{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,13]],"date-time":"2026-05-13T16:21:26Z","timestamp":1778689286283,"version":"3.51.4"},"reference-count":62,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2022,11,1]],"date-time":"2022-11-01T00:00:00Z","timestamp":1667260800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2022,11,1]],"date-time":"2022-11-01T00:00:00Z","timestamp":1667260800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2023,10,14]],"date-time":"2023-10-14T00:00:00Z","timestamp":1697241600000},"content-version":"am","delay-in-days":347,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"},{"start":{"date-parts":[[2022,11,1]],"date-time":"2022-11-01T00:00:00Z","timestamp":1667260800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2022,11,1]],"date-time":"2022-11-01T00:00:00Z","timestamp":1667260800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2022,11,1]],"date-time":"2022-11-01T00:00:00Z","timestamp":1667260800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2022,11,1]],"date-time":"2022-11-01T00:00:00Z","timestamp":1667260800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2022,11,1]],"date-time":"2022-11-01T00:00:00Z","timestamp":1667260800000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"funder":[{"DOI":"10.13039\/100020309","name":"Vanderbilt Vision Research Center, Vanderbilt University","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100020309","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["CA68485"],"award-info":[{"award-number":["CA68485"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["DK20593"],"award-info":[{"award-number":["DK20593"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["DK58404"],"award-info":[{"award-number":["DK58404"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["DK59637"],"award-info":[{"award-number":["DK59637"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["S10 RR023901"],"award-info":[{"award-number":["S10 RR023901"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000053","name":"National Eye Institute","doi-asserted-by":"publisher","award":["EY027746"],"award-info":[{"award-number":["EY027746"]}],"id":[{"id":"10.13039\/100000053","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000053","name":"National Eye Institute","doi-asserted-by":"publisher","award":["P30EY008126"],"award-info":[{"award-number":["P30EY008126"]}],"id":[{"id":"10.13039\/100000053","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100001818","name":"Research to Prevent Blindness","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100001818","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Matrix Biology"],"published-print":{"date-parts":[[2022,11]]},"DOI":"10.1016\/j.matbio.2022.10.001","type":"journal-article","created":{"date-parts":[[2022,10,7]],"date-time":"2022-10-07T21:44:25Z","timestamp":1665179065000},"page":"83-99","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":1,"special_numbering":"C","title":["Optic neuropathy associated with TGF\u03b2 dysregulation in mice with a glaucoma-causative mutation of ADAMTS10"],"prefix":"10.1016","volume":"113","author":[{"given":"Hang-Jing","family":"Wu","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rachel W.","family":"Kuchtey","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John","family":"Kuchtey","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.matbio.2022.10.001_bib0001","doi-asserted-by":"crossref","first-page":"807","DOI":"10.1007\/s00401-016-1609-2","article-title":"Glaucoma: the retina and beyond","volume":"132","author":"Davis","year":"2016","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.matbio.2022.10.001_bib0002","doi-asserted-by":"crossref","first-page":"702","DOI":"10.1016\/j.preteyeres.2012.07.001","article-title":"Critical pathogenic events underlying progression of neurodegeneration in glaucoma","volume":"31","author":"Calkins","year":"2012","journal-title":"Prog. Retin. Eye Res."