• Title/Summary/Keyword: Germ cell

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Expression of Murine Asb-9 During Mouse Spermatogenesis

  • Lee, Man Ryul;Kim, Soo Kyoung;Kim, Jong Soo;Rhim, Si Youn;Kim, Kye-Seong
    • Molecules and Cells
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    • v.26 no.6
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    • pp.621-624
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    • 2008
  • We previously showed that Asb-4 and Asb-17 is uniquely expressed in developing male germ cells. A recent report showed that Asb-9 is specifically expressed in the kidney and testes; however, detailed expression patterns in developing germ cells have not been shown. Northern blot analysis in various tissues demonstrated that mAsb-9 was strongly expressed in the testes. Expression analysis by RT-PCR and Northern blot in developing mouse testes indicates that mAsb-9 is expressed from the fourth week after birth to adulthood, with the highest expression in round spermatids. Expression sites were further localized by in situ hybridization in the testes. Pachytene spermatocytes and spermatids expressed mAsb-9 but spermatogonia and generated spermatozoa did not. This study reveals that mAsb-9 could be a specific marker of active spermatogenesis and would be useful for studies of male germ cell development.

Effects of intravenous multiple busulfan injection on suppression of endogenous spermatogenesis in recipient stallion testes

  • Jung, Heejun;Yoon, Minjung
    • Journal of Animal Science and Technology
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    • v.63 no.5
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    • pp.1194-1203
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    • 2021
  • Preparation of recipient stallions is critical step to produce donor spermatogonial stem cell (SSC) derived sperm using transplantation technique. This study was conducted to evaluate the effects of intravenous busulfan infusion on germ cell depletion, semen production, and libido in stallions. Six Thoroughbred stallions were separated into two treatment groups: 1) a multiple low-dose (2.5 mg/kg bw for the first 4 weeks and 5 mg/kg bw for the 5th week); and 2) control group treated with PBS. Testicular samples were obtained at 11 weeks and classified into three different patterns of spermatogenesis, such as normal, Sertoli cell only, and destroyed. Semen collection and libido experiments were performed 1 week before treatment, and 4 and 8 weeks after treatment. For the sperm analysis, total spermatozoa and motility were measured using a light microscope with a motility analyzing system. In the multiple low-dose group, the numbers of tubules categorized as Sertoli cell only were significantly higher than those in the control as well as the total population and total/progressive motility of sperm were significantly decreased 8 weeks after the start of the treatment. The sperm production and motility in the multiple low-dose group appears to be reduced, while libido was maintained. In conclusion, multiple administration of 2.5 mg/kg bw busulfan depletes endogenous germ cells in the stallion recipients for SSC transplantation.

Utilization of Primordial Germ Cell(PGC) as Transferor of Avian Genetic Materials (가금의 유전물질전달체로서의 원시생식세포의 이용)

  • 여정수
    • Korean Journal of Animal Reproduction
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    • v.12 no.1
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    • pp.11-14
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    • 1988
  • Utilizatin of primordial germ cell(PGC) as transferor of genetic materials is great potential in manipulating genes to promote genetic performances in chicken. This study explored that PGCs from early embryos as vehicle for molecular breeding strategles were isolated, these chromosomally marked donor PGCs were transplanted to germinal crescent of host embryos, and genetic materials of donor PGC were identified at the proliferative stage in host gonads.

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Delayed diagnosis of intramedullary spinal cord germinoma

  • Kim, Haelim;Lee, Eung-Joon;Sung, Jung-Joon
    • Annals of Clinical Neurophysiology
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    • v.22 no.2
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    • pp.109-111
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    • 2020
  • Germ-cell tumors (GCTs) are common in the central nervous system. GCTs are highly sensitive to radiotherapy and chemotherapy and can be cured without radical surgery. However, this tumor produces nonspecific imaging findings, and its rarity can make diagnosis challenging. Here we report a case in which the first diagnosis was uncertain and follow-up imaging revealed intramedullary germinoma. The patient underwent chemotherapy and radiotherapy after the diagnosis.

