Integrin α11β1 is a receptor for collagen XIII.
Jarkko KoivunenHongmin TuAntti KemppainenPadmanabhan AnbazhaganMikko A FinniläSimo SaarakkalaJarmo KäpyläNing LuAnne HeikkinenAndré H JufferJyrki HeinoDonald GullbergTaina PihlajaniemiPublished in: Cell and tissue research (2020)
Collagen XIII is a conserved transmembrane collagen mainly expressed in mesenchymal tissues. Previously, we have shown that collagen XIII modulates tissue development and homeostasis. Integrins are a family of receptors that mediate signals from the environment into the cells and vice versa. Integrin α11β1 is a collagen receptor known to recognize the GFOGER (O=hydroxyproline) sequence in collagens. Interestingly, collagen XIII and integrin α11β1 both have a role in the regulation of bone homeostasis. To study whether α11β1 is a receptor for collagen XIII, we utilized C2C12 cells transfected to express α11β1 as their only collagen receptor. The interaction between collagen XIII and integrin α11β1 was also confirmed by surface plasmon resonance and pull-down assays. We discovered that integrin α11β1 mediates cell adhesion to two collagenous motifs, namely GPKGER and GF(S)QGEK, that were shown to act as the recognition sites for the integrin α11-I domain. Furthermore, we studied the in vivo significance of the α11β1-collagen XIII interaction by crossbreeding α11 null mice (Itga11-/-) with mice overexpressing Col13a1 (Col13a1oe). When we evaluated the bone morphology by microcomputed tomography, Col13a1oe mice had a drastic bone overgrowth followed by severe osteoporosis, whereas the double mutant mouse line showed a much milder bone phenotype. To conclude, our data identifies integrin α11β1 as a new collagen XIII receptor and demonstrates that this ligand-receptor pair has a role in the maintenance of bone homeostasis.
Keyphrases
- cell adhesion
- wound healing
- bone mineral density
- tissue engineering
- induced apoptosis
- gene expression
- cell migration
- soft tissue
- bone loss
- adipose tissue
- bone marrow
- high fat diet induced
- cell cycle arrest
- binding protein
- cell death
- body composition
- metabolic syndrome
- cell proliferation
- transcription factor
- electronic health record
- single cell
- drug induced
- amino acid