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Volumn 55, Issue 12, 2014, Pages 7934-7944

Human eye development is characterized by coordinated expression of fibrillin isoforms

Author keywords

Ciliary zonule; Extracellular matrix; Fibrillin; Marfan syndrome; Ocular development

Indexed keywords

FIBRILLIN; FIBRILLIN 1; FIBRILLIN 2; FIBRILLIN 3; GLYCOPROTEIN; ISOPROTEIN; UNCLASSIFIED DRUG; ACTIN BINDING PROTEIN; CONTRACTILE PROTEIN; MICROFIBRILLAR PROTEIN; SCLEROPROTEIN;

EID: 84916919995     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.14-15453     Document Type: Article
Times cited : (34)

References (42)
  • 1
    • 85194398137 scopus 로고    scopus 로고
    • Microfibrils and fibrillin
    • Mecham RP, ed. Berlin, Germany: Springer-Verlag
    • Hubmacher D, Reinhardt D. Microfibrils and fibrillin. In: Mecham RP, ed. The Extracellular Matrix: An Overview. Berlin, Germany: Springer-Verlag; 2011: 233-265.
    • (2011) The Extracellular Matrix: An Overview , pp. 233-265
    • Hubmacher, D.1    Reinhardt, D.2
  • 2
    • 0028854569 scopus 로고
    • Immunohistochemical localization of fibrillin in human ocular tissues. Relevance to the Marfan syndrome
    • Wheatley HM, Traboulsi EI, Flowers BE, et al. Immunohistochemical localization of fibrillin in human ocular tissues. Relevance to the Marfan syndrome. Arch Ophthalmol. 1995; 113: 103-109.
    • (1995) Arch Ophthalmol , vol.113 , pp. 103-109
    • Wheatley, H.M.1    Traboulsi, E.I.2    Flowers, B.E.3
  • 3
    • 0026029066 scopus 로고
    • Extraction of extendable beaded structures and their identification as fibrillin-containing extracellular matrix microfibrils
    • Keene DR, Maddox BK, Kuo HJ, Sakai LY, Glanville RW. Extraction of extendable beaded structures and their identification as fibrillin-containing extracellular matrix microfibrils. J Histochem Cytochem. 1991; 39: 441-449.
    • (1991) J Histochem Cytochem , vol.39 , pp. 441-449
    • Keene, D.R.1    Maddox, B.K.2    Kuo, H.J.3    Sakai, L.Y.4    Glanville, R.W.5
  • 4
    • 43249105339 scopus 로고    scopus 로고
    • Ocular features of Marfan syndrome: Diagnosis and management
    • Nahum Y, Spierer A. Ocular features of Marfan syndrome: diagnosis and management. Isr Med Assoc J. 2008; 10: 179-181.
    • (2008) Isr Med Assoc J , vol.10 , pp. 179-181
    • Nahum, Y.1    Spierer, A.2
  • 5
    • 26944481486 scopus 로고    scopus 로고
    • Autosomal dominant Weill-Marchesani syndrome and glaucoma management
    • Saricaoglu MS, Sengun A, Karakurt A, Colluoglu Z. Autosomal dominant Weill-Marchesani syndrome and glaucoma management. Saudi Med J. 2005; 26: 1468-1469.
    • (2005) Saudi Med J , vol.26 , pp. 1468-1469
    • Saricaoglu, M.S.1    Sengun, A.2    Karakurt, A.3    Colluoglu, Z.4
  • 6
    • 4644236402 scopus 로고    scopus 로고
    • Surgical treatment of advanced chronic angle closure glaucoma in Weill-Marchesani syndrome
    • Harasymowycz P, Wilson R. Surgical treatment of advanced chronic angle closure glaucoma in Weill-Marchesani syndrome. J Pediatr Ophthalmol Strabismus. 2004; 41: 295-299.
