Assembly of fibrillin microfibrils governs extracellular deposition of latent TGF beta

作者：Massam Wu Teresa; Chiu Maybo; Choudhury Rawshan; Chaudhry Shazia S; Baldwin Andrew K; McGovern Amanda; Baldock Clair; Shuttleworth C Adrian; Kielty Cay M^*

来源：Journal of Cell Science, 2010, 123(17): 3006-3018.

DOI：10.1242/jcs.073437

• Latent TGF beta-binding protein 1 (LTBP-1)
• Fibrillin-1
• Microfibrils
• MAGP-1
• Heparin
• Fibulin-4

Control of the bioavailability of the growth factor TGF beta is essential for tissue formation and homeostasis, yet precisely how latent TGF beta is incorporated into the extracellular matrix is unknown. Here, we show that deposition of a large latent TGF beta complex (LLC), which contains latent TGF beta-binding protein 1 (LTBP-1), is directly dependent on the pericellular assembly of fibrillin microfibrils, which interact with fibronectin during higher-order fibrillogenesis. LTBP-1 formed pericellular arrays that colocalized with microfibrils, whereas fibrillin knockdown inhibited fibrillar LTBP-1 and/or LLC deposition. Blocking alpha 5 beta 1 integrin or supplementing cultures with heparin, which both inhibited microfibril assembly, disrupted LTBP-1 deposition and enhanced Smad2 phosphorylation. Full-length LTBP-1 bound only weakly to N-terminal pro-fibrillin-1, but this association was strongly enhanced by heparin. The microfibril-associated glycoprotein MAGP-1 (MFAP-2) inhibited LTBP-1 binding to fibrillin-1 and stimulated Smad2 phosphorylation. By contrast, fibulin-4, which interacted strongly with full-length LTBP-1, did not induce Smad2 phosphorylation. Thus, LTBP-1 and/or LLC deposition is dependent on pericellular microfibril assembly and is governed by complex interactions between LTBP-1, heparan sulfate, fibrillin-1 and microfibril-associated molecules. In this way, microfibrils control TGF beta bioavailability.

• 出版日期2010-9-1