TY - JOUR
T1 - Magnolol and honokiol enhance HL-60 human leukemia cell differentiation induced by 1,25-dihydroxyvitamin D 3 and retinoic acid
AU - FONG, David W F
AU - TSE, Anfernee K W
AU - Poon, Ka Hung
AU - Wang, Cheng
N1 - Funding Information:
This project is supported by grants from the City University of Hong Kong (9360045-740) and Jacobson Medical (Hong Kong) Limited.
PY - 2005/2
Y1 - 2005/2
N2 - Magnolol (MG) and honokiol (HK), two lignans showing anti-inflammatory and anti-oxidant properties and abundantly available in the medicinal plants Magnolia officinalis and M. obovata, were found to enhance HL-60 cell differentiation initiated by low doses of 1,25-dihydroxyvitamin D 3 (VD 3) and all-trans-retinoic acid (ATRA). Cells expressing membrane differentiation markers CD11b and CD14 were increased from 4% in non-treated control to 8-16% after being treated with 10-30 μM MG or HK. When added to 1 nM VD 3, MG or HK increased markers expressing cells from approximately 30% to 50-80%. When either MG or HK was added to 20 nM ATRA, only CD11b, but not CD14, expressing cells were increased from 9% to 24-70%. Under the same conditions, adding MG or HK to VD 3 or ATRA treatment further enlarged the G 0/G 1 cell population and increased the expression of p27 Kip1, a cyclin-dependent kinase inhibitor. Pharmacological studies using PD098059 (a MEK inhibitor), SB203580 (a p38 MAPK inhibitor) and SP600125 (a JNK inhibitor) suggested that the MEK pathway was important for VD 3 and ATRA-induced differentiation and also its enhancement by MG or HK, the p38 MAPK pathway had a inhibitory effect and the JNK pathway had little influence. It is evident that MG and HK are potential differentiation enhancing agents which may allow the use of low doses of VD 3 and ATRA in the treatment for acute promyelocytic leukemia.
AB - Magnolol (MG) and honokiol (HK), two lignans showing anti-inflammatory and anti-oxidant properties and abundantly available in the medicinal plants Magnolia officinalis and M. obovata, were found to enhance HL-60 cell differentiation initiated by low doses of 1,25-dihydroxyvitamin D 3 (VD 3) and all-trans-retinoic acid (ATRA). Cells expressing membrane differentiation markers CD11b and CD14 were increased from 4% in non-treated control to 8-16% after being treated with 10-30 μM MG or HK. When added to 1 nM VD 3, MG or HK increased markers expressing cells from approximately 30% to 50-80%. When either MG or HK was added to 20 nM ATRA, only CD11b, but not CD14, expressing cells were increased from 9% to 24-70%. Under the same conditions, adding MG or HK to VD 3 or ATRA treatment further enlarged the G 0/G 1 cell population and increased the expression of p27 Kip1, a cyclin-dependent kinase inhibitor. Pharmacological studies using PD098059 (a MEK inhibitor), SB203580 (a p38 MAPK inhibitor) and SP600125 (a JNK inhibitor) suggested that the MEK pathway was important for VD 3 and ATRA-induced differentiation and also its enhancement by MG or HK, the p38 MAPK pathway had a inhibitory effect and the JNK pathway had little influence. It is evident that MG and HK are potential differentiation enhancing agents which may allow the use of low doses of VD 3 and ATRA in the treatment for acute promyelocytic leukemia.
KW - 1,25-Dihydroxyvitamin D
KW - All-trans-retinoic acid
KW - Differentiation
KW - Honokiol
KW - Magnolol
UR - http://www.scopus.com/inward/record.url?scp=4944240759&partnerID=8YFLogxK
U2 - 10.1016/j.biocel.2004.05.021
DO - 10.1016/j.biocel.2004.05.021
M3 - Journal article
C2 - 15474987
AN - SCOPUS:4944240759
SN - 1357-2725
VL - 37
SP - 427
EP - 441
JO - International Journal of Biochemistry and Cell Biology
JF - International Journal of Biochemistry and Cell Biology
IS - 2
ER -