• 제목/요약/키워드: cytoplasm

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북방대합 (Spisula sachalinensis) 생식세포의 미세구조 (Ultrastructure of Germ Cell during the Gametogenesis in Surf Clam, Spisula sachalinensis)

  • 이정용;장윤정;장영진
    • 한국수산과학회지
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    • 제36권2호
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    • pp.157-162
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    • 2003
  • Ultrastructure of germ cell during gametogenesis of surf clam, Spisula sachalinensis were investigated by electron microscopic observations. Oogonia are oval in shape and 5-6 ${\mu}m$ in diameter. They contain a large nucleus and have several mitochondria in the cytoplasm. Vitellogenic oocytes grew attached by a stalk to the germinal epithelium in the ovarian sac and their cytoplasm contained many yolk granules, lipid granules and mitochondria. Mature oocytes measuring 50-60 ${\mu}m$ in diameter have a nucleus containing an electron dense nucleolus, and a lots of yolk granules, lipid granules, mitochondria, rough endoplasmic reticulum and cortical granules were present in the cytoplasm. The surface of the plasma membrane in mature oocytes was formed of microvilli approximately 1.5 ${\mu}m$ long and enveloped in the vitelline layer. Spematogonia are oval in shape and about 5 ${\mu}m$ in diameter. Sprmatogonia develop into spermatocyte, spermatid and spermatozoon. The spermatozoon consisted of the head, midpiece and tail. The sperm head with diameter of about 1.5 ${\mu}m$ was ovoid, and contained the nucleus which consisted of acrosome. The four mitochondria encircled the centrosome in midpiece. The flagellum measuring about 40 ${\mu}m$ long had the classical 9+2 axoneme structure.

메뚜기 (Euprepocnemis shirakii) 성충의 혈구유형 (Hemocyte Types in Adult Grasshpper, Euprepocnemis shirakii Bolivar)

  • 장병수;한성식;여성문
    • Applied Microscopy
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    • 제24권2호
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    • pp.93-104
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    • 1994
  • Six types of hemocytes were identified in adult grasshopper, Euprepocnemis shirakii Bolivar. The morphological and ultrastructural characteristics of these cells were characterized by phase contrast, scanning and transmission electron microscope. The prohemocytes are small and spherical cells with large nucleus. The plasmatocytes are spindle shaped or polymorphic cells which show numerous cytoplasmic processes on the cell surface and they have lysosomes and vesicles that may be involved in phagocytic function. Especially, multivesicular bodies are observed in the polymorphic cells. The granulocytes I are spherical shaped cells. They are characterized by a number of electron dense granules measuring $0.2-0.3{\mu}m$ in average diameter and marginal band of microtubules which are always in close proximity to the cell membrane. The granulocytes II are oval or spindle-shaped cells. They contain large electron dense granules measuring $0.5-0.8{\mu}m$ in average diameter. Their cytoplasm is filled with numerous granules. The spherulocytes contain large amounts of spherules that most of their cytoplasm. Spherules filled with fine granules or flocculent materials. The oenocytoids are large spherical cells with few cytoplasmic organelles. Their cytoplasm contains peculiar aspect of motochondria and numerous polyrobosome.

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자기기생하는 실새삼(Cuscuta australis)에서 세포 화합성에 관한 미세구조 연구 (Ultrastructural Study on the Cellular Compatibility in Self-Parasiting Cuscuta australis)

  • 이규배
    • Journal of Plant Biology
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    • 제36권3호
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    • pp.285-292
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    • 1993
  • Cellular compatibility in the self-parasitism of Cuscuta australis R. Brown was studied at the ultrastructural level. The front cells of the haustorium penetrated the host stems independently grew within the host tissues and transformed into elongate, filamentous hyphae. Each hyphal cells contained a large nucleus and dense cytoplasm with abundant cell organelles. Multilamellar structures were contained in the cytoplasm and cell walls of the penetrating hyphal cells. When the hyphal cells did not yet invade the host cells, the middle lamella and the fused cellulosic cell walls of the two partners at the host-parasite interface were preserved well. As the invasion of the parasitic hyphal cells progressed, however, the middle lamella was not found at the interface and the host cell walls and plasma membranes were partially broken down. A hyphal cell penetrated deeply into the host cell had a more darkly stained cytoplasm with numerous of cell organelles. In the host cells attacked by the hyphal cells the limiting membranes of plastids were broken down and several vesicles were arrayed near the cell walls. No plasmodesmatal connections between the host and parasite cell walls were found; however, half-plasmodesmata were observed frequently on the side of the hyphal cell walls. These results suggested that the compatibility response in the self-parasitism of Cuscuta was expressed by cell walls, not by plasmodesmata, between the host and the parasite cells.

