• 제목/요약/키워드: induced maturation

검색결과 241건 처리시간 0.03초

Prolonged Exposure to Lipopolysaccharide Induces NLRP3-Independent Maturation and Secretion of Interleukin (IL)-1β in Macrophages

  • Hong, Sujeong;Yu, Je-Wook
    • Journal of Microbiology and Biotechnology
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    • 제28권1호
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    • pp.115-121
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    • 2018
  • Upon sensing of microbial infections or endogenous danger signals in macrophages, inflammasome signaling plays a significant role in triggering inflammatory responses via producing interleukin (IL)-$1{\beta}$. Recent studies revealed that active caspase-1, a product of the inflammasome complex, causes maturation of inactive pro-IL-$1{\beta}$ into the active form. However, the underlying mechanism by which this leaderless cytokine is secreted into the extracellular space remains to be elucidated. In this study, we demonstrated that prolonged lipopolysaccharide (LPS) treatment to macrophages could trigger the unexpected maturation and extracellular release of IL-$1{\beta}$ through a nucleotide-binding oligomerization domain-like receptor family, pyrin domain-containing 3 (NLRP3)-independent manner. Short-term treatment (less than 6 h) of LPS induced robust production of the IL-$1{\beta}$ precursor form inside cells but did not promote the maturation and secretion of IL-$1{\beta}$ in bone marrow-derived macrophages or peritoneal macrophages. Instead, prolonged LPS treatment (more than 12 h) led to a significant release of matured IL-$1{\beta}$ with no robust indication of caspase-1 activation. Intriguingly, this LPS-triggered secretion of IL-$1{\beta}$ was also observed in NLRP3-deficient macrophages. In addition, this unexpected IL-$1{\beta}$ release was only partially impaired by a caspase-1 and NLRP3 inflammasome inhibitor. Collectively, our results propose that prolonged exposure to LPS is able to drive the maturation and secretion of IL-$1{\beta}$ in an NLRP3 inflammasome-independent manner.

Oocyte maturation under a biophoton generator improves preimplantation development of pig embryos derived by parthenogenesis and somatic cell nuclear transfer

  • Lee, DJoohyeong;Shin, Hyeji;Lee, Wonyou;Lee, Seung Tae;Lee, Geun-Shik;Hyun, Sang-Hwan;Lee, Eunsong
    • 대한수의학회지
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    • 제57권2호
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    • pp.89-95
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    • 2017
  • This study was conducted to determine the effects of biophoton treatment during in vitro maturation (IVM) and/or in vitro culture (IVC) on oocyte maturation and embryonic development in pigs. An apparatus capable of generating homogeneous biophoton energy emissions was placed in an incubator. Initially, immature pig oocytes were matured in the biophoton-equipped incubator in medium 199 supplemented with cysteine, epidermal growth factor, insulin, and gonadotrophic hormones for 22 h, after which they were matured in hormone-free medium for an additional 22 hr. Next, IVM oocytes were induced for parthenogenesis (PA) or provided as cytoplasts for somatic cell nuclear transfer (SCNT). Treatment of oocytes with biophoton energy during IVM did not improve cumulus cell expansion, nuclear maturation, intraoocyte glutathione content, or mitochondrial distribution of oocytes. However, biophoton-treated oocytes showed higher (p < 0.05) blastocyst formation after PA than that in untreated oocytes (50.7% vs. 42.7%). In an additional experiment, SCNT embryos produced from biophoton-treated oocytes showed a greater (p < 0.05) number of cells in blastocysts (52.6 vs. 43.9) than that in untreated oocytes. Taken together, our results demonstrate that biophoton treatment during IVM improves developmental competence of PA- and SCNT-derived embryos.

미세조류 3종에 따른 피조개 Scapharca broughtonii의 생식소 발달과 성숙 (Effect of Three Microalgal Species on Gonadal Development and Sex Maturation of Ark Shell, Scapharca broughtonii)

  • 민병희;김병학;김성연;신윤경;허성범
    • 한국패류학회지
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    • 제27권2호
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    • pp.143-148
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    • 2011
  • 연구는 양질의 피조개 수정란 확보와 안정적 종묘생산을 위하여 피조개 모패의 먹이생물로 미세조류 3종 (Isochrysis galbana, Tetraselmis tetrathele, Phaeodactylum tricornutum) 을 단독 또는 혼합 공급하여 먹이생물에 따른 피조개 모패의 비만도, 생식소발달, 성숙유도율 및 생존율을 조사하였다. 사육 45일 경과 후 피조개 모패의 완숙기 출현율, 성숙유도율 및 생존율은 3종의 미세조류를 혼합 공급하거나 T. tetrathele를 단독공급한 실험구에서 가장 높았다.

