scholarly journals Impaired Cellular Energy Metabolism Contributes to Duck-Enteritis-Virus-Induced Autophagy via the AMPK–TSC2–MTOR Signaling Pathway

Author(s):  
Haichang Yin ◽  
Lili Zhao ◽  
Siqi Li ◽  
Lijing Xu ◽  
Yiping Wang ◽  
...  
Nutrients ◽  
2014 ◽  
Vol 6 (12) ◽  
pp. 5500-5516 ◽  
Author(s):  
Jérôme Salles ◽  
Nicolas Cardinault ◽  
Véronique Patrac ◽  
Alexandre Berry ◽  
Christophe Giraudet ◽  
...  

2015 ◽  
Vol 45 (11) ◽  
pp. 1124-1131
Author(s):  
BiE TAN ◽  
FangYuan SHAO ◽  
YuLong YIN ◽  
Hao XIAO ◽  
MiaoMiao WU

Molecules ◽  
2020 ◽  
Vol 25 (17) ◽  
pp. 4004
Author(s):  
Jaeyoon Kim ◽  
Soon Re Kim ◽  
Yun-Ho Choi ◽  
Jae young Shin ◽  
Chang Deok Kim ◽  
...  

The present study aimed to investigate the molecular mechanism of quercitrin, a major constituent of Hottuynia cordata extract, for its hair growth stimulating activities in cultured human dermal papilla cells (hDPCs). Quercitrin enhanced the cell viability and cellular energy metabolism in cultured hDPCs by stimulating the production of NAD(P)H and mitochondrial membrane potential (ΔΨ). The expression of Bcl2, an essential marker for anagen hair follicle and cell survival, was increased by quercitrin treatment. Quercitrin also increased the cell proliferation marker Ki67. The expression of growth factors—such as bFGF, KGF, PDGF-AA, and VEGF—were increased by quercitrin both in mRNA and protein levels. In addition, quercitrin was found to increase the phosphorylation of Akt, Erk, and CREB in cultured hDPCs, while inhibitors of MAPKs reversed the effects of quercitrin. Finally, quercitrin stimulated hair shaft growth in cultured human hair follicles. Our data obtained from present study are in line with those previously reported and demonstrate that quercitrin is (one of) the active compound(s) of Hottuynia cordata extract which showed hair growth promoting effects. It is strongly suggested that the hair growth stimulating activity of quercitrin was exerted by enhancing the cellular energy metabolism, increasing the production of growth factors via activation of MAPK/CREB signaling pathway.


2015 ◽  
Vol 1 (1) ◽  
Author(s):  
Israel C. Nnah ◽  
Khoosheh Khayati ◽  
Radek Dobrowolski

AbstractOver the last few years extensive studies have linked the activity of mTORC1 to lysosomal function. These observations propose an intriguing integration of cellular catabolism, sustained by lysosomes, with anabolic processes, largely controlled by mTORC1. Interestingly, lysosomal function directly affects mTORC1 activity and is regulated by ZKSCAN3 and TFEB, two transcription factors and substrates of mTORC1. Thus, the lysosomal mTOR signaling complex represents a hub of cellular energy metabolism, and its dysregulation may lead to a number of human diseases. Here, we discuss the recent developments and highlight the open questions in this growing field.


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