},{"key":"10.1016\/j.matbio.2022.10.001_bib0003","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pgen.1001306","article-title":"Mapping of the disease locus and identification of ADAMTS10 as a candidate gene in a canine model of primary open angle glaucoma","volume":"7","author":"Kuchtey","year":"2011","journal-title":"PLOS Genet."},{"key":"10.1016\/j.matbio.2022.10.001_bib0004","doi-asserted-by":"crossref","first-page":"31493","DOI":"10.1074\/jbc.R109.052340","article-title":"A disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif (ADAMTS) superfamily: functions and mechanisms*","volume":"284","author":"Apte","year":"2009","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2022.10.001_bib0005","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0111941","article-title":"A novel missense mutation in ADAMTS10 in norwegian elkhound primary glaucoma","volume":"9","author":"Ahonen","year":"2014","journal-title":"PLOS One"},{"key":"10.1016\/j.matbio.2022.10.001_bib0006","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0143546","article-title":"A novel genome-wide association study approach using genotyping by exome sequencing leads to the identification of a primary open angle glaucoma associated inversion disrupting ADAMTS17","volume":"10","author":"Forman","year":"2015","journal-title":"PLOS One"},{"key":"10.1016\/j.matbio.2022.10.001_bib0007","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0140436","article-title":"Two independent mutations in ADAMTS17 are associated with primary open angle glaucoma in the basset hound and basset fauve de bretagne breeds of dog","volume":"10","author":"Oliver","year":"2015","journal-title":"PLOS One"},{"key":"10.1016\/j.matbio.2022.10.001_bib0008","doi-asserted-by":"crossref","first-page":"98","DOI":"10.2460\/ajvr.79.1.98","article-title":"Evaluation of ADAMTS17 in Chinese Shar-Pei with primary open-angle glaucoma, primary lens luxation, or both","volume":"79","author":"Oliver","year":"2018","journal-title":"Am. J. Vet. Res."},{"key":"10.1016\/j.matbio.2022.10.001_bib0009","doi-asserted-by":"crossref","first-page":"4883","DOI":"10.1038\/ncomms5883","article-title":"Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process","volume":"5","author":"Springelkamp","year":"2014","journal-title":"Nat. Commun."},{"key":"10.1016\/j.matbio.2022.10.001_bib0010","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1002\/gepi.21886","article-title":"Meta-analysis of genome-wide association studies identifies novel loci associated with optic disc morphology","volume":"39","author":"Springelkamp","year":"2015","journal-title":"Genet. Epidemiol."},{"key":"10.1016\/j.matbio.2022.10.001_bib0011","first-page":"438","article-title":"New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics","volume":"26","author":"Springelkamp","year":"2017","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.matbio.2022.10.001_bib0012","doi-asserted-by":"crossref","first-page":"1864","DOI":"10.1038\/s41467-018-03646-6","article-title":"Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases","volume":"9","author":"Iglesias","year":"2018","journal-title":"Nat. Commun."},{"key":"10.1016\/j.matbio.2022.10.001_bib0013","doi-asserted-by":"crossref","first-page":"1485","DOI":"10.1002\/humu.23299","article-title":"Identification and functional analysis of an ADAMTSL1 variant associated with a complex phenotype including congenital glaucoma, craniofacial, and other systemic features in a three-generation human pedigree","volume":"38","author":"Hendee","year":"2017","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.matbio.2022.10.001_bib0014","doi-asserted-by":"crossref","first-page":"801","DOI":"10.1086\/425231","article-title":"ADAMTS10 mutations in autosomal recessive weill-marchesani