In vitro maturation of human pluripotent stem cell-derived cardiomyocyte: A promising approach for cell therapy

  • Park, Yun-Gwi;Son, Yeo-Jin;Moon, Sung-Hwan;Park, Soon-Jung
    • 한국동물생명공학회지
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    • 제37권2호
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    • pp.67-79
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    • 2022
  • Currently, there is no treatment to reverse or cure heart failure caused by ischemic heart disease and myocardial infarction despite the remarkable advances in modern medicine. In addition, there is a lack of evidence regarding the existence of stem cells involved in the proliferation and regeneration of cardiomyocytes in adult hearts. As an alternative solution to overcome this problem, protocols for differentiating human pluripotent stem cell (hPSC) into cardiomyocyte have been established, which further led to the development of cell therapy in major leading countries in this field. Recently, clinical studies have confirmed the safety of hPSC-derived cardiac progenitor cells (CPCs). Although several institutions have shown progress in their research on cell therapy using hPSC-derived cardiomyocytes, the functions of cardiomyocytes used for transplantation remain to be those of immature cardiomyocytes, which poses a risk of graft-induced arrhythmias in the early stage of transplantation. Over the last decade, research aimed at achieving maturation of immature cardiomyocytes, showing same characteristics as those of mature cardiomyocytes, has been actively conducted using various approaches at leading research institutes worldwide. However, challenges remain in technological development for effective generation of mature cardiomyocytes with the same properties as those present in the adult hearts. Therefore, in this review, we provide an overview of the technological development status for maturation methods of hPSC-derived cardiomyocytes and present a direction for future development of maturation techniques.

한국산개구리(북장산개구리와 참개구리) 난자의 생체외 배양에 의한 성숙유도에 관하여 (Studies on the Induction of Oocyte Maturation of Korean Frogs(R. dybowskii and R. niqromaculata) in vitro.)

  • 권혁방;조장현;최충길
    • 한국동물학회지
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    • 제31권2호
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    • pp.87-94
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    • 1988
  • 전라남도 일대에서 서식하는 북방상개구리(R. dybowskii)와 참개구리(R. nigromaculara)를 채집하는 생체외배양에 의한 여포난자의 성숙을 유도하였다. 북방산개구리의 여포난자는 배양액(amphibian Ringer's soluion AR)에 첨가한 progesterone, 0.1 $\mu$g/2 ml에 의해 난자의 성숙(핵붕괴)이 유도 되었으며 참개구리의 난자는 1 $\mu$g/2 ml (frog pituitary homogenate FPH)을 얻어서 그 효과를 조사해본 결과 북방산개구리에서는 0.01 pituitary equivalent/2 ml에서, 참개구리는 0.1 pit equiv./2 ml에서부터 여포난자의 성숙이 일어났다. 난자의 성숙에 요하는 시간은 두 개구리에서 모두 9-15시간이었으며 호르몬에 대한 반응성, 성숙기간 등은 개구리 재료로 가장 많이 사용되는 법개구리(R. pipiens)와 거의 일치하였다. 특이하게 2개월 이후에 사용한 북방산개구리의 여포난자는 호르몬의 도움없이도 성숙이 일어났으며 성숙기간도 3시간으로 매우 빨라졌다. 난소조각을 배양했을 때 자발적으로 성숙을 일으키는 여포들은 자발적인 배란까지도 일으키는 것을 발견하였다.

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생쥐 난자성숙에 미치는 $Ca^{++}$ Ionophore와 $Ca^{++}$ Channel Blocker의 영향 (Effect of $Ca^{++}$ Ionophore and $Ca^{++}$-Channel Blocker on the Mouse Oocyte Maturation)

  • 배인하;김현숙;김문규
    • Clinical and Experimental Reproductive Medicine
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    • 제19권2호
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    • pp.105-116
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    • 1992
  • The present study was examined to clarify the role of calcium ion as a factor for the maturation of mouse oocytes. Follicles and cumulus-enclosed oocytes were isolated with two sharp needles under a stereomicroscope from female mouse (ICR) ovaries which were treated PMSG 5 IU 45-46 hours previously. Isolated follicles and cumulus-enclosed oocytes were cultured for 14-16 hours in an organ culture system at $37^{\circ}C$, 5% $CO_2$ in air and 100% humudified in incubator. MHBS was the basic medium used from which A23187, verapamil, $NiCl_{2.}$ $6H_2O$ and $LaCl_{3.}$ $7H_2O$ were added depending on the experimental groups. In follicle- or cumulus-enclosed oocytes wre cultured in these differently treated media. Following results were obtained from the present study. 1. The calcium ionophore A23187 directly or indirectly seems to stimulate GVBD of follicle-enclosed mouse oocytes. Increasing concentration of ionophore A23187 1ed to an increase in oocytes degeneration from the cumulus-enclosed mouse oocytes. 2. The organic $Ca^{++}$ channel blocker, verapamil does not induce GVBD of follicle-enclosed mouse oocytes. Specially, higher dose of 1 mM verapamil induced GVBD of follicle-enclosed mouse oocytes. However, cytoplasm of GVBD oocytes in 1 mM verapamil treated groups appeared shrunk. In the cumulus-enclosed oocytes, polar body formation was reduced in verapamil treated groups and degeneration increased. Verapamil inhibit oocyte maturation (polar body formation). 3. The $Ca^{++}$ inhibitor, Nickel ($NiCl_{2.}$ $6H_2O$) inhibits maturation of the follicle-enclosed oocytes. In the cumulus-enclosed oocytes the progression to MII (PB formation) was reduced and degeneration of mouse oocytes increased as the concentration of $Ni^{++}$ increase. The results indicates that nickel act as an inhibitor of calcium. 4. The $Ca^{++}$ inhibitors, Lanthanum ($LaCl_{3.}$ $7H_2O$) has shown different effect from that of nickel. In follicle-enclosed oocytes, 0.01mM lanthanum induced maturation of mouse oocytes. Polar body formation was reduced in the cumulus-enclosed oocytes all lanthanum treated group.

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