scholarly journals Visualization of cytoplasmic organelles via in-resin CLEM using an osmium-resistant far-red protein

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Isei Tanida ◽  
Soichiro Kakuta ◽  
Juan Alejandro Oliva Trejo ◽  
Yasuo Uchiyama
Author(s):  
Sant S. Sekhon

Although there have been numerous studies concerning the morphogenetic changes accompanying the maturation of insect sperm, only a few deal with the sperm differentiation in the dragonflies. In two recent electron microscopic studies Kessel, has comprehensively treated the erlationship of microtubules to the nucleus and mid-piece structures during spermiogenesis in the dragonfly. The purpose of this study is to follow the sequential nuclear and cytoplasmic changes which accompany the differentiation of spermatogonium into a mature sperm during spermatogenesis in the dragonfly (Aeschna sp.).The dragonfly spermatogonia are characterized by large round nuclei. Loosely organized chromatin is usually unevenly distributed within the spermatogonial nuclei. The scant cytoplasm surrounding the nucleus contains mitochondria, the Golgi apparatus, elements of endoplasmic reticulum and numerous ribosomes (Fig. 1).


Ovaries from eighty foetal and neonatal rats (aged 16·0 days post coitum to 4 days post partum ) were examined under the electron microscope. All the normal developmental stages (oogonia and oocytes in the leptotene, zygotene, pachytene, diplotene and dictyate phases of meiotic prophase) were identified. Patterns of degeneration (‘atretic divisions’, ‘ Z ’ cells and atresia at the diplotene phase), whose histological appearance and incidence have been recorded by Beaumont & Mandl (1962), were also recognized. The nuclei of oocytes at the leptotene phase contain single electron dense threads which become aligned in parallel pairs at the following phase (zygotene). A third finer fibril half-way between them appears at pachytene (tripartite ribbon). The longitudinal segments of threads, visible in ultra-thin sections, become shorter, presumably due to coiling. Nuclei at the diplotene phase contain single threads essentially similar to those seen at leptotene. As the oocyte enters the dictyate or resting phase, electron dense threads disappear from the nucleus. These observations suggest that the threads represent chromosomal ‘cores’. Nucleolus-like components persist throughout meiotic prophase, and at the diplotene phase regain the more complex form typical of oogonia. The cytoplasmic organelles become more numerous and complex as the oocyte approaches the dictyate phase. ‘Atretic divisions’ in oogonia are characterized by the persistence of long segments of nuclear membrane and the appearance of vesicles enveloped by a double membrane resembling the nuclear envelope. The dense masses of ‘chromatin’ (mitotic chromosomes) are more rounded than in normal cells at metaphase, and tend to coalesce. Spindle fibres have not been observed. Cytoplasmic organelles tend to increase in number and complexity. ‘ Z ’ cells (cells degenerating largely at the pachytene phase) show heavy ‘chromatin’ condensation around the tripartite ribbons. The major cytoplasmic changes consist in swelling of the endoplasmic reticulum, vacuolation of mitochondria and increase in incidence of multilamellar bodies. Atretic oocytes at the diplotene phase differ markedly from ‘ Z ’ cells in that ‘chromatin’ condensation around electron dense threads (single) is markedly less prominent. Cytoplasmic changes are similar to those of ‘ Z ’ cells, but also include a rise in the incidence of multivesicular and other complex bodies. All three types of degenerating cells are removed from the ovary by the phagocytic activity of neighbouring somatic cells.


1979 ◽  
Vol 150 (3) ◽  
pp. 703-708 ◽  
Author(s):  
Y Rikihisa ◽  
S Ito

Rickettsia tsutsugamushi (Gilliam strain) was serially propagated in BHK-21 cell cultures and incubated with guinea pig peritoneal polymorphonuclear leukocytes to study the ultrastructural features of rickettsial uptake and entry into the leukocytes. Significant numbers of rickettsiae were phagocytized selectively by these leukocytes within 30 min. About one-half of these rickettsiae remained sequestered in phagosomes but the other one-half were free from the phagosome and localized directly in the polymorphonuclear leukocyte cytoplasm. Various stages of rickettsial release from the phagosomes were observed. Once free within the polymorphonuclear leukocyte cytoplasm, the rickettsiae were preferentially localized in the glycogen-packed areas which are devoid of lysosomes and other cytoplasmic organelles. This study indicates that rickettsiae phagocytized by polymorphonuclear leukocytes can escape from the phagosome into the cytoplasm.


2018 ◽  
Vol 295 ◽  
pp. S243-S244
Author(s):  
S.H. Yoo ◽  
M.H. Jeong ◽  
E.H. Jang ◽  
Y.J. Jung ◽  
K.H. Chung

2018 ◽  
Vol 9 (10) ◽  
pp. 2690-2697 ◽  
Author(s):  
Jin-Sung Park ◽  
Il-Buem Lee ◽  
Hyeon-Min Moon ◽  
Jong-Hyeon Joo ◽  
Kyoung-Hoon Kim ◽  
...  

Despite recent remarkable advances in microscopic techniques, it still remains very challenging to directly observe the complex structure of cytoplasmic organelles in live cells without a fluorescent label.


2017 ◽  
Vol 34 (01) ◽  
pp. 023-030
Author(s):  
S. Senarat ◽  
J. Kettratad ◽  
W. Jiraungkoorskul

Abstract Introduction: Structure, ultrastructural features and degeneration of oogenesis were first investigated in female Rastrelliger brachysoma as new candidate species for aquaculture by transmission electron microscopy. Materials and Methods: Specimens were naturally collected during the breeding season from Samut Songkhram Province, Thailand. Results: The ultrastructure of female oogenesis was principally divided into five stages based on the nuclear characterization and cytoplasmic organelles; (i) oogonium; (ii) previtellogenic; (iii) lipid and cortical alveolar; (iv) early and (v) late vitellogenic stages. Initially, oogonium was present within cell nest in the epithelial compartment. Its cell was supported by prefollicular cells. The multiple nucleoli in previtellogenic stage, referring to primary growth stage were the first to appear and they were scattered around the peripheral of nuclear membrane with the increasing number of cytoplasmic organelles. Some microvilli of granulosa cell initially protruded into the vitelline envelope. A simple layer of flattened granulosa and theca cells was also observed. The lipid and cortical alveolar stage under secondary growth oocyte was accumulated with two inclusions; the lipid droplets and cortical alveoli in the ooplasm. Another characterization, the increasing of numerous microvilli was also detected in the vitelline envelope. Finally, in the vitellogenic stage, a massive uptake and processing of proteins into yolk platelets due to embedding of the numerous microvilli in the largest vitelline envelope was observed. Oocyte degeneration in R. brachysoma was novel found especially oogonial and previtellogenic stages. Conclusion: Five oogenic stages of this fish are found with the changing of the arrangement of nucleus, cytoplasmic organelles and follicular complex, which will be applied to further studies.


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