• Title/Summary/Keyword: Follicle cell

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Ultrastructural Study of the Process of Oocyte Degeneration and Function of the Follicle Cells in Female Spisula sachalinensis on the East Sea of Korea

  • Chung, Ee-Yung;Lee, Ki-Young;Lee, Jeong-Yong
    • The Korean Journal of Malacology
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    • v.24 no.1
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    • pp.33-40
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    • 2008
  • Ultastructural studies of oocyte degeneration and follicle cells in female Spisula sachalinensis are described for clams collected from Jumunjin, Gangwondo, Korea. The follicle cells playan integral role in vitellogenesis and oocyte degeneration by assimilating products originating from the degenerated oocytes (thus allowed the transfer of yolk precursors needed for vitellogenesis). The functions of the follicle cells include phagocytosis and intracellular digestion of products originating from oocyte degeneration. During the period of oocyte degeneration, follicle cells of this species probably have lysosomal systems for the breakdown and reabsorption of various phagosomes(phagolysosomes) in the cytoplasm for nutrient storage; this process has been observed in other bivalves.

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The Differential Distribution of Ganglioside GM3 in Atre tic Follicles During Follicular Development of Adult Rat Ovary (성숙한 난소의 난포 발달이 진행되는 동안 폐쇄난포에서의 Ganglioside GM3의 서로 다른 분포)

  • 추영국
    • The Korean Journal of Zoology
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    • v.39 no.4
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    • pp.410-418
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    • 1996
  • Gangilosides are ubiquitous membrane components in mammalian cells and are suggested to play essential roles in cellular phenomena such as cell-cell interadion, differentiation, and signal transduction. Rat ovary contained GM3 as major gangiloside. Nn order to study GM3 distribution in the atretic follicles and its possible changes during follicular development, frozen sections were stained with spedfic monocional antibodies against eleven gangilo-series gangliosides including GM3. In the atretic follicles, Glf3 was expressed in a spatlo-temporally different manner during foilicular development, but GM1 and other gangliosides were not immunohistochemicaily detected. in atretic follicle from primary follicle stage, GM3 was expressed in all the theca cells and some granulosa cells adjacent to oocyte. In atretic follicle from secondary follicle stage, GM3 were expressed in all theca cells and granulosa cells. in atretic follicles from developing Graaflan follicle stages, GM3 was similarly expressed as in secondary follicle stage.

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Morphological Changes of Radiation-Induced Atretic Follicles in Mouse Ovary

  • Kim Sung-In;Kwon O-Yu;You Kwan-Hee
    • Biomedical Science Letters
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    • v.12 no.2
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    • pp.105-112
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    • 2006
  • This study was undertaken to investigate the morphological changes between normal and atretic follicle after gamma irradiation and treatment of follicle stimulating hormone (FSH). The ovaries of each group of treated immature mice were prepared the paraffin sections after 0, 6, 12, and 24 hours (hrs) of those treatment. Hematoxylin-eosin (HE) stain, reticulin stain, and terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end labeling (TUNEL) immunohistochemical stain were performed on the each paraffin sections. As the results of HE staining, the condensed nuclei of oocytes were observed in the atretic primordial follicles, on the other hand the condensations of granulosa cell nuclei were prominent in the atretic primary, preantral, and antral follicles. Only the granulosa cells of atretic follicle were stained specifically with TUNEL staining but not stained in the theca cells, which suggested granulosa cells degenerated through apoptosis. In the reticulin staining, the basement membranes of atretic follicle which was stained weakly showed irregular structure and detachment from the follicles. The ratio of normal to atretic follicle in control and FSH treated group was about 33% but this ratio increased rapidly over 90% in the 6, 12, and 24 hrs group after the irradiation. It could be suggested that the gamma irradiation is the useful tool far the induction of follicle atresia and immunohistochemical staining methods are essential in the study of follicle atresia.

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Regulatory T Cells in B Cell Follicles

  • Chang, Jae-Hoon;Chung, Yeonseok
    • IMMUNE NETWORK
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    • v.14 no.5
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    • pp.227-236
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    • 2014
  • Understanding germinal center reactions is crucial not only for the design of effective vaccines against infectious agents and malignant cells but also for the development of therapeutic intervention for the treatment of antibody-mediated immune disorders. Recent advances in this field have revealed specialized subsets of T cells necessary for the control of B cell responses in the follicle. These cells include follicular regulatory T cells and Qa-1-restricted cluster of differentiation $(CD)8^+$ regulatory T cells. In this review, we discuss the current knowledge related to the role of regulatory T cells in the B cell follicle.

