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Nuñ,ez, Ana J.,Shear, Lindsey N.,Dahal, Naween,Ibarra, Ilich A.,Yoon, JiWoong,Hwang, Young Kyu,Chang, Jong-San,Humphrey, Simon M. Royal Society of Chemistry 2011 Chemical communications Vol.47 No.43
<P>PCM-10 is a porous phosphine coordination material based on Ca(<SMALL>II</SMALL>) and <I>tris</I>(<I>p</I>-carboxylated) triphenylphosphine. The material provides a unique 3-dimensional surface of P(<SMALL>III</SMALL>) Lewis base sites, which is ideal for post-synthetic functionalization. The addition of Au(<SMALL>I</SMALL>) yields an advanced material that can selectively adsorb 1-hexene over n-hexane at room temperature.</P> <P>Graphic Abstract</P><P>The 3-dimensional porous coordination polymer, PCM-10, is based on triphenylphosphine. The free phosphine sites within the polymer may be post-synthetically modified with catalytic species, such as AuCl. <IMG SRC='http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=c1cc14682c'> </P>
Lung-Chun Huang,Wen-San Huang,Chung-Ping Lin,Olga M. Nuñeza,Hui-Yun Tseng,Hsin-Chieh Tang 한국응용곤충학회 2018 Journal of Asia-Pacific Entomology Vol.21 No.4
Endemic species of oceanic islands are vulnerable due to their geographical isolation and small population sizes. For endangered island species, captive breeding program is an important strategy for conservation and sustainable management. Pachyrhynchus sarcitis is a flightless weevil decorated with colourful markings and distributed exclusively on several islets of Southeast Asia including Lanyu, Ludao, and Babuyan Islands. The life history of threatened Pachyrhynchus species of these islands was poorly known. This study reared P. sarcitis from Lanyu and Babuyan Islands for the first time in the laboratory using their host plant (Leea guineensis). The two island populations showed significant differences in instar numbers, in which the weevils from Lanyu Island had a higher instar number regardless the length of developmental duration. The adult body size of both sexes of the Babuyan population became smaller under laboratory condition; whereas Lanyu population in the laboratory did not show this trend. The differences in larval development might suggest local adaptation to the host plants or other life history associated characteristics which requires further research.
Lee Eunhyeong,Lee Eun-Ah,Kong Eunji,Chon Haemin,Llaiqui-Condori Melissa,Park Cheon Ho,Park Beom Yong,Kang Nu Ri,Yoo Jin-San,Lee Hyun-Soo,Kim Hyung Seok,Park Sung-Hong,Choi Seung-Won,Vestweber Dietmar 생화학분자생물학회 2023 Experimental and molecular medicine Vol.55 No.-
Tumor progression is intimately associated with the vasculature, as tumor proliferation induces angiogenesis and tumor cells metastasize to distant organs via blood vessels. However, whether tumor invasion is associated with blood vessels remains unknown. As glioblastoma (GBM) is featured by aggressive invasion and vascular abnormalities, we characterized the onset of vascular remodeling in the diffuse tumor infiltrating zone by establishing new spontaneous GBM models with robust invasion capacity. Normal brain vessels underwent a gradual transition to severely impaired tumor vessels at the GBM periphery over several days. Increasing vasodilation from the tumor periphery to the tumor core was also found in human GBM. The levels of vascular endothelial growth factor (VEGF) and VEGF receptor 2 (VEGFR2) showed a spatial correlation with the extent of vascular abnormalities spanning the tumor-invading zone. Blockade of VEGFR2 suppressed vascular remodeling at the tumor periphery, confirming the role of VEGF-VEGFR2 signaling in the invasion-associated vascular transition. As angiopoietin-2 (ANGPT2) was expressed in only a portion of the central tumor vessels, we developed a ligand-independent tunica interna endothelial cell kinase 2 (Tie2)-activating antibody that can result in Tie2 phosphorylation in vivo. This agonistic anti-Tie2 antibody effectively normalized the vasculature in both the tumor periphery and tumor center, similar to the effects of VEGFR2 blockade. Mechanistically, this antibody-based Tie2 activation induced VE-PTP-mediated VEGFR2 dephosphorylation in vivo. Thus, our study reveals that the normal-to-tumor vascular transition is spatiotemporally associated with GBM invasion and may be controlled by Tie2 activation via a novel mechanism of action.