[Vegetation carbon stocks and net primary productivity of the mangrove forests in Shenzhen, China.] / æ·±åœ³ç¦ç”°çº¢æ ‘æž—æ¤è¢«ç¢³å‚¨é‡å’Œå‡€åˆçº§ç”Ÿäº§åŠ›.

Mangroves are the most important coastal blue carbon sinks. The accurate estimation on the carbon sequestration capacity of plant communities would guide the mangrove conservation, afforestation and management. This study investigated the vegetation carbon stocks of dominant mangrove communities, which were Avicennia marina, Kandelia obovata, Sonneratia caseolaris, and Sonneratia apetala in Futian Nature Mangrove Reserve in Shenzhen, Guangdong Province of China. Vegetation carbon stock consisted of living trees (aboveground and belowground biomass), understory, pneumatophore, standing dead trees, fallen dead trees and litter in these communities. The net primary productivity (NPP) was calculated from the litterfall and incremental growth in the same year of each community. Our results showed that the vegetation carbon stocks for A. marina, K. obovata, S. caseolaris, and S. apetala communities were 28.7, 127.6, 100.1, and 73.6 t C·hm-2, and the NPP were 8.75, 7.67, 9.60, and 11.8 t C·hm-2·a-1, respectively. Therefore, acting as urban forests, Futian mangroves in Shenzhen assimilated about 4000 t CO2·a-1. These results provided guidance for mangrove blue carbon assessment, and theoretical basis for the construction of coastal carbon sequestration forests in China.

Multi-target lentivirus specific to hepatocellular carcinoma: in vitro and in vivo studies.

BACKGROUND & AIMS: We aimed at investigating the effects of the targeted transduction of the Wtp53-pPRIME-miR30-shRNA gene into liver cancer cells, under the mediation of anti-alpha fetoprotein scFv-directed lentivirus, and the inhibitory effect of this system on liver cancer cells. METHODS: The result of infection was observed by fluorescence microscopy. Polymerase chain reaction and Western blotting were used to demonstrate the successful transduction and transcription of the Wtp53-pPRIME-miR30-shRNA-IGF1R gene. Cell growth was observed via the Cell-Counting Kit-8 Method, and cell apoptosis was detected by terminal deoxynucleotidyl transferase biotin-dUTP nick end labeling. To observe further the effects of AFP-Wtp53-pPRIME-miR30-shRNA-IGF1R therapy in animals, models of BALB-C nude mice bearing subcutaneous human hepatocellular carcinoma were established. The influence of the growth of subcutaneously transplanted tumor, expression of Wtp53 protein, apoptosis, and microvessel formation on the overall level of AFP-Wtp53 pPRIME-miR30-shRNA-IGF1R were also evaluated. RESULTS: Recombinant lentivirus was successfully constructed, and its functional plaque-forming unit titer was determined as 4.58 × 10(9)plaque-forming units/ml. A positive strand was detected by polymerase chain reaction and Western blotting. Lentiviral construction worked effectively in AFP-positive liver cancer cells. In vitro and in vivo experiments showed that the recombinant lentivirus was more efficacious in inhibiting the proliferation of Hep3B cells. CONCLUSIONS: The Wtp53-pPRIME-miR30-shRNA gene can be subjected to targeted transduction into liver cancer cells under the mediation of anti-alpha fetoprotein scFv-directed lentivirus. The Wtp53-pPRIME-miR30-shRNA system has targeting ability and lethal effects on liver cancer cells.