JAG1 mediates apoptosis in herpes simplex keratitis by suppressing autophagy via ROS/JAG1/NOTCH1/pULK1 signaling pathway DOI Creative Commons
Jingyao Chang,

Yao Yao,

Xinghong Sun

и другие.

Cell Biology and Toxicology, Год журнала: 2024, Номер 41(1)

Опубликована: Дек. 20, 2024

Herpes simplex keratitis (HSK), an ocular disease resulted from herpes virus type 1 (HSV-1) infection, leads to the majority of infectious corneal blindness worldwide. The apoptosis epithelial cells (CECs) HSV-1 disrupts barrier and exacerbates infection; however, there is no definitive cure for HSK. Jagged1 (JAG1), one primary functional ligands NOTCH receptors, plays a crucial role in regulating autophagy; its HSK unclear. Our transcriptome analysis showed JAG1 was significantly upregulated HSV-1-infected human CECs. We aimed explore JAG1's CECs mice. infection induced reactive oxygen species (ROS) generation also activated JAG1/NOTCH1 signaling pathway. ROS scavenger N-acetylcysteine mitigated these effects. Additionally, inhibiting pathway with short hairpin RNA against or NOTCH1 inhibitor (N-[N-{3,5-difuorophenacetyl}-1-alanyl]-S-phenylglycine t-butyl ester [DAPT]) alleviated HSV-1-induced CEC apoptosis. Transmission electron microscopy western blotting revealed that suppressed ULK1-mediated autophagy CECs, while DAPT treatment enhanced by suppressing ULK1 phosphorylation. activation rapamycin markedly reduced levels revealing synergistic effect between increased levels, ultimately leading Thus, induces through ROS/JAG1/NOTCH1/pULK1 vitro vivo, providing potential therapeutic targets

Язык: Английский

NRF2-mediated regulation of lipid pathways in viral infection DOI
Khursheed Muzammil,

Zahraa Sabah Ghnim,

Ibrahim Saeed Gataa

и другие.

Molecular Aspects of Medicine, Год журнала: 2024, Номер 97, С. 101279 - 101279

Опубликована: Май 20, 2024

Язык: Английский

Процитировано

7

Korean Black Ginseng Extract Alleviates Alzheimer’s Disease-Related Cognitive Impairment by Activating the Nrf2/HO-1 Pathway and Suppressing the p38 MAPK/NF-κB/STAT3 Pathways and NLRP3 Inflammasome via TLR2 and TLR4 Modulation DOI Creative Commons
Yujeong Ha,

Hyo-Sung Jo,

Tae Woo Kwon

и другие.

Journal of Ginseng Research, Год журнала: 2025, Номер unknown

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

Anti-Colorectal Cancer Activity of Panax and Its Active Components, Ginsenosides: A Review DOI Open Access

Hyun-Su Kang,

Hyun Lim, Won Young Jang

и другие.

International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(6), С. 2593 - 2593

Опубликована: Март 13, 2025

Colorectal cancer (CRC) poses a significant health burden worldwide and necessitates novel treatment approaches with fewer side effects than conventional chemotherapy. Many natural compounds have been tested as possible treatments. Plants in the genus Panax widely studied due to their therapeutic potential for various diseases such inflammatory disorders cancers. Extracts from plants of activate upstream signals, including those related autophagy generation reactive oxygen species, induce intrinsic apoptosis CRC cells. The root extract notoginseng (P. notoginseng) regulated gut microbiota enhance T-cell-induced immune response against CRC. Protopanaxadiol (PPD)-type ginsenosides, especially Rh2, Rg3, Rb1, Rb2, significantly reduced proliferation cells tumor size xenograft mouse model, well targeting programmed death (PD)-1 block checkpoint Moreover, modified nanocarriers ginsenosides upregulated drug efficacy, showing that can also be utilized carriers. An increasing body studies has demonstrated curing Ginsenosides are promising active Panax, which support activity therapies.

Язык: Английский

Процитировано

0

Protective effect of ginseng berry saponin conversion products on skin photodamage caused by UVB in vitro and in vivo DOI

Hongyan Tan,

Honghong Ren,

Jiayi Chai

и другие.

Food Research International, Год журнала: 2024, Номер 198, С. 115379 - 115379

Опубликована: Ноя. 20, 2024

Язык: Английский

Процитировано

2

Antiviral potential of ginseng: Targeting human pathogenic viruses with compounds derived from ginseng DOI Creative Commons
Chen Huo,

Ji-hye Baek,

Ki Hyun Kim

и другие.

Journal of Ginseng Research, Год журнала: 2024, Номер 49(2), С. 105 - 117

Опубликована: Дек. 10, 2024

The COVID-19 pandemic has highlighted the critical need for effective antiviral therapies, as viral infections remain a leading cause of mortality worldwide. Natural compounds, especially those derived from plants, have been recognized their therapeutic properties. Ginseng, in particular, attracted considerable attention its potential effects. This review examines compounds ginseng that act against various human pathogenic viruses. We systematically summarize activities targeting range viruses, including rhinovirus (HRV), influenza virus, immunodeficiency virus (HIV), hepatitis viruses A, B, and C (HAV, HBV, HCV), herpes simplex (HSV), enterovirus 71 (EV71), coxsackievirus, norovirus, SARS-CoV-2, responsible COVID-19. covers Panax ginseng, P. notoginseng, quinquefolius, discussing mechanisms action potential. analysis incorporates literature February 2002 through August 2024, providing comprehensive overview existing evidence on properties ginseng. aims to underscore scientific basis developing an agent or nutraceutical.

Язык: Английский

Процитировано

1

JAG1 mediates apoptosis in herpes simplex keratitis by suppressing autophagy via ROS/JAG1/NOTCH1/pULK1 signaling pathway DOI Creative Commons
Jingyao Chang,

Yao Yao,

Xinghong Sun

и другие.

Cell Biology and Toxicology, Год журнала: 2024, Номер 41(1)

Опубликована: Дек. 20, 2024

Herpes simplex keratitis (HSK), an ocular disease resulted from herpes virus type 1 (HSV-1) infection, leads to the majority of infectious corneal blindness worldwide. The apoptosis epithelial cells (CECs) HSV-1 disrupts barrier and exacerbates infection; however, there is no definitive cure for HSK. Jagged1 (JAG1), one primary functional ligands NOTCH receptors, plays a crucial role in regulating autophagy; its HSK unclear. Our transcriptome analysis showed JAG1 was significantly upregulated HSV-1-infected human CECs. We aimed explore JAG1's CECs mice. infection induced reactive oxygen species (ROS) generation also activated JAG1/NOTCH1 signaling pathway. ROS scavenger N-acetylcysteine mitigated these effects. Additionally, inhibiting pathway with short hairpin RNA against or NOTCH1 inhibitor (N-[N-{3,5-difuorophenacetyl}-1-alanyl]-S-phenylglycine t-butyl ester [DAPT]) alleviated HSV-1-induced CEC apoptosis. Transmission electron microscopy western blotting revealed that suppressed ULK1-mediated autophagy CECs, while DAPT treatment enhanced by suppressing ULK1 phosphorylation. activation rapamycin markedly reduced levels revealing synergistic effect between increased levels, ultimately leading Thus, induces through ROS/JAG1/NOTCH1/pULK1 vitro vivo, providing potential therapeutic targets

Язык: Английский

Процитировано

1