Pre-Infection Behavior of the Pitch Canker Fungus Fusarium circinatum on Pine Stems

  • Thoungchaleun, Vilakon;Kim, Ki-Woo;Lee, Don-Koo;Kim, Chang-Soo;Park, Eun-Woo
    • The Plant Pathology Journal
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    • v.24 no.2
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    • pp.112-117
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    • 2008
  • Pre-infection behavior of Fusarium circinatum on stems of pine species was investigated with scanning electron microscopy. Two-year-old stems of Pinus densiflora and p. rigida were inoculated with the fungal conidial suspension and subjected to $25^{\circ}C$ for up to 16 hr. Most microconidia germinated 12 hr after inoculation on pine stems. Conidia produced germ tubes from either one or both ends of microconidia. Germ tubes grew over the stem surface and appeared to enter host tissues through natural openings on pine stems. Surface cracks in the cork were entrance sites of germ tubes of F. circinatum. In addition, host cell wall cracks were often found at the tip of germ tubes. The cuticle appeared to be eroded either at the tip of germ tubes or around germlings. Germ tubes also produced appressoria-like structures, exhibiting swollen tips of germ tubes on the stem surface. There seems to be no significant differences in the pre-infection behavior of F. circinatum on stems between the two pine species.

Apoptosis of Germ Cells after Vasectomy in Rats (수컷 랫드에서 졍관절제술에 의한 생식세포의 Apoptosis)

  • Choi, Jong-yun;Cho, Sung-whan;Ryu, Si-yoon;Jee, Young-heun;Lee, Geun-jwa;Son, Hwa-young
    • Korean Journal of Veterinary Research
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    • v.43 no.3
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    • pp.485-492
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    • 2003
  • The pathological mechanism of impaired spermatogenesis after vasectomy has not been completely investigated. In this study, we examined pathological changes of the testis and the Fas-Fas ligand (FasL) mediated signaling pathway in apoptotic germ cell death after vasectomy in rats. Ten-weeks old Sprague-Dawley rats were underwent bilateral vasectomy and sacrificed after 1 day, 2 days, 3 days, 5 days, 1 week, 2 weeks, and 4 weeks of surgery and the testes were removed. Histopathological evaluation of spermatogenesis was performed by hematoxylin-eosin and periodic acid-Schiff-hematoxylin staining. To elucidate the pathophysiology of seminiferous tubule damage, terminal dUTP nick end labeling staining, electrophoresis assay of DNA fragmentation, and Western blotting analysis for Fas-FasL were performed. Relative weights of testes were decreased from 5 days after vasectomy. Germ cell degeneration were first found in the spermatogonia and spermatocytes at stages I-VI, and XII-XIV seminiferous tubules. Mean incidence of apoptotic germ cells after vasectomy progressively increased to peak in 5 days, and then gradually decreased to the control levels in 2 weeks after vasectomy. The expression of Fas-FasL reached maximum level at 5 days after vasectomy and then declined. In conclusion, impaired spermatogenesis after vasectomy associated with an increase in germ cell apoptasis, which is partly mediated by the activation of Fas-FasL.

PGC-Enriched miRNAs Control Germ Cell Development

  • Bhin, Jinhyuk;Jeong, Hoe-Su;Kim, Jong Soo;Shin, Jeong Oh;Hong, Ki Sung;Jung, Han-Sung;Kim, Changhoon;Hwang, Daehee;Kim, Kye-Seong
    • Molecules and Cells
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    • v.38 no.10
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    • pp.895-903
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    • 2015
  • Non-coding microRNAs (miRNAs) regulate the translation of target messenger RNAs (mRNAs) involved in the growth and development of a variety of cells, including primordial germ cells (PGCs) which play an essential role in germ cell development. However, the target mRNAs and the regulatory networks influenced by miRNAs in PGCs remain unclear. Here, we demonstrate a novel miRNAs control PGC development through targeting mRNAs involved in various cellular pathways. We reveal the PGC-enriched expression patterns of nine miRNAs, including miR-10b, -18a, -93, -106b, -126-3p, -127, -181a, -181b, and -301, using miRNA expression analysis along with mRNA microarray analysis in PGCs, embryonic gonads, and postnatal testes. These miRNAs are highly expressed in PGCs, as demonstrated by Northern blotting, miRNA in situ hybridization assay, and miRNA qPCR analysis. This integrative study utilizing mRNA microarray analysis and miRNA target prediction demonstrates the regulatory networks through which these miRNAs regulate their potential target genes during PGC development. The elucidated networks of miRNAs disclose a coordinated molecular mechanism by which these miRNAs regulate distinct cellular pathways in PGCs that determine germ cell development.