Data_Sheet_1_Soil nematode community assembly in a primary tropical lowland rainforest.docx

More than half of the world's tropical lowland rainforests have been lost due to conversion to agricultural land (such as rubber plantations). Thus, ecological restoration in degraded tropical lowland rainforests is crucial. The first step to restoration is restoring soil functioning (i.e., soil fertility, carbon, and nitrogen cycling) to levels similar to those in the primary tropical lowland rainforest. This requires understanding soil nematode community assembly in primary tropical lowland rainforest, which has never been explored in this habitat. In this study, we measured species compositions of plant and soil nematode communities and soil characteristics (pH, total and available nitrogen, phosphorus, and soil water content) in a primary tropical lowland rainforest, which is located on Hainan Island, China. We performed two tests (the null-model test and distance-based Moran's eigenvector maps (MEM) and redundancy analysis-based variance partitioning) to quantify the relative contribution of the deterministic (abiotic filtering and biotic interactions) and stochastic processes (random processes and dispersal limitation) to the soil nematode community. We found that a deterministic process (habitat filtering) determined nematode community assembly in our tropical lowland rainforest. Moreover, soil properties, but not plant diversity, were the key determinants of nematode community assembly. We have, for the first time, managed to identify factors that contribute to the nematode community assembly in the tropical lowland rainforest. This quantified community assembly mechanism can guide future soil functioning recovery of the tropical lowland rainforest.</p

Apolipoprotein CIII regulates lipoprotein-associated phospholipase A2 expression via the MAPK and NFκB pathways

Apolipoprotein CIII (apo CIII), a small glycoprotein that binds to the surfaces of certain lipoproteins, is associated with inflammatory and atherogenic responses in vascular cells. Lipoprotein-associated phospholipase A2 (Lp-PLA2) has been proposed as an inflammatory biomarker and potential therapeutic target for cardiovascular disease (CVD). Here, we report that apo CIII increases Lp-PLA2 mRNA and protein levels in dose- and time- dependent manner in human monocytic THP-1 cells, and the increase can be abolished by MAPK and NFκB pathway inhibitors. Lp-PLA2 inhibitor, 1-linoleoyl glycerol attenuates the inflammation induced by apo CIII. In turn, exogenous Lp-PLA2 expression upregulates apo CIII and the upregulation can be inhibited by 1-linoleoyl glycerol in HepG2 cells. Moreover, plasma Lp-PLA2 level is correlated with apo CIII expression in pig liver. In vivo, Lp-PLA2 expression in monocytes and its activity in serum were significantly increased in human apo CIII transgenic porcine models compared with wild-type pigs. Our results suggest that Lp-PLA2 and apo CIII expression level is correlated with each other in vitro and in vivo