A study on the Gonad in Pieris rapae L. - III. Ultastructural study on the testis during the metamorphosis from prepupa to pupa (배추흰나비 (Pieris rapae L.)의 생식소에 관한 연구 - III. 전용에서 용으로 변태(變態)에 따른 정소(精巢)의 미세구조(微細構造)에 관하여)

  • Lee, K.O.;Kim, C.W.;Kim, W.K.
    • Applied Microscopy
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    • v.12 no.2
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    • pp.45-53
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    • 1982
  • Ultrastructural changes of the testis in Pieris rapae L. observed under the electron microscope during the metamorphosis from prepupa to pupa. The peritoneal sheath, epithelium of the follicle and cucticle have the maximum thickness at prepupa stage and afterthen gradually they began to degenerate. The epithelium of the follicle which formed by invagination of the peritoneal sheath is differently differentiationed from the peritoneal sheath and it is similar to the adult's from the pupa 2 days. The cell organelles begin to increase in the cytoplasm of the cyst cell enclosed the sperm bundles at pupa 3 hrs. The electron densed granules which observed in the peritoneal sheath and epithelium of the follicle at prepupa seem to be related with fusion of the testis.

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CHANGES OF THE CONCENTRATIONS OF STEROID HORMONES IN THE PORCINE FOLLICULAR FLUIDS ON ATRESIA (돼지여포의 퇴화과정 중 여포액 내 스테로이드 호르몬 양의 변화)

  • Lee, Young-Keun;Yoon, Yong-Dal
    • Clinical and Experimental Reproductive Medicine
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    • v.12 no.1
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    • pp.83-98
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    • 1985
  • In order to study the mechanism of follicular atresia, the follicles of the porcine ovary were isolated according to the presence or absence of the corpus luteum and their size, and then classified to the normal? or atretic?follicle on the morphological observation such as the transparency, the vascularization of follicle, the nuclear phase of oocyte, and the homogeneity of the granulosa cell layer. The viability of granulosa cells was examined. The concentrations of progesterone ($P_4$), testosterone (T), and estradiol-17 beta ($E_2$) in each follicular fluid were estimated by the radioimmunoassay. The viability of granulosa cells in the atretic follicle was much lower than that of the normal one. The concentration of each steroid hormone increased as the follicular size was increased, was not different in quantity between the normal- and the atretic follicle of which diameter was below 3mm, and were much higher in the atretic follicle than those in the normal one of which diameter was above 7mm. The ratio of the concentration of E2 to T in the large atretic follicle valued higher than that in the normal one, but smaller in the small and medium atretic follicle than that in the normal one. The present study suggests that the mechanism of atresia of the large follicle may be different from that of the small and the medium follicle and that the amount of steroid hormones regarded as the one of the criteria for the atretic follicles.

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Retrieval of Porcine Ovarian Follicles by Different Methods

  • Choi, Moon Hwan;Gong, Seung Pyo;Lim, Jeong Mook
    • Asian-Australasian Journal of Animal Sciences
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    • v.21 no.3
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    • pp.353-357
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    • 2008
  • A series of studies has been conducted to establish a base infrastructure for an ovarian follicle culture system in the porcine and this study was designed to develop an effective retrieval protocol of preantral follicles. Five different methods using collagenase type I (A) or IV (B, C1, C2 and C3), which employed different treatment durations and/or conditions, were employed and sliced ovarian tissue of prepubertal gilts was provided for the retrieval. A significant increase in total number of follicles retrieved was detected when collagenase IV (methods B or C) was used. In total, more ovarian follicles were retrieved by method B undertaking agitation and method C2 without the agitation than method C1 and C3, while the number of preantral follicles collected was the largest in method B. Neither incubation in 5% $CO_2$ in air atmosphere instead of the agitation nor increased duration of enzymatic treatment up to 120 minutes improved the efficiency of follicle retrieval. There were no differences in the number of follicles retrieved from intact ovaries and from used ovaries for oocyte collection. These results demonstrate the collagenase IV treatment with agitation is effective for retrieving porcine preantral follicles from the ovaries.

