ALDH1A1 Inhibits Chicken Preadipocytes' Proliferation and Differentiation via the PPARγ Pathway In Vitro and In Vivo
(aldehyde dehydrogenase 1A1) is a crucial protein in retinoids' metabolism, and the lack of inhibits the fat deposition in mice. However, whether has a similar effect on chickens' fat-depot is still unknown. In this study, we investigate the role of in chickens' adipogenesis. The immo...
Gespeichert in:
Veröffentlicht in: | International journal of molecular sciences 2020-04, Vol.21 (9), p.3150 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | (aldehyde dehydrogenase 1A1) is a crucial protein in retinoids' metabolism, and the lack of
inhibits the fat deposition in mice. However, whether
has a similar effect on chickens' fat-depot is still unknown. In this study, we investigate the role of
in chickens' adipogenesis. The immortalized chicken preadipocyte 1 (ICP1) cell line and chicken primary preadipocytes isolated from abdominal fat were used to perform a series of experiments in vitro to elucidate the effects of
. In addition, lentivirus was used to verify the results of cell experiments in vivo. The data showed that overexpression of
significantly weakened the proliferation of preadipocytes and suppressed the differentiation of preadipocytes through the PPARγ pathway, and the knockdown experiments had the opposite results. Moreover, chickens injected with overexpression lentivirus had higher abdominal fat percentage, a bigger size of lipid droplets, and higher triglyceride content in abdominal fat, and chickens injected with interfering lentivirus had the opposite situation. We proved that
not only inhibited the proliferation and differentiation of chickens' preadipocytes in vitro, but also inhibited the fat-depot of chickens in vivo, which was completely opposite the function of
in mice, indicating that
may have a different mechanism that is still unknown. |
---|---|
ISSN: | 1422-0067 1661-6596 1422-0067 |
DOI: | 10.3390/ijms21093150 |