    • (2004) J Pediatr Ophthalmol Strabismus , vol.41 , pp. 295-299
    • Harasymowycz, P.1    Wilson, R.2
  • 7
    • 0037238770 scopus 로고    scopus 로고
    • In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome
    • Faivre L, Gorlin RJ, Wirtz MK, et al. In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome. J Med Genet. 2003; 40: 34-36.
    • (2003) J Med Genet , vol.40 , pp. 34-36
    • Faivre, L.1    Gorlin, R.J.2    Wirtz, M.K.3
  • 10
    • 84911391197 scopus 로고    scopus 로고
    • Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration
    • Ratnapriya R, Zhan X, Fariss RN, et al. Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. Hum Mol Genet. 2014; 23: 5827-5837.
    • (2014) Hum Mol Genet , vol.23 , pp. 5827-5837
    • Ratnapriya, R.1    Zhan, X.2    Fariss, R.N.3
  • 11
    • 0033868391 scopus 로고    scopus 로고
    • Microfibril abnormalities of the lens capsule in patients with Marfan syndrome and ectopia lentis
    • Traboulsi EI, Whittum-Hudson JA, Mir SH, Maumenee IH. Microfibril abnormalities of the lens capsule in patients with Marfan syndrome and ectopia lentis. Ophthalmic Genet. 2000; 21: 9-15.
    • (2000) Ophthalmic Genet , vol.21 , pp. 9-15
    • Traboulsi, E.I.1    Whittum-Hudson, J.A.2    Mir, S.H.3    Maumenee, I.H.4
  • 12
    • 0031975962 scopus 로고    scopus 로고
    • A comparative histologic study of the fibrillin microfibrillar system in the lens capsule of normal subjects and subjects with Marfan syndrome
    • Mir S, Wheatley HM, Hussels IE, Whittum-Hudson JA, Traboulsi EI. A comparative histologic study of the fibrillin microfibrillar system in the lens capsule of normal subjects and subjects with Marfan syndrome. Invest Ophthalmol Vis Sci. 1998; 39: 84-93.
    • (1998) Invest Ophthalmol Vis Sci , vol.39 , pp. 84-93
    • Mir, S.1    Wheatley, H.M.2    Hussels, I.E.3    Whittum-Hudson, J.A.4    Traboulsi, E.I.5
  • 13
    • 84893478585 scopus 로고    scopus 로고
    • Nonselective assembly of fibrillin 1 and fibrillin 2 in the rodent ocular zonule and in cultured cells: Implications for Marfan syndrome
    • Beene LC, Wang LW, Hubmacher D, et al. Nonselective assembly of fibrillin 1 and fibrillin 2 in the rodent ocular zonule and in cultured cells: implications for Marfan syndrome. Invest Ophthalmol Vis Sci. 2013; 54: 8337-8344.
    • (2013) Invest Ophthalmol Vis Sci , vol.54 , pp. 8337-8344
    • Beene, L.C.1    Wang, L.W.2    Hubmacher, D.3
  • 14
    • 0037184979 scopus 로고    scopus 로고
    • Homo-and heterotypic fibrillin-1 and-2 interactions constitute the basis for the assembly of microfibrils
    • Lin G, Tiedemann K, Vollbrandt T, et al. Homo-and heterotypic fibrillin-1 and-2 interactions constitute the basis for the assembly of microfibrils. J Biol Chem. 2002; 277: 50795-50804.
    • (2002) J Biol Chem , vol.277 , pp. 50795-50804
    • Lin, G.1    Tiedemann, K.2    Vollbrandt, T.3
  • 15
    • 0037462816 scopus 로고    scopus 로고
    • Fibrillins can coassemble in fibrils, but fibrillin fibril composition displays cellspecific differences
    • Charbonneau NL, Dzamba BJ, Ono RN, et al. Fibrillins can coassemble in fibrils, but fibrillin fibril composition displays cellspecific differences. J Biol Chem. 2003; 278: 2740-2749.
