Literature DB >> 16413178

Ligand-binding specificities of laminin-binding integrins: a comprehensive survey of laminin-integrin interactions using recombinant alpha3beta1, alpha6beta1, alpha7beta1 and alpha6beta4 integrins.

Ryoko Nishiuchi1, Junichi Takagi, Maria Hayashi, Hiroyuki Ido, Yoshiko Yagi, Noriko Sanzen, Tsutomu Tsuji, Masashi Yamada, Kiyotoshi Sekiguchi.   

Abstract

The interactions of cells with basement membranes are primarily mediated via the engagement of laminins by a group of integrin family proteins, including integrins alpha3beta1, alpha6beta1, alpha7beta1 and alpha6beta4. To explore the ligand-binding specificities of these laminin-binding integrins, we produced these integrins, including two alpha7beta1 splice variants (alpha7X1beta1 and alpha7X2beta1), as soluble recombinant proteins and determined their binding specificities and affinities toward a panel of purified laminin isoforms containing distinct alpha chains. Among the five laminin-binding integrins investigated, alpha3beta1 and alpha6beta4 exhibited a clear specificity for laminin-332 (alpha3beta3gamma2) and laminin-511 (alpha5beta1gamma1)/521 (alpha5beta2gamma1), while integrin alpha6beta1 showed a broad specificity, binding to all laminin isoforms with a preference for laminin-111 (alpha1beta1gamma1), laminin-332 and laminin-511/521. The two alpha7beta1 variants were distinct from alpha3beta1, alpha6beta1 and alpha6beta4 in that they did not bind to laminin-332. alpha7X1beta1 bound to all laminins, except laminin-332, with a preference for laminin-211 (alpha2beta1gamma1)/221 (alpha2beta2gamma1) and laminin-511/521, while alpha7X2beta1 bound preferentially to laminin-111 and laminin-211/221. Laminin-511/521 was the most preferred ligand for all the laminin-binding integrins, except for alpha7X2beta1, whereas laminin-411 was the poorest ligand, capable of binding to alpha6beta1 and alpha7X1beta1 with only modest binding affinities. These comprehensive analyses of the interactions between laminin-binding integrins and a panel of laminins clearly demonstrate that the isoforms of both integrins and laminins differ in their binding specificities and affinities, and provide a molecular basis for better understanding of the adhesive interactions of cells with basement membranes of defined laminin compositions.

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Year:  2006        PMID: 16413178     DOI: 10.1016/j.matbio.2005.12.001

Source DB:  PubMed          Journal:  Matrix Biol        ISSN: 0945-053X            Impact factor:   11.583


  145 in total

Review 1.  Basic Biology of Extracellular Matrix in the Cardiovascular System, Part 1/4: JACC Focus Seminar.

Authors:  Gonzalo Del Monte-Nieto; Jens W Fischer; Daniel J Gorski; Richard P Harvey; Jason C Kovacic
Journal:  J Am Coll Cardiol       Date:  2020-05-05       Impact factor: 24.094

Review 2.  Laminin isoforms in development and disease.

Authors:  Susanne Schéele; Alexander Nyström; Madeleine Durbeej; Jan F Talts; Marja Ekblom; Peter Ekblom
Journal:  J Mol Med (Berl)       Date:  2007-04-11       Impact factor: 4.599

3.  Molecular basis of the recognition of nephronectin by integrin alpha8beta1.

Authors:  Yuya Sato; Toshihiko Uemura; Keisuke Morimitsu; Ryoko Sato-Nishiuchi; Ri-Ichiroh Manabe; Junichi Takagi; Masashi Yamada; Kiyotoshi Sekiguchi
Journal:  J Biol Chem       Date:  2009-04-02       Impact factor: 5.157

4.  The C-terminal region of laminin beta chains modulates the integrin binding affinities of laminins.

Authors:  Yukimasa Taniguchi; Hiroyuki Ido; Noriko Sanzen; Maria Hayashi; Ryoko Sato-Nishiuchi; Sugiko Futaki; Kiyotoshi Sekiguchi
Journal:  J Biol Chem       Date:  2009-01-15       Impact factor: 5.157

Review 5.  Laminins in Epithelial Cell Polarization: Old Questions in Search of New Answers.

Authors:  Karl S Matlin; Satu-Marja Myllymäki; Aki Manninen
Journal:  Cold Spring Harb Perspect Biol       Date:  2017-10-03       Impact factor: 10.005

6.  Integrin α3β1 regulates tumor cell responses to stromal cells and can function to suppress prostate cancer metastatic colonization.

Authors:  Afshin Varzavand; Justin M Drake; Robert U Svensson; Mary E Herndon; Bo Zhou; Michael D Henry; Christopher S Stipp
Journal:  Clin Exp Metastasis       Date:  2012-12-06       Impact factor: 5.150

7.  Isthmin targets cell-surface GRP78 and triggers apoptosis via induction of mitochondrial dysfunction.

Authors:  M Chen; Y Zhang; V C Yu; Y-S Chong; T Yoshioka; R Ge
Journal:  Cell Death Differ       Date:  2014-01-24       Impact factor: 15.828

Review 8.  Basement Membranes in the Worm: A Dynamic Scaffolding that Instructs Cellular Behaviors and Shapes Tissues.

Authors:  Matthew R Clay; David R Sherwood
Journal:  Curr Top Membr       Date:  2015-09-12       Impact factor: 3.049

9.  Scaffold-forming and Adhesive Contributions of Synthetic Laminin-binding Proteins to Basement Membrane Assembly.

Authors:  Karen K McKee; Stephanie Capizzi; Peter D Yurchenco
Journal:  J Biol Chem       Date:  2009-02-02       Impact factor: 5.157

10.  Integrins as antimetastatic targets of RGD-independent snake venom components in liver metastasis [corrected].

Authors:  Felix Rosenow; Rainer Ossig; Dorit Thormeyer; Peter Gasmann; Kerstin Schlüter; Georg Brunner; Jörg Haier; Johannes A Eble
Journal:  Neoplasia       Date:  2008-02       Impact factor: 5.715

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