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美国政府资助26亿美元用于保护沿海社区和恢复海洋资源 快报文章
资源环境快报,2023年第12期
作者:  董利苹
Microsoft Word(22Kb)  |  收藏  |  浏览/下载:548/0  |  提交时间:2023/06/29
$2.6 billion  protect coastal communities  restore marine resources  
UNEP世界各地脆弱的山区生态系统正在好转 快报文章
资源环境快报,2022年第24期
作者:  吴秀平
Microsoft Word(17Kb)  |  收藏  |  浏览/下载:408/1  |  提交时间:2023/01/01
mountain ecosystems  protect  
SIWI指出政府保护地下水的5种方法 快报文章
资源环境快报,2022年第05期
作者:  吴秀平
Microsoft Word(13Kb)  |  收藏  |  浏览/下载:732/1  |  提交时间:2022/03/16
Groundwater  government  protect  
加拿大投资2500万加元保护大草原地区的湿地与草原 快报文章
资源环境快报,2021年第15期
作者:  裴惠娟
Microsoft Word(13Kb)  |  收藏  |  浏览/下载:504/0  |  提交时间:2021/08/16
Canada  Protect  Wetlands and Grasslands  
新研究显示只有17%的自由流动河流得到保护 快报文章
资源环境快报,2021年第10期
作者:  吴秀平
Microsoft Word(21Kb)  |  收藏  |  浏览/下载:426/0  |  提交时间:2021/05/31
free-flowing rivers  freshwater system  protect  
A dominant autoinflammatory disease caused by non-cleavable variants of RIPK1 期刊论文
NATURE, 2020, 577 (7788) : 109-+
作者:  Tao, Panfeng;  Sun, Jinqiao;  Wu, Zheming;  Wang, Shihao;  Wang, Jun;  Li, Wanjin;  Pan, Heling;  Bai, Renkui;  Zhang, Jiahui;  Wang, Ying;  Lee, Pui Y.;  Ying, Wenjing;  Zhou, Qinhua;  Hou, Jia;  Wang, Wenjie;  Sun, Bijun;  Yang, Mi;  Liu, Danru;  Fang, Ran;  Han, Huan;  Yang, Zhaohui;  Huang, Xin;  Li, Haibo;  Deuitch, Natalie;  Zhang, Yuan;  Dissanayake, Dilan;  Haude, Katrina;  McWalter, Kirsty;  Roadhouse, Chelsea;  MacKenzie, Jennifer J.;  Laxer, Ronald M.;  Aksentijevich, Ivona;  Yu, Xiaomin;  Wang, Xiaochuan;  Yuan, Junying;  Zhou, Qing
收藏  |  浏览/下载:28/0  |  提交时间:2020/07/03

Activation of RIPK1 controls TNF-mediated apoptosis, necroptosis and inflammatory pathways(1). Cleavage of human and mouse RIPK1 after residues D324 and D325, respectively, by caspase-8 separates the RIPK1 kinase domain from the intermediate and death domains. The D325A mutation in mouse RIPK1 leads to embryonic lethality during mouse development(2,3). However, the functional importance of blocking caspase-8-mediated cleavage of RIPK1 on RIPK1 activation in humans is unknown. Here we identify two families with variants in RIPK1 (D324V and D324H) that lead to distinct symptoms of recurrent fevers and lymphadenopathy in an autosomaldominant manner. Impaired cleavage of RIPK1 D324 variants by caspase-8 sensitized patients'  peripheral blood mononuclear cells to RIPK1 activation, apoptosis and necroptosis induced by TNF. The patients showed strong RIPK1-dependent activation of inflammatory signalling pathways and overproduction of inflammatory cytokines and chemokines compared with unaffected controls. Furthermore, we show that expression of the RIPK1 mutants D325V or D325H in mouse embryonic fibroblasts confers not only increased sensitivity to RIPK1 activation-mediated apoptosis and necroptosis, but also induction of pro-inflammatory cytokines such as IL-6 and TNF. By contrast, patient-derived fibroblasts showed reduced expression of RIPK1 and downregulated production of reactive oxygen species, resulting in resistance to necroptosis and ferroptosis. Together, these data suggest that human non-cleavable RIPK1 variants promote activation of RIPK1, and lead to an autoinflammatory disease characterized by hypersensitivity to apoptosis and necroptosis and increased inflammatory response in peripheral blood mononuclear cells, as well as a compensatory mechanism to protect against several pro-death stimuli in fibroblasts.


