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The non‐consumptive effects of predator‐induced stress can influence a variety of life‐history traits. Many previous studies focused only on short‐term effects such as development and reproductive rates. Recent studies have showed that long‐term predation stress (given during the whole life of the prey) and short‐term predation stress (provided during the immature stage of the prey) could generate completely opposite results: the former could decrease lifespan, whereas the later could increase lifespan. However, it is still unclear whether the advantage is because of the short duration of exposure or the early stage of life during which exposure was exerted. Thus, in this study, the prey (Tyrophagus putrescentiae) was exposed to predation stress from the predator (Neoseiulus cucumeris) during different life stages (larva, protonymph, tritonymph, first 5 d of oviposition, the full lifespan or none of the above). The results showed that the predation stress supplied during larval and protonymphal stage delayed development, reduced fecundity and prolonged lifespan of the prey, while the stress given during tritonymphal stage only reduced lifespan slightly and the stress given during the first 5 d of oviposition did not change lifespan but reduced fecundity. This study indicated that the effects of predation stress are dependent on prey life stage and the predation stress experienced in the early life stages is important to lifespan modulation. [ABSTRACT FROM AUTHOR]

Mesenchymal stem cells (MSCs) play important roles in tissue regeneration due to their self-renewal, multilineage differentiation and immunosuppression abilities. MSCs can be isolated from various kinds of tissue, such as umbilical cord, cord blood and placenta. Human placenta mesenchymal stem cells (hPMSCs) possess stronger immunosuppressive properties, such as the ability to inhibit T-cell activation and proliferation, than human bone marrow MSCs. We have investigated that the roles of the programmed death ligands 1 and 2 (PDL1 and PDL2) in hPMSC adhesion, migration and immunosuppression were investigated. PDL1 and PDL2 were highly expressed by hPMSCs. Knockdown of PDL1 and/or PDL2 by siRNA increased hPMSC adhesion, but greatly decreasing migration. PDL1 and PDL2 expressed on hPMSCs inhibited T-cell proliferation by arresting the cell cycle. Knockdown of PDL1 and/or PDL2 in hPMSCs, however, had no effect on the expression of CD69, a T-cell early activation marker found on both CD4+ and CD8+ T-cell subsets. In summary, the roles of the negative co-stimulators PDL1 and PDL2 is on the adhesion, migration and immunosuppression of hPMSCs. These findings may be useful regarding the potential use of hPMSCs in clinical cell. [ABSTRACT FROM AUTHOR]