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근세포 분화에 관한 연구 계배의 Myoblasts에 있어서 Protein Kinase C (PKC)의 인 산화작용과 Down Regulation (Studies on the Differentiation of Skeletal Muscle Cells in uitro : The Phosphorylation and Down Regulation of Protein Kinase C in Myoblasts of Chick Embryos)

  • 문현근;최원철
    • 한국동물학회지
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    • 제35권2호
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    • pp.161-172
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    • 1992
  • In the short-term treahent of 12-0-tetradecanoylphorbol-13-acetate (TPA) or platelet-derived growth factor (PDGF), the'Wh and PDGF induced the Protein Kinase C (PKC) activation and migration from the cytoplasm to the peripheral nulcear membrane. And the activated PKC which was directly or indirectly stimulated by TPA or PDGF Phosphorylated many kinds of PKC's targeting proteins and induces various biological responses. Especially, the cytoplasmic PKC was phosphorylated within 1 hr and 10 min by TPA-and PDGF-treahent respectivelv. In the long-term treatment of TPA or PDGF, both of them induced the down-regulation and translocation of PKC in the mvoblasts. The down-regulation of PKC isozyrnes, the pattern of PKC I and ll was similar to the PKC 111 isozpnes in the cytoplasm. But in the nucleolus, the TPA did not induce and down-regulation or the inhibition of the immunoreactivity of PKC III antibody. This investigation indicates that each isozvmes of PKC mal be performed the different effects to the down-regulation of the cytoplasm or nucleolus. And douvn-regulated myoblasts contained low immunoreactivity of PKC antibodies.

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HSV-1 ICP27 induces apoptosis by promoting Bax translocation to mitochondria through interacting with 14-3-3θ

  • Kim, Ji Ae;Kim, Jin Chul;Min, Jung Sun;Kang, Inho;Oh, Jeongho;Ahn, Jeong Keun
    • BMB Reports
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    • 제50권5호
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    • pp.257-262
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    • 2017
  • The subcellular localization of Bax plays a crucial role during apoptosis. In response to apoptotic stimuli, Bax translocates from the cytoplasm to the mitochondria, where it promotes the release of cytochrome c to the cytoplasm. In cells infected with HSV-1, apoptosis is triggered or blocked by diverse mechanisms. In this study, we demonstrate how HSV-1 ICP27 induces apoptosis and modulates mitochondrial membrane potential in HEK 293T cells. We found that ICP27 interacts with $14-3-3{\theta}$ which sequesters Bax to the cytoplasm. In addition, ICP27 promotes the translocation of Bax to the mitochondria by inhibiting the interaction between $14-3-3{\theta}$ and Bax. Our findings may provide a novel apoptotic regulatory pathway induced by ICP27 during HSV-1 infection.

Ultrastructural studies of vitellogenesis in oocytes and follicle cells during oogenesis in female Protothaca (Notochione) jedoensis (Bivalvia: Veneridae)

  • Kang, Hee-Woong;Choi, Ki-Ho;Jun, Je-Cheon;Lee, Ki-Young;Park, Kwan-Ha
    • Animal cells and systems
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    • 제14권4호
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    • pp.343-349
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    • 2010
  • Ultrastructural studies of vitellogenesis in oocytes and follicle cells during oogenesis in female Protothaca (Notochione) jedoensis were investigated by histological and transmission electron microscope observations. In early vitellogenic oocytes, combined activities of the Golgi complex, mitochondria and rough endoplasmic reticulum in the cytoplasm are associated with autosynthetic vitellogenesis. Furthermore, at this time, many coated vesicles at the basal region of the oolemma of the oocyte lead to the formation of vesicles through endocytosis in the cytoplasm. Through the formation of the coated pits on oolemma during vitellogenesis, the uptake of extrafollicular precursors (nutritive materials) occurs in coated vesicles by endocytosis. Therefore, it is assumed that these exogenous materials are involved in heterosynthetic vitellogenesis. During late oogenesis, exogenous yolk precursors (yolk granules), lipid droplets and proteinaceous yolk granules are present in the cytoplasm of late vitellogenic oocytes. In mature oocytes, small yolk granules appear intermingled and form large mature yolk granules. Thus, two processes of vitellogenesis occur in oocytes by way of endogenous autosynthesis and exogenous heterosynthesis. The follicle cells attached to the oocytes appear to play an integral role in vitellogenesis in this study.