syndrome","volume":"75","author":"Dagoneau","year":"2004","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.matbio.2022.10.001_bib0015","doi-asserted-by":"crossref","first-page":"558","DOI":"10.1016\/j.ajhg.2009.09.011","article-title":"Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature","volume":"85","author":"Morales","year":"2009","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.matbio.2022.10.001_bib0016","doi-asserted-by":"crossref","first-page":"1425","DOI":"10.1002\/humu.20797","article-title":"Functional analysis of an ADAMTS10 signal peptide mutation in Weill-Marchesani syndrome demonstrates a long-range effect on secretion of the full-length enzyme","volume":"29","author":"Kutz","year":"2008","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.matbio.2022.10.001_bib0017","doi-asserted-by":"crossref","first-page":"34","DOI":"10.1136\/jmg.40.1.34","article-title":"In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome","volume":"40","author":"Faivre","year":"2003","journal-title":"J. Med. Genet."},{"key":"10.1016\/j.matbio.2022.10.001_bib0018","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pgen.1002425","article-title":"Microenvironmental regulation by fibrillin-1","volume":"8","author":"Sengle","year":"2012","journal-title":"PLOS Genet"},{"key":"10.1016\/j.matbio.2022.10.001_bib0019","doi-asserted-by":"crossref","first-page":"204","DOI":"10.1002\/ajmg.a.20289","article-title":"Clinical homogeneity and genetic heterogeneity in Weill\u2013Marchesani syndrome","volume":"123A","author":"Faivre","year":"2003","journal-title":"Am. J. Med. Genet. A"},{"key":"10.1016\/j.matbio.2022.10.001_bib0020","doi-asserted-by":"crossref","first-page":"3137","DOI":"10.1007\/s00018-011-0780-9","article-title":"Genetic and functional linkage between ADAMTS superfamily proteins and fibrillin-1: a novel mechanism influencing microfibril assembly and function","volume":"68","author":"Hubmacher","year":"2011","journal-title":"Cell. Mol. Life Sci."},{"key":"10.1016\/j.matbio.2022.10.001_bib0021","doi-asserted-by":"crossref","first-page":"17156","DOI":"10.1074\/jbc.M111.231571","article-title":"ADAMTS10 protein interacts with fibrillin-1 and promotes its deposition in extracellular matrix of cultured fibroblasts","volume":"286","author":"Kutz","year":"2011","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2022.10.001_bib0022","doi-asserted-by":"crossref","DOI":"10.1093\/hmg\/ddy276","article-title":"ADAMTS10-mediated tissue disruption in Weill\u2013Marchesani syndrome","author":"Mularczyk","year":"2018","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.matbio.2022.10.001_bib0023","doi-asserted-by":"crossref","DOI":"10.1167\/iovs.62.10.26","article-title":"Altered ocular fibrillin microfibril composition in mice with a glaucoma-causing mutation of ADAMTS10","volume":"62","author":"Wu","year":"2021","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.matbio.2022.10.001_bib0024","article-title":"ADAMTS10 inactivation in mice leads to persistence of ocular microfibrils subsequent to reduced fibrillin-2 cleavage","author":"Wang","year":"2018","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2022.10.001_bib0025","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1038\/352337a0","article-title":"Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene","volume":"352","author":"Dietz","year":"1991","journal-title":"Nature"},{"key":"10.1016\/j.matbio.2022.10.001_bib0026","doi-asserted-by":"crossref","first-page":"1359","DOI":"10.1136\/bjo.86.12.1359","article-title":"Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitus","volume":"86","author":"Comeglio","year":"2002","journal-title":"Br. J. Ophthalmol."},{"key":"10.1016\/j.matbio.2022.10.001_bib0027","doi-asserted-by":"crossref","first-page":"279","DOI":"10.1016\/j.gene.2016.07.033","article-title":"FBN1: the disease-causing gene for marfan syndrome and other genetic disorders","volume":"591","author":"Sakai","year":"2016","journal-title":"Gene"},{"key":"10.1016\/j.matbio.2022.10.001_bib0028","doi-asserted-by":"crossref","first-page":"616","DOI":"10.1016\/j.ceb.2009.05.005","article-title":"Extracellular microfibrils: contextual platforms for TGF\u03b2 and BMP signaling","volume":"21","author":"Ramirez","year":"2009","journal-title":"Curr. Opin. Cell Biol."