The inhibitory mechanism of methylmercury on differentiation of human neuroblastorna cells
- Authors
- Kim, Youn-Jung; Kim, Young-Seok; Kim, Mi-Soon; Ryu, Jae-Chun
- Issue Date
- 2007-05-05
- Publisher
- ELSEVIER IRELAND LTD
- Citation
- TOXICOLOGY, v.234, no.1-2, pp.1 - 9
- Abstract
- Methylmercury (MeHg) is a ubiquitous environmental toxicant and shows neurotoxicity to central nerve system (CNS) or neuronal cells. It has been known that MeHg has more influence to developing or differentiating CNS/neuronal cells than adult or differentiated CNS/neuronal cells. This study examined the effect of MeHg on differentiation of human neuroblastoma SH-SY5Y cells induced by all-trans-retinoic acid (RA). MeHg caused the impairment of the RA-induced G(1/0) phase arrest; it was induced the reduction of G(1/0) phase and S phase arrest. Extracellular signal-regulated kinase 1/2 (ERK1/2) and protein kinase C (PKC) are involved in the RA-mediated differentiation and cell cycle progression. Activation of ERK1/2 by RA was increased more in MeHg-treated differentiating cells, comparing with only RA-treated groups. Furthermore, in both cases of inhibition of ERK1/2 with PD98059 or inhibition of PKC with GF109203X, RA/MeHg-induced ERK1/2 phosphorylation was reduced and G(1/0) phase arrest was induced. Thus, it indicates that the neuronal differentiation with RA was mediated by the ERK1/2 and PKC related pathway and MeHg resulted in neurotoxic influences through the disturbance in steps of differentiation by this pathway. These results suggest that MeHg inhibits RA-induced differentiation in SH-SY5Y cells by a pathway dependent ERK1/2 and PKC. (C) 2007 Elsevier Ireland Ltd. All rights reserved.
- Keywords
- PROTEIN-KINASE-C; NEURITE OUTGROWTH; MAP KINASE; RETINOIC ACID; SUSTAINED ACTIVATION; NERVOUS-SYSTEM; GROWTH-FACTOR; HEAVY-METALS; PC12 CELLS; IN-VITRO; PROTEIN-KINASE-C; NEURITE OUTGROWTH; MAP KINASE; RETINOIC ACID; SUSTAINED ACTIVATION; NERVOUS-SYSTEM; GROWTH-FACTOR; HEAVY-METALS; PC12 CELLS; IN-VITRO; methylmercury; differentiation; cell cycle; retinoic acid; ERK; PKC
- ISSN
- 0300-483X
- URI
- https://pubs.kist.re.kr/handle/201004/134398
- DOI
- 10.1016/j.tox.2007.01.003
- Appears in Collections:
- KIST Article > 2007
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