Key result
Cryptotanshinone significantly inhibited C5a- and MIP-1alpha-induced macrophage migration in a concentration-dependent manner by suppressing PI3K activation and downstream Akt and ERK1/2 phosphorylation.
Cryptotanshinone inhibits macrophage chemotaxis by negatively regulating the PI3K/Akt and ERK1/2 signaling pathways, providing mechanistic insight into its anti-inflammatory properties.
May inhibit macrophage chemotaxis in vitro; leaves open in vivo effects or clinical translation.
BACKGROUND AND PURPOSE: Cryptotanshinone, the major tanshinone isolated from Salvia miltiorrhiza Bunge, exhibits anti-inflammatory activity. However, there is no report on the effect of cryptotanshinone on recruitment of leukocytes to inflammatory sites. We therefore assessed the effects of cryptotanshinone on macrophage chemotaxis. EXPERIMENTAL APPROACH: Macrophage migration induced by complement 5a (C5a) or macrophage inflammatory protein-1alpha (MIP-1alpha) was measured in vitro. Intracellular kinase translocation and phosphorylation was assessed by Western blotting. KEY RESULTS: RAW264.7 cell migration towards C5a (1 microg ml(-1)) was significantly inhibited by cryptotanshinone (1, 3, 10 and 30 microM) in a concentration-dependent manner. Primary human macrophages stimulated by C5a were similarly inhibited. C5a-evoked migration in RAW264.7 cells was significantly suppressed by wortmannin (phosphatidylinositol 3-kinase (PI3K) inhibitor), PD98059 (MEK1/2 inhibitor) and SB203580 (p38 mitogen-activated protein kinase (MAPK) inhibitor), but not by SP600125 (c-Jun N-terminal kinase (JNK) inhibitor), suggesting that activation of PI3K, ERK1/2 and p38 MAPK signal pathways was involved in responses to C5a. Western blotting revealed that cryptotanshinone significantly inhibited PI3K-p110gamma membrane translocation and phosphorylation of Akt (PI3K downstream effector protein) and ERK1/2 induced by C5a. However, neither p38 MAPK nor JNK phosphorylation was affected by cryptotanshinone. Wortmannin significantly attenuated C5a-induced PI3K-p110gamma translocation, Akt and ERK1/2 phosphorylation. PD98059 suppressed ERK1/2 phosphorylation but failed to modify PI3K-p110gamma translocation by C5a stimulation. Furthermore, MIP-1alpha-induced cell migration and PI3K-p110gamma translocation were also inhibited by cryptotanshinone in a concentration-dependent manner. CONCLUSIONS AND IMPLICATIONS: Inhibition of macrophage migration by cryptotanshinone involved inhibition of PI3K activation with consequent reduction of phosphorylation of Akt and ERK1/2.
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Don et al. (2007) studied Inflammation (macrophage migration). Cryptotanshinone vs. Control (C5a or MIP-1alpha stimulation alone) was evaluated on Macrophage migration induced by C5a or MIP-1alpha and intracellular kinase translocation/phosphorylation. Cryptotanshinone significantly inhibited C5a- and MIP-1alpha-induced macrophage migration in a concentration-dependent manner by suppressing PI3K activation and downstream Akt and ERK1/2 phosphorylation.
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