},{"key":"10.1016\/j.matbio.2022.10.001_bib0029","doi-asserted-by":"crossref","first-page":"487","DOI":"10.3390\/biom10030487","volume":"10","author":"Tzavlaki","year":"2020","journal-title":"Biomolecules"},{"key":"10.1016\/j.matbio.2022.10.001_bib0030","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1038\/ng1116","article-title":"Dysregulation of TGF-\u03b2 activation contributes to pathogenesis in marfan syndrome","volume":"33","author":"Neptune","year":"2003","journal-title":"Nat. Genet."},{"key":"10.1016\/j.matbio.2022.10.001_bib0031","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1126\/science.1124287","article-title":"Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of marfan syndrome","volume":"312","author":"Habashi","year":"2006","journal-title":"Science"},{"key":"10.1016\/j.matbio.2022.10.001_bib0032","doi-asserted-by":"crossref","first-page":"4795","DOI":"10.1007\/s00018-019-03188-0","article-title":"Adamts17 is involved in skeletogenesis through modulation of BMP-Smad1\/5\/8 pathway","volume":"76","author":"Oichi","year":"2019","journal-title":"Cell. Mol. Life Sci."},{"key":"10.1016\/j.matbio.2022.10.001_bib0033","doi-asserted-by":"crossref","first-page":"279","DOI":"10.1007\/s00441-011-1274-7","article-title":"The role of TGF-\u03b2 in the pathogenesis of primary open-angle glaucoma","volume":"347","author":"Fuchshofer","year":"2012","journal-title":"Cell Tissue Res."},{"key":"10.1016\/j.matbio.2022.10.001_bib0034","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1016\/j.matbio.2015.05.003","article-title":"The microfibril-associated glycoproteins (MAGPs) and the microfibrillar niche","volume":"47","author":"Mecham","year":"2015","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2022.10.001_bib0035","doi-asserted-by":"crossref","first-page":"899","DOI":"10.1113\/jphysiol.2002.019703","article-title":"The scotopic threshold response of the dark-adapted electroretinogram of the mouse","volume":"543","author":"Saszik","year":"2002","journal-title":"J. Physiol."},{"key":"10.1016\/j.matbio.2022.10.001_bib0036","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1113\/jphysiol.2003.052738","article-title":"Ganglion cell contributions to the rat full-field electroretinogram","volume":"555","author":"Bui","year":"2004","journal-title":"J. Physiol."},{"key":"10.1016\/j.matbio.2022.10.001_bib0037","doi-asserted-by":"crossref","first-page":"2176","DOI":"10.1016\/j.visres.2010.08.014","article-title":"ERG changes in albino and pigmented mice after optic nerve transection","volume":"50","author":"Alarc\u00f3n-Mart\u00ednez","year":"2010","journal-title":"Vis. Res."},{"key":"10.1016\/j.matbio.2022.10.001_bib0038","doi-asserted-by":"crossref","first-page":"3766","DOI":"10.1167\/iovs.14-13895","article-title":"Monitoring retinal morphologic and functional changes in mice following optic nerve crush","volume":"55","author":"Liu","year":"2014","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.matbio.2022.10.001_bib0039","doi-asserted-by":"crossref","DOI":"10.1523\/ENEURO.0260-18.2018","article-title":"Enlarged optic nerve axons and reduced visual function in mice with defective microfibrils","volume":"5","author":"Wu","year":"2018","journal-title":"eNeuro"},{"key":"10.1016\/j.matbio.2022.10.001_bib0040","doi-asserted-by":"crossref","first-page":"3984","DOI":"10.1167\/iovs.18-23885","article-title":"Ultrastructural morphology of the optic nerve head in aged and glaucomatous mice","volume":"59","author":"Zhu","year":"2018","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.matbio.2022.10.001_bib0041","doi-asserted-by":"crossref","DOI":"10.1016\/j.exer.2015.11.016","article-title":"Early astrocyte redistribution in the optic nerve precedes axonopathy in the DBA\/2J mouse model of glaucoma","author":"Cooper","year":"2016","journal-title":"Exp. Eye Res."