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Length–weight and length–length relationships of seven fish species from the Ili River and tributaries,northwest China
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Z.‐M. Zhang C.‐X. Xie H.‐P. Ding X.‐F. Ma C.‐J. Liu Y. Guo 《Zeitschrift fur angewandte Ichthyologie》2016,32(1):153-155
Length–weight and length–length relationships were estimated for seven fish species belonging to four families from the Ili River and its tributaries, northwest China. From April to October 2013 and May to October 2014, specimens were collected monthly for a total of 783 specimens. This study presents the first references on LWRs for Diptychus maculates, Gymnodiptychu dybowskii, Perca schrenkii, Silurus meridionalis and Schizothorax pseudoaksaiensis pseudoaksaiensis, and LLRs for G. dybowskii, P. schrenkii, S. meridionalis, S. pseudoaksaiensis pseudoaksaiensis, Triplophysa strauchii and Triplophysa stoliczkai. 相似文献
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828.
Phytophthora capsici homologue of the cell cycle regulator SDA1 is required for sporangial morphology,mycelial growth and plant infection
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SDA1 encodes a highly conserved protein that is widely distributed in eukaryotic organisms. SDA1 is essential for cell cycle progression and organization of the actin cytoskeleton in yeasts and humans. In this study, we identified a Phytophthora capsici orthologue of yeast SDA1, named PcSDA1. In P. capsici, PcSDA1 is strongly expressed in three asexual developmental states (mycelium, sporangia and germinating cysts), as well as late in infection. Silencing or overexpression of PcSDA1 in P. capsici transformants affected the growth of hyphae and sporangiophores, sporangial development, cyst germination and zoospore release. Phalloidin staining confirmed that PcSDA1 is required for organization of the actin cytoskeleton. Moreover, 4′,6‐diamidino‐2‐phenylindole (DAPI) staining and PcSDA1‐green fluorescent protein (GFP) fusions revealed that PcSDA1 is involved in the regulation of nuclear distribution in hyphae and sporangia. Both silenced and overexpression transformants showed severely diminished virulence. Thus, our results suggest that PcSDA1 plays a similar role in the regulation of the actin cytoskeleton and nuclear division in this filamentous organism as in non‐filamentous yeasts and human cells. 相似文献
829.
Yujuan Su Shenglian Yang Kechun Zhou Yani Liu Ju Cheng Dunguo Lu Liu Fan Yizheng Wang 《EMBO reports》2016,17(5):682-694
Sonic hedgehog (Shh), both as a mitogen and as a morphogen, plays an important role in cell proliferation and differentiation during early development. Here, we show that Shh inhibits glutamate transporter activities in neurons, rapidly enhances extracellular glutamate levels, and affects the development of epilepsy. Shh is quickly released in response to epileptic, but not physiological, stimuli. Inhibition of neuronal glutamate transporters by Shh depends on heterotrimeric G protein subunit Gαi and enhances extracellular glutamate levels. Inhibiting Shh signaling greatly reduces epileptiform activities in both cell cultures and hippocampal slices. Moreover, pharmacological or genetic inhibition of Shh signaling markedly suppresses epileptic phenotypes in kindling or pilocarpine models. Our results suggest that Shh contributes to the development of epilepsy and suppression of its signaling prevents the development of the disease. Thus, Shh can act as a modulator of neuronal activity, rapidly regulating glutamate levels and promoting epilepsy. 相似文献
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Xiaojuan Han Haoran Tai Xiaobo Wang Zhe Wang Jiao Zhou Xiawei Wei Yi Ding Hui Gong Chunfen Mo Jie Zhang Jianqiong Qin Yuanji Ma Ning Huang Rong Xiang Hengyi Xiao 《Aging cell》2016,15(3):416-427
AMPK activation is beneficial for cellular homeostasis and senescence prevention. However, the molecular events involved in AMPK activation are not well defined. In this study, we addressed the mechanism underlying the protective effect of AMPK on oxidative stress‐induced senescence. The results showed that AMPK was inactivated in senescent cells. However, pharmacological activation of AMPK by metformin and berberine significantly prevented the development of senescence and, accordingly, inhibition of AMPK by Compound C was accelerated. Importantly, AMPK activation prevented hydrogen peroxide‐induced impairment of the autophagic flux in senescent cells, evidenced by the decreased p62 degradation, GFP‐RFP‐LC3 cancellation, and activity of lysosomal hydrolases. We also found that AMPK activation restored the NAD+ levels in the senescent cells via a mechanism involving mostly the salvage pathway for NAD+ synthesis. In addition, the mechanistic relationship of autophagic flux and NAD+ synthesis and the involvement of mTOR and Sirt1 activities were assessed. In summary, our results suggest that AMPK prevents oxidative stress‐induced senescence by improving autophagic flux and NAD+ homeostasis. This study provides a new insight for exploring the mechanisms of aging, autophagy and NAD+ homeostasis, and it is also valuable in the development of innovative strategies to combat aging. 相似文献