    • (2003) J Biol Chem , vol.278 , pp. 2740-2749
    • Charbonneau, N.L.1    Dzamba, B.J.2    Ono, R.N.3
  • 16
    • 0029023792 scopus 로고
    • Developmental expression of fibrillin genes suggests heterogeneity of extracellular microfibrils
    • Zhang H, Hu W, Ramirez F. Developmental expression of fibrillin genes suggests heterogeneity of extracellular microfibrils. J Cell Biol. 1995; 129: 1165-1176.
    • (1995) J Cell Biol , vol.129 , pp. 1165-1176
    • Zhang, H.1    Hu, W.2    Ramirez, F.3
  • 17
    • 0029159521 scopus 로고
    • Fibrillin-1 and fibrillin-2 show temporal and tissue-specific regulation of expression in developing elastic tissues
    • Mariencheck MC, Davis EC, Zhang H, et al. Fibrillin-1 and fibrillin-2 show temporal and tissue-specific regulation of expression in developing elastic tissues. Connect Tissue Res. 1995; 31: 87-97.
    • (1995) Connect Tissue Res , vol.31 , pp. 87-97
    • Mariencheck, M.C.1    Davis, E.C.2    Zhang, H.3
  • 21
    • 84875935243 scopus 로고    scopus 로고
    • Development, composition, and structural arrangements of the ciliary zonule of the mouse
    • Shi Y, Tu Y, De Maria A, Mecham RP, Bassnett S. Development, composition, and structural arrangements of the ciliary zonule of the mouse. Invest Ophthalmol Vis Sci. 2013; 54: 2504-2515.
    • (2013) Invest Ophthalmol Vis Sci , vol.54 , pp. 2504-2515
    • Shi, Y.1    Tu, Y.2    De Maria, A.3    Mecham, R.P.4    Bassnett, S.5
  • 22
    • 84911448979 scopus 로고    scopus 로고
    • Latent TGFbeta binding protein-2 is essential for the development of ciliary zonule microfibrils
    • Inoue T, Ohbayashi T, Fujikawa Y, et al. Latent TGFbeta binding protein-2 is essential for the development of ciliary zonule microfibrils. Hum Mol Genet. 2014; 23: 5672-5682.
    • (2014) Hum Mol Genet , vol.23 , pp. 5672-5682
    • Inoue, T.1    Ohbayashi, T.2    Fujikawa, Y.3
  • 23
    • 71849096809 scopus 로고    scopus 로고
    • Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature
    • Morales J, Al-Sharif L, Khalil DS, et al. Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature. Am J Hum Genet. 2009; 85: 558-568.
    • (2009) Am J Hum Genet , vol.85 , pp. 558-568
    • Morales, J.1    Al-Sharif, L.2    Khalil, D.S.3
  • 24
    • 6344237724 scopus 로고    scopus 로고
    • ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndrome
    • Dagoneau N, Benoist-Lasselin C, Huber C, et al. ADAMTS10 mutations in autosomal recessive Weill-Marchesani syndrome. Am J Hum Genet. 2004; 75: 801-806.
    • (2004) Am J Hum Genet , vol.75 , pp. 801-806
    • Dagoneau, N.1    Benoist-Lasselin, C.2    Huber, C.3
  • 25
    • 77953809725 scopus 로고    scopus 로고
    • LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma
    • Desir J, Sznajer Y, Depasse F, et al. LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma. Eur J Hum Genet. 2010; 18: 761-767.
    • (2010) Eur J Hum Genet , vol.18 , pp. 761-767
    • Desir, J.1    Sznajer, Y.2    Depasse, F.3
  • 26
    • 70349578331 scopus 로고    scopus 로고
    • Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma
    • Narooie-Nejad M, Paylakhi SH, Shojaee S, et al. Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma. Hum Mol Genet. 2009; 18: 3969-3977.
