The Ccl17 gene encoding TARC is synergistically transactivated by PU.1 and IRF4 driven by the mammalian common promoter in dendritic cells

Naoto Ito; Fumiya Sakata; Masakazu Hachisu; Kazuki Nagata; Tomoka Ito; Kurumi Nomura; Masanori Nagaoka; Keito Inaba; Mutsuko Hara; Nobuhiro Nakano; Tadaaki Nakajima; Takuya Yashiro; Chiharu Nishiyama

doi:10.1111/all.15184

The Ccl17 gene encoding TARC is synergistically transactivated by PU.1 and IRF4 driven by the mammalian common promoter in dendritic cells

Naoto Ito, Fumiya Sakata, Masakazu Hachisu, Kazuki Nagata, Tomoka Ito, Kurumi Nomura, Masanori Nagaoka, Keito Inaba, Mutsuko Hara, Nobuhiro Nakano, Tadaaki Nakajima, Takuya Yashiro, Chiharu Nishiyama

Department of Biological Science and Technology

Research output: Contribution to journal › Letter › peer-review

4 Citations (Scopus)

Original language	English
Pages (from-to)	1054-1059
Number of pages	6
Journal	Allergy: European Journal of Allergy and Clinical Immunology
Volume	77
Issue number	3
DOIs	https://doi.org/10.1111/all.15184
Publication status	Published - Mar 2022

Keywords

CCL17
IRF4
PU.1
TARC
dendritic cells

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10.1111/all.15184

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Ito, N., Sakata, F., Hachisu, M., Nagata, K., Ito, T., Nomura, K., Nagaoka, M., Inaba, K., Hara, M., Nakano, N., Nakajima, T., Yashiro, T., & Nishiyama, C. (2022). The Ccl17 gene encoding TARC is synergistically transactivated by PU.1 and IRF4 driven by the mammalian common promoter in dendritic cells. Allergy: European Journal of Allergy and Clinical Immunology, 77(3), 1054-1059. https://doi.org/10.1111/all.15184

@article{ff59d2fa32fb4851aaa1c8a99090545b,

title = "The Ccl17 gene encoding TARC is synergistically transactivated by PU.1 and IRF4 driven by the mammalian common promoter in dendritic cells",

keywords = "CCL17, IRF4, PU.1, TARC, dendritic cells",

author = "Naoto Ito and Fumiya Sakata and Masakazu Hachisu and Kazuki Nagata and Tomoka Ito and Kurumi Nomura and Masanori Nagaoka and Keito Inaba and Mutsuko Hara and Nobuhiro Nakano and Tadaaki Nakajima and Takuya Yashiro and Chiharu Nishiyama",

note = "Funding Information: This work was supported by a Grant‐in‐Aid for Scientific Research (B) (20H02939 to CN), Grant‐in‐Aid for Scientific Research (C) (21K05297 to MH and 19K05884 to TY), a Research Fellowship for Young Scientists (DC) and Grant‐in‐Aid for JSPS Fellows 21J12113 (both to K Nagata), a Tokyo University of Science Grant for President's Research Promotion (to CN), the MEXT‐Supported Program for the Strategic Research Foundation at Private Universities (Translational Research Center, Tokyo University of Science), the Tojuro Iijima Foundation for Food Science and Technology (to CN and TY), a Research Grant from the Mishima Kaiun Memorial Foundation (to CN), and a Research Grant from Takeda Science Foundation (to CN). Funding Information: This work was supported by a Grant-in-Aid for Scientific Research (B) (20H02939 to CN), Grant-in-Aid for Scientific Research (C) (21K05297 to MH and 19K05884 to TY), a Research Fellowship for Young Scientists (DC) and Grant-in-Aid for JSPS Fellows 21J12113 (both to K Nagata), a Tokyo University of Science Grant for President's Research Promotion (to CN), the MEXT-Supported Program for the Strategic Research Foundation at Private Universities (Translational Research Center, Tokyo University of Science), the Tojuro Iijima Foundation for Food Science and Technology (to CN and TY), a Research Grant from the Mishima Kaiun Memorial Foundation (to CN), and a Research Grant from Takeda Science Foundation (to CN). We thank the members of the Laboratory of Molecular Biology and Immunology, Department of Biological Science and Technology, Tokyo University of Science for constructive discussions and technical support. This work was supported by a Grant-in-Aid for Scientific Research (B) 20H02939 (CN), Grant-in-Aid for Scientific Research (C) 21K05297 (MH) and 19K05884 (TY); a Research Fellowship for Young Scientists DC2 and Grant-in-Aid for JSPS Fellows 21J12113 (K Nagata); a Tokyo University of Science Grant for President?s Research Promotion (CN); the MEXT-Supported Program for the Strategic Research Foundation at Private Universities (Translational Research Center, Tokyo University of Science); the Tojuro Iijima Foundation for Food Science and Technology (CN and TY); and a Research Grant from the Mishima Kaiun Memorial Foundation (CN). Funding Information: We thank the members of the Laboratory of Molecular Biology and Immunology, Department of Biological Science and Technology, Tokyo University of Science for constructive discussions and technical support. This work was supported by a Grant‐in‐Aid for Scientific Research (B) 20H02939 (CN), Grant‐in‐Aid for Scientific Research (C) 21K05297 (MH) and 19K05884 (TY); a Research Fellowship for Young Scientists DC2 and Grant‐in‐Aid for JSPS Fellows 21J12113 (K Nagata); a Tokyo University of Science Grant for President{\textquoteright}s Research Promotion (CN); the MEXT‐Supported Program for the Strategic Research Foundation at Private Universities (Translational Research Center, Tokyo University of Science); the Tojuro Iijima Foundation for Food Science and Technology (CN and TY); and a Research Grant from the Mishima Kaiun Memorial Foundation (CN). ",