Oogenesis, Oocyte Degeneration and Sexual Maturation in Female Cyclina sinensis (Gmelin, 1971) (Bivalvia: Veneridae) in Korea

  • Chung, Ee-Yung;Koh, Chul-Hwan;Park, Gab-Man
    • Animal cells and systems
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    • v.11 no.2
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    • pp.191-198
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    • 2007
  • The ultrastructure of germ cells and follicle cells during oogenesis, oocyte degeneration, reproductive cycle, and first sexual maturity in female Cyclina sinensis were investigated for clams collected from Simpo, Jeollabuk-do, Korea, by cytological and histological observations. Vitellogenesis occured by way of endogeous autosynthesis and exogenous heterosynthesis: vitellogensis occurred through a process of autosynthesis, which involves a combined activities of the Golgi complex, mitochondria, and rough endoplasmic reticulum. The process of heterosynthesis involved endocytotic incorporation of extraovarian precursors into the basal region of the early vitellogenic oocytes prior to the formation of vitelline envelope. The follicle cells appear to play an integral role in vitellogenesis and oocyte degeneration, functioning in phagocytosis and digestion of products originating from the degenerated oocytes: these functions can permit the transfer of yolk precursors needed for vitellogenesis. Follicle cells might have a lysosomal system for breakdown and might also resorb phagosomes in the cytoplasm for nutrient storage during oocyte degeneration.

The Radioprotective Effect of Panax ginseng of the Hair Medullary Cell in Irradiated Mice (방사선 피폭 마우스의 털 수질세포에 대한 인삼의 방사선 방호효과)

  • 김성호;한동운
    • Journal of Ginseng Research
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    • v.20 no.2
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    • pp.149-153
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    • 1996
  • Studies were Performed to determine whether the water fraction of Panax ginseng Protected radiation damage to hair medullar cells of N:GP(s) mice after in vivo irradiation with $^{60}Co{\;}{\gamma}-rays$. The hair follicles in the middle of the growth cycle were analysed 3 days after 3 Gy irradiation for the changes in the number of cells in the forming medulla of the hair in the region just above the germinal matrix of the growing (anagen) hair follicle. The radioprotective effect of ginseng was compared with the irradiation control. The medullar cell count per unit length ($100{\;}\mu\textrm{m}$) of hair follicle was higher in the pretreated-groups of ginseng, both oral (2 mg/ml of drinking water, p<0.05) and intraperitoneal (0.3 mg/head, p<0.001) treatments, than the irradiation control. These data suggested that the water fraction of Panax ginseng may reduce cell damages on the body surface caused by ${\gamma}-rays$.

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The Immunohistochemical Changes of Skin during Hair Follicle Cycle after Depilation in Mice

  • Kim, Dae-Keun;Lee, Chang-Hyun
    • Biomedical Science Letters
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    • v.16 no.4
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    • pp.349-357
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    • 2010
  • We have examined the histological changes of skin during hair follicle growth after depilation in C57BL/6N mice. We first studied on histological changes of number of mast cells and thickness of skin during hair follicle growth periods (telogen, 1 day, 3 day, 5 day, 10 day, 14 day, 17 day and 21 day after depilation) by toluidine blue, Giemsa and H&E staining methods. We second studied immunoreactive density of cytokines and Brdu labeled cells in skin during hair follicle growth periods after depilation in C57BL/6N mice by immunohistochemical methods. The histological changes on skin thickness was increased from telogen to 14 day. The number of mast cells was decreased in 3,5 and 10 day and increased in 14, 17 and 20 day after depilation. Immunoreactive density of cytokines [protein kinase C-${\alpha}$ (PKC-${\alpha}$), c-kit, and vascular endothelial growth factor (VEGF)] in 1, 3, 5, 10, and 14 day after depilation was mildly stained in bulge and cutaneous trunci m., but immunoreactive density of cytokines in 17 and 21 day was heavily stained in epidermis, bulge, outer root sheath (ORS), inner root sheath (IRS) and cutaneous trunci m.. Immunoreactive density of Brdu labeled cells in skin in 1 and 3 day was heavily stained in bulge, epidermis and connective tissue under the cutaneous trunci m.. In all periods, immunoreactive density of Brdu labeled cells in skin was heavily stained in bulge, subcutaneous tissue, cutaneous trunci m, ORS and IRS. These experiments suggest that histological changes related to hair follicle growth elevated mast cell counts, skin thickness and epidermis thickness and heavily stained immunoreactive density of cytokines and Brdu labeled cutaneous trunci m. and connective tissue under the cutaneous trunci m. after depilation in C57BL/6N mice.