dc.contributor.author | Tu H | |
dc.contributor.author | Gullberg D | |
dc.contributor.author | Anbazhagan P | |
dc.contributor.author | Koivunen J | |
dc.contributor.author | Juffer AH | |
dc.contributor.author | Saarakkala S | |
dc.contributor.author | Heino J | |
dc.contributor.author | Finnila MA | |
dc.contributor.author | Lu N | |
dc.contributor.author | Pihlajaniemi T | |
dc.contributor.author | Heikkinen A | |
dc.contributor.author | Kemppainen A | |
dc.contributor.author | Kapyla J | |
dc.date.accessioned | 2022-10-28T12:46:19Z | |
dc.date.available | 2022-10-28T12:46:19Z | |
dc.identifier.uri | https://www.utupub.fi/handle/10024/161940 | |
dc.description.abstract | 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 alpha 11 beta 1 is a collagen receptor known to recognize the GFOGER (O=hydroxyproline) sequence in collagens. Interestingly, collagen XIII and integrin alpha 11 beta 1 both have a role in the regulation of bone homeostasis. To study whether alpha 11 beta 1 is a receptor for collagen XIII, we utilized C2C12 cells transfected to express alpha 11 beta 1 as their only collagen receptor. The interaction between collagen XIII and integrin alpha 11 beta 1 was also confirmed by surface plasmon resonance and pull-down assays. We discovered that integrin alpha 11 beta 1 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 alpha 11-I domain. Furthermore, we studied the in vivo significance of the alpha 11 beta 1-collagen XIII interaction by crossbreeding alpha 11 null mice (Itga11(-/-)) with mice overexpressing Col13a1 (Col13a1(oe)). When we evaluated the bone morphology by microcomputed tomography, Col13a1(oe) 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 alpha 11 beta 1 as a new collagen XIII receptor and demonstrates that this ligand-receptor pair has a role in the maintenance of bone homeostasis. | |
dc.language.iso | en | |
dc.publisher | SPRINGER | |
dc.title | Integrin alpha 11 beta 1 is a receptor for collagen XIII | |
dc.identifier.url | https://doi.org/10.1007/s00441-020-03300-y | |
dc.identifier.urn | URN:NBN:fi-fe2021042825833 | |
dc.contributor.organization | fi=PÄÄT Biokemia|en=PÄÄT Biochemistry| | |
dc.contributor.organization | fi=BioCity Turku|en=BioCity Turku| | |
dc.contributor.organization | fi=MediCity|en=MediCity Research Laboratory| | |
dc.contributor.organization-code | 2606201 | |
dc.contributor.organization-code | 2609260 | |
dc.converis.publication-id | 51359214 | |
dc.converis.url | https://research.utu.fi/converis/portal/Publication/51359214 | |
dc.identifier.eissn | 1432-0878 | |
dc.identifier.jour-issn | 0302-766X | |
dc.okm.affiliatedauthor | Dataimport, MediCity | |
dc.okm.affiliatedauthor | Heino, Jyrki | |
dc.okm.affiliatedauthor | Käpylä, Jarmo | |
dc.okm.discipline | 1182 Biokemia, solu- ja molekyylibiologia | fi_FI |
dc.okm.discipline | 1182 Biochemistry, cell and molecular biology | en_GB |
dc.okm.internationalcopublication | international co-publication | |
dc.okm.internationality | International publication | |
dc.okm.type | Journal article | |
dc.publisher.country | Germany | en_GB |
dc.publisher.country | Saksa | fi_FI |
dc.publisher.country-code | DE | |
dc.relation.doi | 10.1007/s00441-020-03300-y | |
dc.relation.ispartofjournal | Cell and Tissue Research | |
dc.year.issued | 2020 | |