  
The first dinosaur egg was soft 期刊论文
NATURE, 2020
作者:  Rodstrom, Karin E. J.;  Kiper, Aytug K.;  Zhang, Wei;  Rinne, Susanne;  Pike, Ashley C. W.;  Goldstein, Matthias;  Conrad, Linus J.;  Delbeck, Martina;  Hahn, Michael G.;  Meier, Heinrich;  Platzk, Magdalena;  Quigley, Andrew;  Speedman, David;  Shrestha, Leela;  Mukhopadhyay, Shubhashish M. M.
收藏  |  浏览/下载:48/0  |  提交时间:2020/07/03

Molecular analyses of newly discovered, embryo-bearing ornithischian and sauropod dinosaur eggs suggest that the ancestral dinosaur egg was soft-shelled, and that hard-shelled eggs evolved independently at least three times in the major dinosaur lineages.


Calcified eggshells protect developing embryos against environmental stress and contribute to reproductive success(1). As modern crocodilians and birds lay hard-shelled eggs, this eggshell type has been inferred for non-avian dinosaurs. Known dinosaur eggshells are characterized by an innermost membrane, an overlying protein matrix containing calcite, and an outermost waxy cuticle(2-7). The calcitic eggshell consists of one or more ultrastructural layers that differ markedly among the three major dinosaur clades, as do the configurations of respiratory pores. So far, only hadrosaurid, a few sauropodomorph and tetanuran eggshells have been discovered  the paucity of the fossil record and the lack of intermediate eggshell types challenge efforts to homologize eggshell structures across all dinosaurs(8-18). Here we present mineralogical, organochemical and ultrastructural evidence for an originally non-biomineralized, soft-shelled nature of exceptionally preserved ornithischianProtoceratopsand basal sauropodomorphMussauruseggs. Statistical evaluation of in situ Raman spectra obtained for a representative set of hard- and soft-shelled, fossil and extant diapsid eggshells clusters the originally organic but secondarily phosphatizedProtoceratopsand the organicMussauruseggshells with soft, non-biomineralized eggshells. Histology corroborates the organic composition of these soft-shelled dinosaur eggs, revealing a stratified arrangement resembling turtle soft eggshell. Through an ancestral-state reconstruction of composition and ultrastructure, we compare eggshells fromProtoceratopsandMussauruswith those from other diapsids, revealing that the first dinosaur egg was soft-shelled. The calcified, hard-shelled dinosaur egg evolved independently at least three times throughout the Mesozoic era, explaining the bias towards eggshells of derived dinosaurs in the fossil record.


  
Where I work Andrew Digby 期刊论文
NATURE, 2020, 580 (7804) : 556-556
作者:  Archard, David;  Dabrock, Peter;  Delfraissy, Jean-Francois
收藏  |  浏览/下载:5/0  |  提交时间:2020/07/03

Andrew Digby works to protect the kakapo, a critically endangered and charismatic New Zealand species of parrot.


Andrew Digby works to protect the kakapo, a critically endangered and charismatic New Zealand species of parrot.


  
REFUGEE CAMPS RACE TO AVERT CORONAVIRUS CATASTROPHE 期刊论文
NATURE, 2020, 581 (7806) : 18-18
作者:  Schewe, Phillip F.
收藏  |  浏览/下载:1/0  |  提交时间:2020/07/03

From Bangladesh to Somalia, researchers and aid workers are taking different steps to protect people among the most vulnerable to the pandemic.


From Bangladesh to Somalia, researchers and aid workers are taking different steps to protect people among the most vulnerable to the pandemic.


  
Decoy exosomes provide protection against bacterial toxins 期刊论文
NATURE, 2020, 579 (7798) : 260-+
作者:  Park, Jin Suk;  Burckhardt, Christoph J.;  Lazcano, Rossana;  Solis, Luisa M.;  Isogai, Tadamoto;  Li, Linqing;  Chen, Christopher S.;  Gao, Boning;  Minna, John D.;  Bachoo, Robert;  DeBerardinis, Ralph J.;  Danuser, Gaudenz
收藏  |  浏览/下载:17/0  |  提交时间:2020/07/03

The production of pore-forming toxins that disrupt the plasma membrane of host cells is a common virulence strategy for bacterial pathogens such as methicillin-resistant Staphylococcus aureus (MRSA)(1-3). It is unclear, however, whether host species possess innate immune mechanisms that can neutralize pore-forming toxins during infection. We previously showed that the autophagy protein ATG16L1 is necessary for protection against MRSA strains encoding alpha-toxin(4)-a pore-forming toxin that binds the metalloprotease ADAM10 on the surface of a broad range of target cells and tissues(2,5,6). Autophagy typically involves the targeting of cytosolic material to the lysosome for degradation. Here we demonstrate that ATG16L1 and other ATG proteins mediate protection against alpha-toxin through the release of ADAM10 on exosomes-extracellular vesicles of endosomal origin. Bacterial DNA and CpG DNA induce the secretion of ADAM10-bearing exosomes from human cells as well as in mice. Transferred exosomes protect host cells in vitro by serving as scavengers that can bind multiple toxins, and improve the survival of mice infected with MRSA in vivo. These findings indicate that ATG proteins mediate a previously unknown form of defence in response to infection, facilitating the release of exosomes that serve as decoys for bacterially produced toxins.