TY - JOUR
T1 - Activities of curcumin-related compounds in two cell lines persistently infected with different prion strains
AU - Teruya, Kenta
AU - Iwabuchi, Sara
AU - Watanabe, Yuki
AU - Tsuchida, Rikiya
AU - Matsui, Miki
AU - Konno, Hiroyuki
AU - Doh-ura, Katsumi
N1 - Funding Information:
We thank Y. Fujiwara, A. Oguma, and K. Nishizawa for technical assistance, and T. Kitamoto and S. Mohri for discussion. We thank Animal Experimentation and Biomedical Research Core, Tohoku University Graduate School of Medicine for technical service. The authors would like to thank Enago ( www.enago.jp ) for the English language review. This work was supported by a grant from the Japan Society for the Promotion of Science (to K.T.) [grant number 15K01804 and 19K22479 ].
Publisher Copyright:
© 2022
PY - 2022/4
Y1 - 2022/4
N2 - Background: Cultured cell lines infected with prions produce an abnormal isoform of the prion protein (PrPSc). In this study, two types of cells persistently infected with prion were treated with curcumin-related compounds. We found that the compounds behave differently in neuroblastoma neuro-2a (N2a) cells infected with different prion strains. Methods: Curcumin and related compounds were applied to the two types of persistently prion infected cells to analyze the different activities of the compounds. Results: In ScN2a cells, which were infected with the Rocky Mountain Laboratory prion strain, two of the six compounds significantly reduced the PrPSc level in a dose-dependent manner. On the other hand, in N167 cells, effective suppression of the total amount of PrPSc was not observed; instead, two other compounds promoted the formation of covalently linked PrPSc dimers. Conclusions: Chemometric analysis was used to determine the factors that contributed to the different effects of the six compounds. It showed that the ability to form hydrogen bonds, such as phenolic hydroxyl groups, and hydrophobic molecular properties predominantly contributed to the reduction of the PrPSc level in the ScN2a cells and the dimer formation of PrPSc in the N167 cells, respectively. General significance: The extracted information can be used to delineate the differences among prion strains and to design compounds that are directed toward their respective activities.
AB - Background: Cultured cell lines infected with prions produce an abnormal isoform of the prion protein (PrPSc). In this study, two types of cells persistently infected with prion were treated with curcumin-related compounds. We found that the compounds behave differently in neuroblastoma neuro-2a (N2a) cells infected with different prion strains. Methods: Curcumin and related compounds were applied to the two types of persistently prion infected cells to analyze the different activities of the compounds. Results: In ScN2a cells, which were infected with the Rocky Mountain Laboratory prion strain, two of the six compounds significantly reduced the PrPSc level in a dose-dependent manner. On the other hand, in N167 cells, effective suppression of the total amount of PrPSc was not observed; instead, two other compounds promoted the formation of covalently linked PrPSc dimers. Conclusions: Chemometric analysis was used to determine the factors that contributed to the different effects of the six compounds. It showed that the ability to form hydrogen bonds, such as phenolic hydroxyl groups, and hydrophobic molecular properties predominantly contributed to the reduction of the PrPSc level in the ScN2a cells and the dimer formation of PrPSc in the N167 cells, respectively. General significance: The extracted information can be used to delineate the differences among prion strains and to design compounds that are directed toward their respective activities.
KW - Anti-prion
KW - Curcumin
KW - Partial least squares
KW - Prion
KW - Protein cross-linking
UR - http://www.scopus.com/inward/record.url?scp=85123080948&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85123080948&partnerID=8YFLogxK
U2 - 10.1016/j.bbagen.2022.130094
DO - 10.1016/j.bbagen.2022.130094
M3 - Article
C2 - 35065183
AN - SCOPUS:85123080948
SN - 0006-3002
VL - 1866
JO - Biochimica et Biophysica Acta - General Subjects
JF - Biochimica et Biophysica Acta - General Subjects
IS - 4
M1 - 130094
ER -