Ultrastructural Study on Induced Resistance of Cucumber Plants against Sphaerotheca fuliginea by Oligochitosan

  • Ma, Qing;Zhao, Xiao-Ming;Sun, Hui;Shang, Hong-Sheng
    • The Plant Pathology Journal
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    • 제27권1호
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    • pp.8-13
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    • 2011
  • The induced resistance of cucumber leaves treated with oligochitosan to the infection of the cucumber powdery mildew, Sphaerotheca fuliginea, was investigated using transmission electron microscopy. The results showed that when the plants were treated with oligochitosan and challenged with inoculum, a significant decrease of the disease occurred. The mycelial development in the treated leaves was markedly inhibited. The cytoplasm of the powdery mildew mycelium was aggregated, with its organelles disintegrated and the cytoplasm collapsed. The protoplasm in haustoria became electron-dense. Haustoria became malformed, their organelles disintegrated, the hausterial wall thickened and eventually the whole complex necrotized. The host cells produced defence structures and materials associated with infection and a hypersensitive response. The host cell wall was thickened and deeply stained; several layers of papilla structure were produced under the cell wall; dark materials were deposited between the cell wall and plasmalemma; extrahaustorial plasmalemma was deeply stained and extrahaustorial matrix appositions had large deposits of electron-dense material; the cytoplasm was disordered, host organelles disintegrated and eventually the whole host cell disintegrated and necrotized.

먹물버섯의 자가분해 과정에 대한 미세구조 연구 (Ultrastructural Studies on the Autolysis of Coprinellus congregatus)

  • 최형태;조정원
    • 미생물학회지
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    • 제41권4호
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    • pp.312-315
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    • 2005
  • 먹물버섯의 하나인 Coprinellus congregatus에서는 자실체가 성숙된 후 곧 자가분해되어 먹물로 전환된다. 이 자가분해 과정과 관련된 가수분재 효소의 역할을 이해하기 위한 첫 단계로서, 자가분해과정과 연관된 미세구조의 변화를 전자현미경으로 조사하였다. 자실체의 성숙과정에서 자실층과 자실하층에 존재하는 모든 세포질은 새로운 포자의 형성을 위하여 포자로 이동되는 것으로 보인다. 조직 내의 세포질의 고갈과 포자의 완성은 조직 내의 세포벽의 분해를 야기하는 것으로 보이며, 자실층과 자실하층의 세포벽은 동시적으로 분해 되는 것으로 생각된다. 본 연구는 먹물버섯의 자가분해가 세포질의 분해가 아닌 세포벽의 분해과정에 의한 것임을 보여 주었으며, chitin 분해효소와 같은 가수분해 효소의 중요성을 제시하였다.

Fi'bricola seoulenis 조직융해구의 투사전자현미경 소견 (Transmission electron microscopic findings of the tribocytic organ of Fibricola seoulensis)

  • 송호복
    • Parasites, Hosts and Diseases
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    • 제31권4호
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    • pp.315-320
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    • 1993
  • Fibricola seoulensis 조직융해구(tribocytic organ)의 미세구조를 알기 위하여, 전자현미경으로 관찰하였다. 조직응해구의 표피에서 미세응모가 관찰되었다. 조직융해구에는 3가지 형태의 세포들이 관찰되는 데, 첫째는 방추형이고, 핵 및 원형질이 전자밀도가 낮고, 원형질내 직경 $0.1-0.2{\;}\mu\textrm{m}$의 과립이 소수 관찰된다 둘째는 방추형이고, 핵 및 원형질이 전자밀도가 높고, 직경 $0.1-0.2{\;}\mu\textrm{m}$의 미립자로 구성된 과립을 포함한다 셋째는 원형질이 전자밀도가 높고, 직경 $0.3-1.2{\;}\mu\textrm{m}$의 과립을 다수 포함한다. 위의 세포들 중, 첫째와 둘째 세포는 표피세포로, 셋째는 조직응해구의 특 이 분비세포로 추정한다. 이것은 조직융해구의 분비 기능을 설명할 수 있는 또 다른 소견이라고 할 수 있다.

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Intron retention decreases METTL3 expression by inhibiting mRNA export to the cytoplasm

  • Sangsoo Lee;Haesoo Jung;Sunkyung Choi;Namjoon Cho;Eun-Mi Kim;Kee Kwang Kim
    • BMB Reports
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    • 제56권9호
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    • pp.514-519
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    • 2023
  • Methyltransferase-like 3 (METTL3), a key component of the m6A methyltransferase complex, regulates the splicing, nuclear transport, stability, and translation of its target genes. However, the mechanism underlying the regulation of METTL3 expression by alternative splicing (AS) remains unknown. We analyzed the expression pattern of METTL3 after AS in human tissues and confirmed the expression of an isoform retaining introns 8 and 9 (METTL3-IR). We confirmed the different intracellular localizations of METTL3-IR and METTL3 proteins using immunofluorescence microscopy. Furthermore, the endogenous expression of METTL3-IR at the protein level was different from that at the mRNA level. We found that 3'-UTR generation by intron retention (IR) inhibited the export of METTL3-IR mRNA to the cytoplasm, which in turn suppressed protein expression. To the best of our knowledge, this is the first study to confirm the regulation of METTL3 gene expression by AS, providing evidence that the suppression of METTL3 protein expression by IR is an integral part of the mechanism by which 3'-UTR generation regulates protein expression via inhibition of RNA export to the cytoplasm.