Unknown

Dataset Information

0

Human Alpha 1 Antitrypsin Suppresses NF-κB Activity and Extends Lifespan in Adult Drosophila.


ABSTRACT: Human alpha 1 antitrypsin (hAAT) is a multifunctional protein that has been shown to have anti-inflammatory and cellular protective properties. While previous studies demonstrated the antiaging potential of hAAT, the mechanism(s) underlying the antiaging effect remain elusive. In this study, we performed a detailed analysis of transcriptomic data that indicated that NF-κB-targeted genes and NF-κB-regulated pathways were selectively inhibited by hAAT treatment. We further showed that the first detectable impact of hAAT treatment was the inhibition of the nuclear activity of NF-κB. Subsequently, hAAT treatment suppressed the mRNA levels of NF-κB-targeted genes, as well as NF-κB itself (P65 and P50), in human senescent cells. Using Drosophila models, we further examined the impact of hAAT on locomotor activity and endurance. Finally, using an adult-specific promotor, we demonstrated that overexpression of hAAT in the late stage of life significantly extended the lifespan of transgenic flies. These results extend the current understanding of the anti-inflammatory function of hAAT.

SUBMITTER: Yuan Y 

PROVIDER: S-EPMC9599126 | biostudies-literature | 2022 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

Human Alpha 1 Antitrypsin Suppresses NF-κB Activity and Extends Lifespan in Adult <i>Drosophila</i>.

Yuan Ye Y   Van Belkum Max M   O'Brien Alana A   Garcia Alain A   Troncoso Karla K   Elshikha Ahmed S AS   Zhou Lei L   Song Sihong S  

Biomolecules 20220922 10


Human alpha 1 antitrypsin (hAAT) is a multifunctional protein that has been shown to have anti-inflammatory and cellular protective properties. While previous studies demonstrated the antiaging potential of hAAT, the mechanism(s) underlying the antiaging effect remain elusive. In this study, we performed a detailed analysis of transcriptomic data that indicated that NF-κB-targeted genes and NF-κB-regulated pathways were selectively inhibited by hAAT treatment. We further showed that the first de  ...[more]

Similar Datasets

| S-EPMC10698029 | biostudies-literature
| S-EPMC6629006 | biostudies-literature
| S-EPMC2759400 | biostudies-literature
| S-EPMC4191686 | biostudies-literature
| S-EPMC4595730 | biostudies-literature
| S-EPMC7744100 | biostudies-literature
| S-EPMC2830081 | biostudies-literature
| S-EPMC3769260 | biostudies-other
| S-EPMC7803524 | biostudies-literature
| S-EPMC8501845 | biostudies-literature