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The DOI matches its Crossref record; 124 of the 124 references it cites were found in a registry or an index.

Cellular and molecular basis for the regulation of inflammation by TGF-

Open access
Yoshimura, A., Wakabayashi, Y., Mori, T.·2010·Journal of Biochemistry

Abstract

Transforming growth factor-beta (TGF-beta) has been shown to play an essential role in the suppression of inflammation, yet recent studies have revealed the positive roles of TGF-beta in inflammatory responses. For example, TGF-beta induces Foxp3-positive regulatory T cells (iTregs) in the presence of interleukin-2 (IL-2), while in the presence of IL-6, it induces pathogenic IL-17 producing Th17 cells. TGF-beta inhibits the proliferation of immune cells as well as cytokine production via Foxp3-dependent and -independent mechanisms. Little is known about molecular mechanisms involved in immune suppression via TGF-beta; however, Smad2/3 have been shown to play essential roles in Foxp3 induction as well as in IL-2 and IFN-gamma suppression, whereas Th17 differentiation is promoted via the Smad-independent pathway. Interaction between TGF-beta and other cytokine signaling is important in establishing the balance of immunity and tolerance.

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Metadata

Authors
Yoshimura, A., Wakabayashi, Y., & Mori, T.
Venue
Journal of Biochemistry
Published
2010-04-20
Volume
147
Issue
6
Pages
781-792
ISSN
0021-924X (ISSN-L)
OpenAlex
W2161112755
Cited by
391
References
124
FWCI
11.22
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Cellular and molecular basis for the regulation of inflammation by TGF-. https://app.cochat.ai/papers/10.1093/jb/mvq043
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Yoshimura, A., Wakabayashi, Y., & Mori, T. (2010). Cellular and molecular basis for the regulation of inflammation by TGF-. Journal of Biochemistry. https://doi.org/10.1093/jb/mvq043

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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