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Paisner, R.

Publications and source records attributed to Paisner, R..

2 recordsLinked to original sources

The Maternal Effect of SKN-1B and DAF-7 on Intergenerational Pathogen Avoidance Learning in C. elegans.

Parental health strongly influences the development of embryos, and can ultimately influence behavior post-birth. When exposed to pathogenic Pseudomonas aeruginosa (PA14), C. elegans produces a robust immune response, as well as a learned behavior to avoid PA14 in the future. This learned avoidance of PA14 can be inherited by the F1 generation. An important trigger of the worms immune response to infection is the Nrf2 homologue, SKN-1. We find that the SKN-1B isoform strongly influences the intergenerational inheritance of PA14 avoidance in F1 animals via DAF-7 (TGF-{beta}) signaling from ASI. Functional SKN-1B is required in both the P0 and F1 generations to facilitate F1 avoidance of PA14 due to parental exposure. While inherited avoidance of PA14 was not observed in F2+ generations, the single generation learning investigated here may provide a parallel pathway to improve the fitness of F1 animals in a dynamic environment.

neuroscience↗

Oncogene Regulated Release of Extracellular Vesicles

Oncogenes can alter cellular structure, function, development and metabolism including changing the balance between anabolic and catabolic processes. However, how oncogenes regulate tumor cell biomass remains poorly understood. Using isogenic mammary breast epithelial cells transformed with a panel of ten oncogenes found commonly mutated, amplified or overexpressed in multiple cancers, we show that specific oncogenes reduce the biomass of cancer cells by promoting extracellular vesicle release. While MYC and AURKB elicited the highest number of EVs, each oncogene tested selectively altered the protein composition of released EVs. Likewise, miRNAs were differentially sorted into EVs in an oncogene-specific manner. MYC overexpressing cells require ceramide, while AURKB require ESCRT to release high levels of EVs. Finally, lysosome-associated genes are broadly downregulated in the context of MYC and AURKB, suggesting that cellular contents instead of being degraded, were released via EVs. Thus, oncogene mediated biomass regulation via differential EV release is a new metabolic phenotype which may have implications for cellular signaling and homeostasis.

cell biology↗