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On the use of abiotic sialic acids to attenuate cell inflammation.


ABSTRACT: Sialic acid (Sia) residues on cell surface are critical for myriad cellular events such as immunity and inflammation. We herein reported the use of abiotic Sia to raise the thresholds of inflammatory cell responses. Identified from a panel of structurally diversified Sia analogs via a cell inflammation assay, Sia-2, with N-butyryl moiety at C-5, markedly lowered LPS-stimulated NF-?B activity in macrophages. Further analysis shows that Sia-2 attenuates phosphorylation of I?B and Erk1/2/p38/JNK, critical for NF-?B signaling and MAPK signaling, and lowers gene transcription of proinflammatory interleukin-6. These results support the use of abiotic Sia as promising agents to modulate cell surface Sia-pertinent cell signaling.

SUBMITTER: Xue Z 

PROVIDER: S-EPMC6251910 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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On the use of abiotic sialic acids to attenuate cell inflammation.

Xue Zhongwei Z   Zhao Hu H   Zhu Rui R   Chen Congcong C   Cao Hongzhi H   Han Jiahuai J   Han Shoufa S  

Scientific reports 20181123 1


Sialic acid (Sia) residues on cell surface are critical for myriad cellular events such as immunity and inflammation. We herein reported the use of abiotic Sia to raise the thresholds of inflammatory cell responses. Identified from a panel of structurally diversified Sia analogs via a cell inflammation assay, Sia-2, with N-butyryl moiety at C-5, markedly lowered LPS-stimulated NF-κB activity in macrophages. Further analysis shows that Sia-2 attenuates phosphorylation of IκB and Erk1/2/p38/JNK, c  ...[more]

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