ASK1-dependent recruitment and activation of macrophages induce hair growth in skin wounds

Author:

Osaka Nao123,Takahashi Takumi4,Murakami Shiori123,Matsuzawa Atsushi123,Noguchi Takuya123,Fujiwara Takeshi3,Aburatani Hiroyuki5,Moriyama Keiji4,Takeda Kohsuke123,Ichijo Hidenori123

Affiliation:

1. Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo

2. Core Research for Evolutional Science and Technology, Japan Science and Technology Corporation,

3. Strategic Approach to Drug Discovery and Development in Pharmaceutical Sciences, Center of Excellence Program, Bunkyo-ku, Tokyo 113-0033, Japan

4. Department of Orthodontics and Dentofacial Orthopedics, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima 770-8504, Japan

5. Genome Science Division, Research Center for Advanced Science and Technology and Department, The University of Tokyo, Meguro-ku, Tokyo 153-8904, Japan

Abstract

Apoptosis signal-regulating kinase 1 (ASK1) is a member of the mitogen-activated protein 3-kinase family that activates both c-Jun NH2-terminal kinase and p38 pathways in response to inflammatory cytokines and physicochemical stress. We report that ASK1 deficiency in mice results in dramatic retardation of wounding-induced hair regrowth in skin. Oligonucleotide microarray analysis revealed that expression of several chemotactic and activating factors for macrophages, as well as several macrophage-specific marker genes, was reduced in the skin wound area of ASK1-deficient mice. Intracutaneous transplantation of cytokine-activated bone marrow-derived macrophages strongly induced hair growth in both wild-type and ASK1-deficient mice. These findings indicate that ASK1 is required for wounding-induced infiltration and activation of macrophages, which play central roles in inflammation-dependent hair regrowth in skin.

Publisher

Rockefeller University Press

Subject

Cell Biology

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