http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Two new species of phoretic mites on ground beetle (Coleoptera: Carabidae)
Jaeseok Oh,Seunghwan Lee 한국응용곤충학회 2023 한국응용곤충학회 학술대회논문집 Vol.2023 No.10
Beetles are one of the most effective transportation for phoretic chelicerata. They use various methods to attach themselves to their hosts, such as developing ventral sucker plates, grasping with their claws and chelicerae, or hiding beneath the elytra. Recently, we discovered new species of two genera: Antennoseius (Mesostigmata: Blattisociidae) and Gaeolaelaps (Mesostigmata: Laelapidae) which are hiding under the elytra of Carabidae hosts. In this study, digital images of the beetles, and mites, along with brief diagnostic information and line-drawing plates will be provided.
Oh, Yoon Sin,Lee, Youn-Jung,Kang, Yup,Han, Jaeseok,Lim, Oh-Kyung,Jun, Hee-Sook Journal of Endocrinology, Ltd. [etc.] 2013 The Journal of endocrinology Vol.216 No.3
<P>Prolonged exposure to high glucose (HG) and palmitate (PA) results in increased ER stress and subsequently induces β-cell apoptosis. Exendin-4, a glucagon-like peptide-1 agonist, is known to protect β cells from toxicity induced by cytokines, HG, or fatty acids by reducing ER stress. However, the detailed molecular mechanisms for this protective effect are still not known. In this study, we investigated the role of exendin-4 in the inhibition of glucolipotoxicity-induced ER stress and β-cell apoptosis. Exendin-4 treatment protected INS-1 β cells from apoptosis in response to HG/PA (25 mM glucose+400 μM PA). HG/PA treatment increased cleaved caspase-3 and induced ER stress maker proteins such as PERK (EIF2AK3), ATF6, and phosphorylated forms of PERK, eIF2α, IRE1α (ERN1), and JNK (MAPK8), and these increases were significantly inhibited by exendin-4 treatment. HG/PA treatment of INS-1 cells increased SREBP1 (SREBF1) protein and induced its nuclear translocation and subsequently increased C/EBPβ (CEBPB) protein and its nuclear translocation. Exendin-4 treatment attenuated this increase. Knockdown of <I>SREBP1c</I> reduced the activation of <I>C/EBP</I><I>β</I> and also blocked the expression of ER stress markers induced by HG/PA treatment. Our results indicate that exendin-4 inhibits the activation of SREBP1c and C/EBPβ, which, in turn, may reduce glucolipotoxicity-induced ER stress and β-cell apoptosis.</P>