The molecular basis for p53 inhibition of autophagy in porcine fibroblast cells
Autophagy regulation involves an intricate network that can degrade and recycle cytosolic components in autophagosomes when cells are subject to various stress signals. p53 plays a dual role of induction or inhibition in the regulation of autophagy. Recently, pigs have been considered an excellent l...
Saved in:
Published in | Translational cancer research Vol. 8; no. 3; pp. 876 - 886 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
China
AME Publishing Company
01.06.2019
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Autophagy regulation involves an intricate network that can degrade and recycle cytosolic components in autophagosomes when cells are subject to various stress signals. p53 plays a dual role of induction or inhibition in the regulation of autophagy. Recently, pigs have been considered an excellent large animal model for their many anatomical and physiological similarities to humans. Here, we investigated the relationship between p53 and autophagy, as well as the underling molecular basis, in porcine fibroblast cells (PFCs).
Autophagy was induced by Earle's balanced salt solution (EBSS) in p53
and p53
PFCs. The autophagy response was assessed by immunoblotting, transmission electron microscopy (TEM) and fluorescent staining. The molecular basis for p53 regulation of autophagy was analyzed by qPCR.
We found that the increased expression of LC3-II and the decreased expression of P62 occurred earlier in p53
PFCs than in p53
PFCs, the relative autophagic flux of p53
PFCs was stronger than that of p53
PFCs in a time-dependent manner. Meanwhile, we observed a visualized increase of autophagosomes in p53
PFCs. Moreover, we found greater accumulation of LC3 punctate and acidic vesicular organelle (AVOs) in the cytoplasm of p53
PFCs than in that of p53
PFCs, and these effects were further augmented by Baf A1 treatment. Furthermore, we detected the expression of 6 autophagy signaling pathway-related genes and 14 autophagy-related (
) genes by qPCR. We found that the expression patterns of the 6 genes had significant differences in both groups of treated PFCs. These results demonstrated that p53 negatively regulated autophagy and involving the downregulation of LMNA gene by p53 via an unknown pathway, which causes the upregulation of the
,
,
,
and
genes and the downregulation of the
gene.
p53
PFCs responded to autophagy earlier than p53
PFCs, which implied that p53 might inhibit autophagy. The expression patterns of autophagy signaling pathway-related genes and
genes were most different between p53
and p53
PFCs. Our study will provide a new biological model and contribute to further study of the molecular basis for p53 and autophagy. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors contributed equally to this work. Contributions: (I) Conception and design: HY Zhao, HJ Wei; (II) Administrative support: None; (III) Provision of study materials: J Fei, A Xu, Y Liu, D Jiao, W Zeng, H Li; (IV) Collection and assembly of data: A Xu; (V) Data analysis and interpretation: A Xu, HY Zhao, K Xu; (VI): Manuscript writing: All authors; (VII) Final approval of manuscript: All authors. |
ISSN: | 2218-676X 2219-6803 |
DOI: | 10.21037/tcr.2019.05.22 |