TY - JOUR
T1 - Characterization of cellular uptake and distribution of coenzyme Q10 and vitamin E in PC12 cells
AU - Saito, Yoshiro
AU - Fukuhara, Akiko
AU - Nishio, Keiko
AU - Hayakawa, Mieko
AU - Ogawa, Yoko
AU - Sakamoto, Hirokazu
AU - Fujii, Kenji
AU - Yoshida, Yasukazu
AU - Niki, Etsuo
N1 - Funding Information:
This study was supported by Grants-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (18790081 and 19300256).
PY - 2009/5
Y1 - 2009/5
N2 - Coenzyme Q (CoQ) is a well-known electron transporter in the mitochondrial respiratory chain. Furthermore, ubiquinol (UQH2) - a reduced form of ubiquinone (UQ) - has been shown to act as a radical-scavenging antioxidant. Some studies have reported the beneficial effect of CoQ addition to cultured cells; however, the cellular uptake and distribution of CoQ have not been elucidated. In the present study, we used rat pheochromocytoma PC12 cells to investigate and compare the cellular uptake and distribution of CoQ10 and α-tocopherol (αT). UQ10 or UQ10H2 treatment resulted in an increase in the cellular content of both CoQ10 in a time- and concentration-dependent manner. A subcellular fractionation study revealed that the added UQ10 as well as UQ10H2 mainly localized in the mitochondrial fraction, which is similar to the localization of endogenous CoQ but different from that of αT. The cellular distribution of αT directly corresponded to the lipid distribution, while the CoQ distribution did not show any relationship with the lipid distribution, particularly in the mitochondrial and microsomal fractions. These results indicate that the cellular distribution of CoQ is completely different from that of αT; moreover, a certain system which accumulates CoQ preferentially in mitochondria may be suggested.
AB - Coenzyme Q (CoQ) is a well-known electron transporter in the mitochondrial respiratory chain. Furthermore, ubiquinol (UQH2) - a reduced form of ubiquinone (UQ) - has been shown to act as a radical-scavenging antioxidant. Some studies have reported the beneficial effect of CoQ addition to cultured cells; however, the cellular uptake and distribution of CoQ have not been elucidated. In the present study, we used rat pheochromocytoma PC12 cells to investigate and compare the cellular uptake and distribution of CoQ10 and α-tocopherol (αT). UQ10 or UQ10H2 treatment resulted in an increase in the cellular content of both CoQ10 in a time- and concentration-dependent manner. A subcellular fractionation study revealed that the added UQ10 as well as UQ10H2 mainly localized in the mitochondrial fraction, which is similar to the localization of endogenous CoQ but different from that of αT. The cellular distribution of αT directly corresponded to the lipid distribution, while the CoQ distribution did not show any relationship with the lipid distribution, particularly in the mitochondrial and microsomal fractions. These results indicate that the cellular distribution of CoQ is completely different from that of αT; moreover, a certain system which accumulates CoQ preferentially in mitochondria may be suggested.
KW - Cellular distribution
KW - Cellular uptake
KW - Coenzyme Q
KW - Subcellular fractionation study
KW - Vitamin E
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U2 - 10.1016/j.jnutbio.2008.04.005
DO - 10.1016/j.jnutbio.2008.04.005
M3 - Article
C2 - 18602819
AN - SCOPUS:63249110681
SN - 0955-2863
VL - 20
SP - 350
EP - 357
JO - Journal of Nutritional Biochemistry
JF - Journal of Nutritional Biochemistry
IS - 5
ER -