Salsolinol Damaged Neuroblastoma SH-SY5Y Cells Induce Proliferation of Human Monocyte THP-1 Cells Through the mTOR Pathway in a Co-culture System

Fuli Wang, Junjun Ni, Xianghan Wang, Bingjie Xie, Chengcheng Feng, Sibo Zhao, Yasmeem Saeed, Hong Qing, Yulin Deng

Research output: Contribution to journalArticle

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Abstract

Despite extensive efforts to study the inflammatory process in the central nervous system of Parkinson's disease (PD) patients, little is known about the role of peripheral blood mononuclear cells (PBMCs) in PD. In the present study, we used an in vitro co-culture system to study the role of the human monocyte cell line THP-1 in medium conditioned by the neuroblastoma cell line SH-SY5Y damaged with the endogenous neurotoxin 1-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline (Salsolinol, Sal) in co-culture with the human glioma cell line U87. For this purpose, SH-SY5Y and U87 co-cultures were treated with Sal, and this conditioned medium containing mediators, including the potential effector CCL2, was isolated and applied to THP-1 cells. This treatment resulted in approximately 19 % cell proliferation as well as activation of mTOR and induction of phosphorylated 4E-BP1, S6K1, PI3K, and AKT proteins. Treatment with rapamycin, an mTOR inhibitor, attenuated the proliferation of THP-1 cells. U87 glial cells were essential for this as medium conditioned without them had no effect on THP-1 cells. These results suggest a positive effect of THP-1 cells on Sal-induced neurotoxicity in a cellular model of PD and this is likely mediated by the enhancement of cell proliferation through activation of the mTOR signaling pathway. Hence, PBMCs and their mTOR signaling pathway could be of therapeutic benefit in treating the endogenous neurotoxin-induced neuroinflammation in PD.

Original languageEnglish
Pages (from-to)932-41
Number of pages10
JournalNeurochemical Research
Volume40
Issue number5
DOIs
Publication statusPublished - May 2015

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Cell proliferation
Coculture Techniques
Neuroblastoma
Parkinson Disease
Monocytes
Conditioned Culture Medium
Cell Proliferation
Cells
Neurotoxins
Cell Line
Blood Cells
Blood
Chemical activation
Central Nervous System Diseases
Neurology
Sirolimus
Phosphatidylinositol 3-Kinases
Cell culture
Glioma
Neuroglia

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Salsolinol Damaged Neuroblastoma SH-SY5Y Cells Induce Proliferation of Human Monocyte THP-1 Cells Through the mTOR Pathway in a Co-culture System. / Wang, Fuli; Ni, Junjun; Wang, Xianghan; Xie, Bingjie; Feng, Chengcheng; Zhao, Sibo; Saeed, Yasmeem; Qing, Hong; Deng, Yulin.

In: Neurochemical Research, Vol. 40, No. 5, 05.2015, p. 932-41.

Research output: Contribution to journalArticle

Wang, Fuli ; Ni, Junjun ; Wang, Xianghan ; Xie, Bingjie ; Feng, Chengcheng ; Zhao, Sibo ; Saeed, Yasmeem ; Qing, Hong ; Deng, Yulin. / Salsolinol Damaged Neuroblastoma SH-SY5Y Cells Induce Proliferation of Human Monocyte THP-1 Cells Through the mTOR Pathway in a Co-culture System. In: Neurochemical Research. 2015 ; Vol. 40, No. 5. pp. 932-41.
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abstract = "Despite extensive efforts to study the inflammatory process in the central nervous system of Parkinson's disease (PD) patients, little is known about the role of peripheral blood mononuclear cells (PBMCs) in PD. In the present study, we used an in vitro co-culture system to study the role of the human monocyte cell line THP-1 in medium conditioned by the neuroblastoma cell line SH-SY5Y damaged with the endogenous neurotoxin 1-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline (Salsolinol, Sal) in co-culture with the human glioma cell line U87. For this purpose, SH-SY5Y and U87 co-cultures were treated with Sal, and this conditioned medium containing mediators, including the potential effector CCL2, was isolated and applied to THP-1 cells. This treatment resulted in approximately 19 {\%} cell proliferation as well as activation of mTOR and induction of phosphorylated 4E-BP1, S6K1, PI3K, and AKT proteins. Treatment with rapamycin, an mTOR inhibitor, attenuated the proliferation of THP-1 cells. U87 glial cells were essential for this as medium conditioned without them had no effect on THP-1 cells. These results suggest a positive effect of THP-1 cells on Sal-induced neurotoxicity in a cellular model of PD and this is likely mediated by the enhancement of cell proliferation through activation of the mTOR signaling pathway. Hence, PBMCs and their mTOR signaling pathway could be of therapeutic benefit in treating the endogenous neurotoxin-induced neuroinflammation in PD.",
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AU - Saeed, Yasmeem

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