},{"key":"10.1016\/j.matbio.2022.10.001_bib0042","series-title":"Retinal Degenerative Diseases","first-page":"9","article-title":"Programmed cell death during retinal development of the mouse eye","author":"Braunger","year":"2014"},{"key":"10.1016\/j.matbio.2022.10.001_bib0043","doi-asserted-by":"crossref","first-page":"2173","DOI":"10.1002\/hep.24598","article-title":"Protease profiling of liver fibrosis reveals the ADAM metallopeptidase with thrombospondin type 1 motif, 1 as a central activator of transforming growth factor beta","volume":"54","author":"Bourd-Boittin","year":"2011","journal-title":"Hepatology"},{"key":"10.1016\/j.matbio.2022.10.001_bib0044","doi-asserted-by":"crossref","first-page":"956","DOI":"10.1093\/cvr\/cvz187","article-title":"ADAMTS16 activates latent TGF-\u03b2, accentuating fibrosis and dysfunction of the pressure-overloaded heart","volume":"116","author":"Yao","year":"2020","journal-title":"Cardiovasc. Res."},{"key":"10.1016\/j.matbio.2022.10.001_bib0045","doi-asserted-by":"crossref","first-page":"51208","DOI":"10.1074\/jbc.M409036200","article-title":"Discovery and characterization of a novel, widely expressed metalloprotease, ADAMTS10, and its proteolytic activation","volume":"279","author":"Somerville","year":"2004","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2022.10.001_bib0046","article-title":"A novel ADAMTS17 variant that causes Weill-Marchesani syndrome 4 alters fibrillin-1 and collagen type I deposition in the extracellular matrix","author":"Karoulias","year":"2019","journal-title":"Matrix Biol."},{"key":"10.1016\/j.matbio.2022.10.001_bib0047","doi-asserted-by":"crossref","DOI":"10.1017\/erm.2013.9","article-title":"Elastic fibres in health and disease","volume":"15","author":"Baldwin","year":"2013","journal-title":"Expert Rev. Mol. Med."},{"key":"10.1016\/j.matbio.2022.10.001_bib0048","doi-asserted-by":"crossref","DOI":"10.1167\/iovs.61.10.28","article-title":"Increased susceptibility to glaucomatous damage in microfibril deficient mice","volume":"61","author":"Wu","year":"2020","journal-title":"Invest. Ophthalmol. Vis. Sci."},{"key":"10.1016\/j.matbio.2022.10.001_bib0049","doi-asserted-by":"crossref","DOI":"10.1242\/dmm.037283","article-title":"Targeted deletion of fibrillin-1 in the mouse eye results in ectopia lentis and other ocular phenotypes associated with Marfan syndrome","volume":"12","author":"Jones","year":"2019","journal-title":"Dis. Model. Mech."},{"key":"10.1016\/j.matbio.2022.10.001_bib0050","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0183370","article-title":"Biometric and structural ocular manifestations of marfan syndrome","volume":"12","author":"Gehle","year":"2017","journal-title":"PLOS One"},{"key":"10.1016\/j.matbio.2022.10.001_bib0051","doi-asserted-by":"crossref","first-page":"1026","DOI":"10.1016\/j.jcrs.2009.01.029","article-title":"Biometric and corneal topographic characteristics in patients with Weill-Marchesani syndrome","volume":"35","author":"Razeghinejad","year":"2009","journal-title":"J. Cataract Refract. Surg."},{"key":"10.1016\/j.matbio.2022.10.001_bib0052","doi-asserted-by":"crossref","first-page":"14246","DOI":"10.1523\/JNEUROSCI.0991-13.2013","article-title":"TGF-\u03b2 signaling protects retinal neurons from programmed cell death during the development of the mammalian eye","volume":"33","author":"Braunger","year":"2013","journal-title":"J. Neurosci."},{"key":"10.1016\/j.matbio.2022.10.001_bib0053","doi-asserted-by":"crossref","DOI":"10.3389\/fmolb.2022.989851","article-title":"ADAMTS10 controls transforming growth factor \u03b2 family signaling that contributes to retinal ganglion cell development","volume":"9","author":"Wareham","year":"2022","journal-title":"Front. Mol. Biosci."