongated process (approximately 4 micron in length) with electron-dense material in its core. Finally, the elongated process is helically coiled to form an apical structure in which electron-dense material forms dense striations. Vesicles (50-70 nm in diameter), presumably derived from the Golgi apparatus, have been recognized in the blisters of younger spermatids, and can be followed through to the finger-like process. In the finger-like process these vesicles are transformed into smaller vesicles (20-30 nm in diameter), which probably fuse with the anterior plasmalemma of the finger-like process. This suggests that chorion lysin(s) is associated with the anterior membrane enclosing the apical structure in these spermatozoa.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Yan-Mei Chen ◽  
Edward C. Holmes ◽  
Xiao Chen ◽  
Jun-Hua Tian ◽  
Xian-Dan Lin ◽  
...  

Abstract Despite increasing evidence that antibiotic resistant pathogens are shared among humans and animals, the diversity, abundance and patterns of spread of antibiotic resistance genes (ARGs) in wildlife remains unclear. We identified 194 ARGs associated with phenotypic resistance to 13 types of antibiotic in meta-transcriptomic data generated from a broad range of lower vertebrates residing in both terrestrial and aquatic habitats. These ARGs, confirmed by PCR, included those that shared high sequence similarity to clinical isolates of public health concern. Notably, the lower vertebrate resistome varied by ecological niche of the host sampled. The resistomes in marine fish shared high similarity and were characterized by very high abundance, distinct from that observed in other habitats. An assessment of ARG mobility found that ARGs in marine fish were frequently co-localized with mobile elements, indicating that they were likely spread by horizontal gene transfer. Together, these data reveal the remarkable diversity and transcriptional levels of ARGs in lower vertebrates, and suggest that these wildlife species might play an important role in the global spread of ARGs.


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