Abstract |
Extracellular matrix (ECM) underlies a complicated multicellular architecture that is subjected to significant forces from mechanical environment. Although various components of the ECM have been enumerated, mechanisms that evolve the sophisticated ECM architecture remain to be addressed. Here we show that periostin, a matricellular protein, promotes incorporation of tenascin-C into the ECM and organizes a meshwork architecture of the ECM. We found that both periostin null mice and tenascin-C null mice exhibited a similar phenotype, confined tibial periostitis, which possibly corresponds to medial tibial stress syndrome in human sports injuries. Periostin possessed adjacent domains that bind to tenascin-C and the other ECM protein: fibronectin and type I collagen, respectively. These adjacent domains functioned as a bridge between tenascin-C and the ECM, which increased deposition of tenascin-C on the ECM. The deposition of hexabrachions of tenascin-C may stabilize bifurcations of the ECM fibrils, which is integrated into the extracellular meshwork architecture. This study suggests a role for periostin in adaptation of the ECM architecture in the mechanical environment.
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Authors | Isao Kii, Takashi Nishiyama, Minqi Li, Ken-Ichi Matsumoto, Mitsuru Saito, Norio Amizuka, Akira Kudo |
Journal | The Journal of biological chemistry
(J Biol Chem)
Vol. 285
Issue 3
Pg. 2028-39
(Jan 15 2010)
ISSN: 1083-351X [Electronic] United States |
PMID | 19887451
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cell Adhesion Molecules
- Fibronectins
- Postn protein, mouse
- Tenascin
- fas Receptor
- Collagen
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Topics |
- Amino Acid Sequence
- Animals
- Athletic Injuries
(metabolism, pathology)
- Cell Adhesion Molecules
(chemistry, metabolism)
- Cell Line
- Collagen
(metabolism)
- Extracellular Matrix
(chemistry, metabolism)
- Fibronectins
(metabolism)
- Humans
- Mice
- Molecular Sequence Data
- Periosteum
(metabolism, pathology)
- Periostitis
(metabolism)
- Protein Structure, Tertiary
(genetics)
- Tandem Repeat Sequences
- Tenascin
(metabolism)
- Tibia
(pathology)
- fas Receptor
(chemistry)
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