year = "2022",

month = mar,

doi = "10.1111/all.15184",

language = "English",

volume = "77",

pages = "1054--1059",

journal = "Allergy: European Journal of Allergy and Clinical Immunology",

issn = "0105-4538",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "3",

}

Ito, N, Sakata, F, Hachisu, M, Nagata, K, Ito, T, Nomura, K, Nagaoka, M, Inaba, K, Hara, M, Nakano, N, Nakajima, T, Yashiro, T & Nishiyama, C 2022, 'The Ccl17 gene encoding TARC is synergistically transactivated by PU.1 and IRF4 driven by the mammalian common promoter in dendritic cells', Allergy: European Journal of Allergy and Clinical Immunology, vol. 77, no. 3, pp. 1054-1059. https://doi.org/10.1111/all.15184

TY - JOUR

T1 - The Ccl17 gene encoding TARC is synergistically transactivated by PU.1 and IRF4 driven by the mammalian common promoter in dendritic cells

AU - Ito, Naoto

AU - Sakata, Fumiya

AU - Hachisu, Masakazu

AU - Nagata, Kazuki

AU - Ito, Tomoka

AU - Nomura, Kurumi

AU - Nagaoka, Masanori

AU - Inaba, Keito

AU - Hara, Mutsuko

AU - Nakano, Nobuhiro

AU - Nakajima, Tadaaki

AU - Yashiro, Takuya

AU - Nishiyama, Chiharu

N1 - Funding Information: This work was supported by a Grant‐in‐Aid for Scientific Research (B) (20H02939 to CN), Grant‐in‐Aid for Scientific Research (C) (21K05297 to MH and 19K05884 to TY), a Research Fellowship for Young Scientists (DC) and Grant‐in‐Aid for JSPS Fellows 21J12113 (both to K Nagata), a Tokyo University of Science Grant for President's Research Promotion (to CN), the MEXT‐Supported Program for the Strategic Research Foundation at Private Universities (Translational Research Center, Tokyo University of Science), the Tojuro Iijima Foundation for Food Science and Technology (to CN and TY), a Research Grant from the Mishima Kaiun Memorial Foundation (to CN), and a Research Grant from Takeda Science Foundation (to CN). Funding Information: This work was supported by a Grant-in-Aid for Scientific Research (B) (20H02939 to CN), Grant-in-Aid for Scientific Research (C) (21K05297 to MH and 19K05884 to TY), a Research Fellowship for Young Scientists (DC) and Grant-in-Aid for JSPS Fellows 21J12113 (both to K Nagata), a Tokyo University of Science Grant for President's Research Promotion (to CN), the MEXT-Supported Program for the Strategic Research Foundation at Private Universities (Translational Research Center, Tokyo University of Science), the Tojuro Iijima Foundation for Food Science and Technology (to CN and TY), a Research Grant from the Mishima Kaiun Memorial Foundation (to CN), and a Research Grant from Takeda Science Foundation (to CN). We thank the members of the Laboratory of Molecular Biology and Immunology, Department of Biological Science and Technology, Tokyo University of Science for constructive discussions and technical support. This work was supported by a Grant-in-Aid for Scientific Research (B) 20H02939 (CN), Grant-in-Aid for Scientific Research (C) 21K05297 (MH) and 19K05884 (TY); a Research Fellowship for Young Scientists DC2 and Grant-in-Aid for JSPS Fellows 21J12113 (K Nagata); a Tokyo University of Science Grant for President?s Research Promotion (CN); the MEXT-Supported Program for the Strategic Research Foundation at Private Universities (Translational Research Center, Tokyo University of Science); the Tojuro Iijima Foundation for Food Science and Technology (CN and TY); and a Research Grant from the Mishima Kaiun Memorial Foundation (CN). Funding Information: We thank the members of the Laboratory of Molecular Biology and Immunology, Department of Biological Science and Technology, Tokyo University of Science for constructive discussions and technical support. This work was supported by a Grant‐in‐Aid for Scientific Research (B) 20H02939 (CN), Grant‐in‐Aid for Scientific Research (C) 21K05297 (MH) and 19K05884 (TY); a Research Fellowship for Young Scientists DC2 and Grant‐in‐Aid for JSPS Fellows 21J12113 (K Nagata); a Tokyo University of Science Grant for President’s Research Promotion (CN); the MEXT‐Supported Program for the Strategic Research Foundation at Private Universities (Translational Research Center, Tokyo University of Science); the Tojuro Iijima Foundation for Food Science and Technology (CN and TY); and a Research Grant from the Mishima Kaiun Memorial Foundation (CN).

PY - 2022/3

Y1 - 2022/3

KW - CCL17

KW - IRF4

KW - PU.1

KW - TARC

KW - dendritic cells

UR - http://www.scopus.com/inward/record.url?scp=85120617590&partnerID=8YFLogxK

U2 - 10.1111/all.15184

DO - 10.1111/all.15184

M3 - Letter

C2 - 34807993

AN - SCOPUS:85120617590

SN - 0105-4538

VL - 77

SP - 1054

EP - 1059

JO - Allergy: European Journal of Allergy and Clinical Immunology

JF - Allergy: European Journal of Allergy and Clinical Immunology

IS - 3

ER -

The Ccl17 gene encoding TARC is synergistically transactivated by PU.1 and IRF4 driven by the mammalian common promoter in dendritic cells

Keywords

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