    • (2009) Hum Mol Genet , vol.18 , pp. 3969-3977
    • Narooie-Nejad, M.1    Paylakhi, S.H.2    Shojaee, S.3
  • 28
    • 62649175429 scopus 로고    scopus 로고
    • A homozygous mutation in ADAMTSL4 causes autosomal-recessive isolated ectopia lentis
    • Ahram D, Sato TS, Kohilan A, et al. A homozygous mutation in ADAMTSL4 causes autosomal-recessive isolated ectopia lentis. Am J Hum Genet. 2009; 84: 274-278.
    • (2009) Am J Hum Genet , vol.84 , pp. 274-278
    • Ahram, D.1    Sato, T.S.2    Kohilan, A.3
  • 29
    • 76649101776 scopus 로고    scopus 로고
    • Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral ectopia lentis
    • Greene VB, Stoetzel C, Pelletier V, et al. Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral ectopia lentis. Ophthalmic Genet. 2010; 31: 47-51.
    • (2010) Ophthalmic Genet , vol.31 , pp. 47-51
    • Greene, V.B.1    Stoetzel, C.2    Pelletier, V.3
  • 30
    • 54449085747 scopus 로고    scopus 로고
    • Deficiency in microfibril-associated glycoprotein-1 leads to complex phenotypes in multiple organ systems
    • Weinbaum JS, Broekelmann TJ, Pierce RA, et al. Deficiency in microfibril-associated glycoprotein-1 leads to complex phenotypes in multiple organ systems. J Biol Chem. 2008; 283: 25533-25543.
    • (2008) J Biol Chem , vol.283 , pp. 25533-25543
    • Weinbaum, J.S.1    Broekelmann, T.J.2    Pierce, R.A.3
  • 31
    • 0035929624 scopus 로고    scopus 로고
    • Interactions of fibrillin-1 with heparin/heparan sulfate, implications for microfibrillar assembly
    • Tiedemann K, Batge B, Muller PK, Reinhardt DP. Interactions of fibrillin-1 with heparin/heparan sulfate, implications for microfibrillar assembly. J Biol Chem. 2001; 276: 36035-36042.
    • (2001) J Biol Chem , vol.276 , pp. 36035-36042
    • Tiedemann, K.1    Batge, B.2    Muller, P.K.3    Reinhardt, D.P.4
  • 32
    • 0036152086 scopus 로고    scopus 로고
    • Development of the mouse retinal vasculature: Angiogenesis versus vasculogenesis
    • Fruttiger M. Development of the mouse retinal vasculature: angiogenesis versus vasculogenesis. Invest Ophthalmol Vis Sci. 2002; 43: 522-527.
    • (2002) Invest Ophthalmol Vis Sci , vol.43 , pp. 522-527
    • Fruttiger, M.1
  • 33
    • 1242271343 scopus 로고    scopus 로고
    • Differential expression of fibrillin-3 adds to microfibril variety in human and avian, but not rodent, connective tissues
    • Corson GM, Charbonneau NL, Keene DR, Sakai LY. Differential expression of fibrillin-3 adds to microfibril variety in human and avian, but not rodent, connective tissues. Genomics. 2004; 83: 461-472.
    • (2004) Genomics , vol.83 , pp. 461-472
    • Corson, G.M.1    Charbonneau, N.L.2    Keene, D.R.3    Sakai, L.Y.4
  • 34
    • 80052927249 scopus 로고    scopus 로고
    • Genetic and functional linkage between ADAMTS superfamily proteins and fibrillin-1: A novel mechanism influencing microfibril assembly and function
    • Hubmacher D, Apte SS. Genetic and functional linkage between ADAMTS superfamily proteins and fibrillin-1: a novel mechanism influencing microfibril assembly and function. Cell Mol Life Sci. 2011; 68: 3137-3148.
