ERK MAP kinase is required in 1,25(OH)2D3-induced differentiation in human osteoblasts

被引:18
作者
Chae, HJ
Jeong, BJ
Ha, MS
Lee, JK
Byun, JO
Jung, WY
Yun, YG
Lee, DG
Oh, S
Chae, SW
Kwak, YG
Kim, HH
Lee, ZH
Kim, HR [1 ]
机构
[1] Wonkwang Univ, Dept Dent Pharamcol, Sch Dent, Iksan 570749, Chonbuk, South Korea
[2] Wonkwang Univ, Wonkwang Dent Res Inst, Sch Dent, Iksan 570749, Chonbuk, South Korea
[3] Wonkwang Univ, Dept Maxillofacial Surg, Sch Dent, Iksan 570749, Chonbuk, South Korea
[4] Wonkwang Univ, Dept Oral Anat, Sch Dent, Iksan 570749, Chonbuk, South Korea
[5] Wonkwang Univ, Dept Oriental Prescript, Sch Dent, Iksan 570749, Chonbuk, South Korea
[6] Chosun Univ, Natl Res Lab Bone Metab, Kwangju 501759, South Korea
[7] Chosun Univ, Res Ctr Proteinous Mat, Kwangju 501759, South Korea
关键词
D O I
10.1081/IPH-120003401
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Expression of alkaline phosphatase(ALP)activity represents a key event during the differentiation processes of osteoblasts, and the level of ALP activity has been routinely used as a relative measure of differentiation stages of osteoblasts. In human osteoblasts, we showed that vitamin D-3 analogue, 1,25(OH)(2)D-3, had a stimulatory effect on ALP activity after 3 days, compared with control. The treatment of PD098059, an ERK MAP Kinase inhibitor, had a reducing effect on ALP activity, a differentiation marker in 1,25(OH)(2)D-3-treated primary human osteoblasts. However, SB203580, a potent p38 MAP Kinase inhibitor, had no effect on the differentiation in this system. This indicates that ERK, not p38, is directly related to 1,25(OH)(2)D-3-stimulated ALP activity in primary human osteoblasts. These results also show that the vitamin D-3 analogue stimulates ERK1 activation in primary human osteoblasts. This finding provides one of signaling pathways for differentiation in primary human osteoblasts.
引用
收藏
页码:31 / 41
页数:11
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