},{"key":"10.1016\/j.matbio.2022.10.001_bib0054","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1093\/jb\/mvs089","article-title":"Matrix control of transforming growth factor-\u03b2 function","volume":"152","author":"Horiguchi","year":"2012","journal-title":"J. Biochem."},{"key":"10.1016\/j.matbio.2022.10.001_bib0055","doi-asserted-by":"crossref","first-page":"163","DOI":"10.1101\/gad.14.2.163","article-title":"Cell surface-localized matrix metalloproteinase-9 proteolytically activates TGF-\u03b2 and promotes tumor invasion and angiogenesis","volume":"14","author":"Yu","year":"2000","journal-title":"Genes Dev."},{"key":"10.1016\/j.matbio.2022.10.001_bib0056","doi-asserted-by":"crossref","first-page":"309","DOI":"10.1083\/jcb.109.1.309","article-title":"Inhibition of endothelial cell movement by pericytes and smooth muscle cells: activation of a latent transforming growth factor-beta 1-like molecule by plasmin during co-culture","volume":"109","author":"Sato","year":"1989","journal-title":"J. Cell Biol."},{"key":"10.1016\/j.matbio.2022.10.001_bib0057","doi-asserted-by":"crossref","first-page":"923","DOI":"10.1083\/jcb.122.4.923","article-title":"Thrombospondin causes activation of latent transforming growth factor-beta secreted by endothelial cells by a novel mechanism","volume":"122","author":"Schultz-Cherry","year":"1993","journal-title":"J. Cell Biol."},{"key":"10.1016\/j.matbio.2022.10.001_bib0058","doi-asserted-by":"crossref","first-page":"7304","DOI":"10.1074\/jbc.270.13.7304","article-title":"Regulation of transforming growth factor-\u03b2 activation by discrete sequences of thrombospondin 1 (\u2217)","volume":"270","author":"Schultz-Cherry","year":"1995","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2022.10.001_bib0059","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1016\/S1359-6101(99)00029-5","article-title":"Activation of latent TGF-\u03b2 by thrombospondin-1: mechanisms and physiology","volume":"11","author":"Murphy-Ullrich","year":"2000","journal-title":"Cytokine Growth Factor Rev."},{"key":"10.1016\/j.matbio.2022.10.001_bib0060","doi-asserted-by":"crossref","first-page":"2740","DOI":"10.1074\/jbc.M209201200","article-title":"Fibrillins can co-assemble in fibrils, but fibrillin fibril composition displays cell-specific differences*","volume":"278","author":"Charbonneau","year":"2003","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.matbio.2022.10.001_bib0061","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0201719","article-title":"Differential effects of angiotensin II type I receptor blockers on reducing intraocular pressure and TGF\u03b2 signaling in the mouse retina","volume":"13","author":"Hazlewood","year":"2018","journal-title":"PLOS One"},{"key":"10.1016\/j.matbio.2022.10.001_bib0062","doi-asserted-by":"crossref","first-page":"e58","DOI":"10.1002\/cpim.58","article-title":"Proximity ligation assay (PLA)","volume":"123","author":"Alam","year":"2018","journal-title":"Curr. Protoc. Immunol."}],"container-title":["Matrix Biology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0945053X22001238?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0945053X22001238?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,15]],"date-time":"2025-10-15T19:03:30Z","timestamp":1760555010000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0945053X22001238"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,11]]},"references-count":62,"alternative-id":["S0945053X22001238"],"URL":"https:\/\/doi.org\/10.1016\/j.matbio.2022.10.001","relation":{},"ISSN":["0945-053X"],"issn-type":[{"value":"0945-053X","type":"print"}],"subject":[],"published":{"date-parts":[[2022,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Optic neuropathy associated with TGF\u03b2 dysregulation in mice with a glaucoma-causative mutation of ADAMTS10","name":"articletitle","label":"Article Title"},{"value":"Matrix Biology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.matbio.2022.10.001","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2023 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}