TY - JOUR
T1 - Comparison of the activities of various alginates to induce TNF-α secretion in RAW264.7 cells
AU - Kurachi, Maki
AU - Nakashima, Takuji
AU - Miyajima, Chihiro
AU - Iwamoto, Yoshiko
AU - Muramatsu, Tsuyoshi
AU - Yamaguchi, Kenichi
AU - Oda, Tatsuya
PY - 2005/9
Y1 - 2005/9
N2 - We compared the abilities of alginate polymers having different molecular sizes and compositions to induce the secretion of tumor necrosis factor (TNF)-α in RAW264.7 cells. The molecular sizes and α-L-guluronate/ β-D-mannuronate (M/G) ratios of highly purified alginate polymers used in this study were 9000-38∈000 and 1.50-3.17, respectively. Among the alginates tested, I-S, which had the highest molecular weight, showed the most potent TNF-α-inducing activity. The M/G ratio also seemed to influence this activity, and, among alginates with similar molecular sizes, alginates with a higher M/G ratio tended to show higher activity. Interestingly, the enzymatic depolymerization of I-S with bacterial alginate lyase resulted in a dramatic increase in the TNF-α-inducing activity. Such an effect of enzymatic digestion was also observed in a relatively low-molecular-weight alginate (ULV-3), which originally had very low TNF-α-inducing activity. Furthermore, the inhibition profiles of the TNF-α-inducing activity of enzymatically digested I-S shown by three specific mitogen-activated protein (MAP) kinase inhibitors differed from those of intact I-S. These results suggest that the underlying mechanism of the TNF-α-inducing activity of enzymatically depolymerized alginate oligomers is not necessarily the same as that of original alginate polymer.
AB - We compared the abilities of alginate polymers having different molecular sizes and compositions to induce the secretion of tumor necrosis factor (TNF)-α in RAW264.7 cells. The molecular sizes and α-L-guluronate/ β-D-mannuronate (M/G) ratios of highly purified alginate polymers used in this study were 9000-38∈000 and 1.50-3.17, respectively. Among the alginates tested, I-S, which had the highest molecular weight, showed the most potent TNF-α-inducing activity. The M/G ratio also seemed to influence this activity, and, among alginates with similar molecular sizes, alginates with a higher M/G ratio tended to show higher activity. Interestingly, the enzymatic depolymerization of I-S with bacterial alginate lyase resulted in a dramatic increase in the TNF-α-inducing activity. Such an effect of enzymatic digestion was also observed in a relatively low-molecular-weight alginate (ULV-3), which originally had very low TNF-α-inducing activity. Furthermore, the inhibition profiles of the TNF-α-inducing activity of enzymatically digested I-S shown by three specific mitogen-activated protein (MAP) kinase inhibitors differed from those of intact I-S. These results suggest that the underlying mechanism of the TNF-α-inducing activity of enzymatically depolymerized alginate oligomers is not necessarily the same as that of original alginate polymer.
KW - Alginate
KW - Alginate lyase
KW - Macrophage
KW - RAW264.7 cells
KW - TNF-α
UR - http://www.scopus.com/inward/record.url?scp=24044472011&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=24044472011&partnerID=8YFLogxK
U2 - 10.1007/s10156-005-0392-0
DO - 10.1007/s10156-005-0392-0
M3 - Article
C2 - 16133713
AN - SCOPUS:24044472011
SN - 1341-321X
VL - 11
SP - 199
EP - 203
JO - Journal of Infection and Chemotherapy
JF - Journal of Infection and Chemotherapy
IS - 4
ER -