    • (2011) Cell Mol Life Sci , vol.68 , pp. 3137-3148
    • Hubmacher, D.1    Apte, S.S.2
  • 35
    • 84858826597 scopus 로고    scopus 로고
    • ADAMTSL4, a secreted glycoprotein widely distributed in the eye, binds fibrillin-1 microfibrils and accelerates microfibril biogenesis
    • Gabriel LA, Wang LW, Bader H, et al. ADAMTSL4, a secreted glycoprotein widely distributed in the eye, binds fibrillin-1 microfibrils and accelerates microfibril biogenesis. Invest Ophthalmol Vis Sci. 2012; 53: 461-469.
    • (2012) Invest Ophthalmol Vis Sci , vol.53 , pp. 461-469
    • Gabriel, L.A.1    Wang, L.W.2    Bader, H.3
  • 36
    • 79955753992 scopus 로고    scopus 로고
    • ADAMTS10 protein interacts with fibrillin-1 and promotes its deposition in extracellular matrix of cultured fibroblasts
    • Kutz WE, Wang LW, Bader HL, et al. ADAMTS10 protein interacts with fibrillin-1 and promotes its deposition in extracellular matrix of cultured fibroblasts. J Biol Chem. 2011; 286: 17156-17167.
    • (2011) J Biol Chem , vol.286 , pp. 17156-17167
    • Kutz, W.E.1    Wang, L.W.2    Bader, H.L.3
  • 37
    • 34247501749 scopus 로고    scopus 로고
    • LTBP-2 specifically interacts with the amino-terminal region of fibrillin-1 and competes with LTBP-1 for binding to this microfibrillar protein
    • Hirani R, Hanssen E, Gibson MA. LTBP-2 specifically interacts with the amino-terminal region of fibrillin-1 and competes with LTBP-1 for binding to this microfibrillar protein. Matrix Biol. 2007; 26: 213-223.
    • (2007) Matrix Biol , vol.26 , pp. 213-223
    • Hirani, R.1    Hanssen, E.2    Gibson, M.A.3
  • 38
    • 74049160847 scopus 로고    scopus 로고
    • Functional consequences of homocysteinylation of the elastic fiber proteins fibrillin-1 and tropoelastin
    • Hubmacher D, Cirulis JT, Miao M, Keeley FW, Reinhardt DP. Functional consequences of homocysteinylation of the elastic fiber proteins fibrillin-1 and tropoelastin. J Biol Chem. 2010; 285: 1188-1198.
    • (2010) J Biol Chem , vol.285 , pp. 1188-1198
    • Hubmacher, D.1    Cirulis, J.T.2    Miao, M.3    Keeley, F.W.4    Reinhardt, D.P.5
  • 39
    • 27144498253 scopus 로고    scopus 로고
    • Modification of the structure and function of fibrillin-1 by homocysteine suggests a potential pathogenetic mechanism in homocystinuria
    • Hubmacher D, Tiedemann K, Bartels R, et al. Modification of the structure and function of fibrillin-1 by homocysteine suggests a potential pathogenetic mechanism in homocystinuria. J Biol Chem. 2005; 280: 34946-34955.
    • (2005) J Biol Chem , vol.280 , pp. 34946-34955
    • Hubmacher, D.1    Tiedemann, K.2    Bartels, R.3
  • 41
    • 84858394862 scopus 로고    scopus 로고
    • The evolution of extracellular fibrillins and their functional domains
    • Piha-Gossack A, Sossin W, Reinhardt DP. The evolution of extracellular fibrillins and their functional domains. PLoS One. 2012; 7: e33560.
    • (2012) PLoS One , vol.7
    • Piha-Gossack, A.1    Sossin, W.2    Reinhardt, D.P.3
  • 42
    • 38449103731 scopus 로고    scopus 로고
    • Compositional differences between infant and adult human corneal basement membranes
    • Kabosova A, Azar DT, Bannikov GA, et al. Compositional differences between infant and adult human corneal basement membranes. Invest Ophthalmol Vis Sci. 2007; 48: 4989-4999.
    • (2007) Invest Ophthalmol Vis Sci , vol.48 , pp. 4989-4999
    • Kabosova, A.1    Azar, D.T.2    Bannikov, G.A.3


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