Physiological and pathological implications of laminins: From the gene to the protein

References

• Jones JCR, Dehart GW, Gonzales M, Goldfinger LE. Laminins: An overview. Microsc Res Tech 2000; 51: 211–213
   PubMedGoogle Scholar
• Timpl R, Rohde H, Robey PG, Rennard SI, Foidart JM, Martin GR. Laminin: A glycoprotein from basement membranes. J Biol Chem 1979; 254: 9933–9937
   PubMed Web of Science ®Google Scholar
• Sasaki T, Fässler R, Hohenester E. Laminin: The crux of basement membrane assembly. J Cell Biol 2004; 164: 959–963
   PubMed Web of Science ®Google Scholar
• Quondamatteo F. Assembly, stability and integrity of basement membranes in vivo. Histochem J 2002; 34: 369–381
   PubMedGoogle Scholar
• Burgeson RE, Chiquet M, Deutzmann R, Ekblom P, Engel J, Kleinman H. A nomenclature for the laminins. Matrix Biol 1994; 14: 209–211
   PubMed Web of Science ®Google Scholar
• Timpl R, Tisi D, Talts JF, Andac A, Sasaki E, Hohenester E. Structure and function of laminin LG modules. Matrix Biol 2000; 19: 309–317
   PubMed Web of Science ®Google Scholar
• Aumailley M, Bruckner-Tuderman L, Carter WG, Deutzmann R, Edgar D, Ekblom P, Engel J, Engvall E, Hohenester E, Jones JC, Kleinman HK, Marinkovich MP, Martin GR, Mayer U, Meneguzzi G, Miner JH, Miyazaki K, Patarroyo M, Paulsson M, Quaranta V, Sanes JR, Sasaki T, Sekiguchi K, Sorokin LM, Talts JF, Tryggvason K, Uitto J, Virtanen I, von der Mark K, Wewer UM, Yamada Y, Yurchenco PD. A simplified laminin nomenclature. Matrix Biol 2005; 24: 326–332
   PubMed Web of Science ®Google Scholar
• Tunggal P, Smyth N, Paulsson M, OTT MC. Laminins: Structure and genetic regulation. Microsc Res Tech 2000; 51: 214–227
   PubMedGoogle Scholar
• Denzer AJ, Schulthess T, Fauser C, Schumacher B, Kammerer RA, Engel J. Electron microscopic structure of agrin and mapping of its binding site in laminin-1. ELBO 1998; 17: 335–343
   PubMedGoogle Scholar
• Appella E, Weber IT, Blasi F. Structure and function of epidermal growth factor-like regions in proteins. FEBS Lett 1988; 231: 1–4
   PubMed Web of Science ®Google Scholar
• Online Mendelian inheritance in man—OMIN [Internet]. Baltimore, USA: Johns Hopkins University. 2005 June–December—[cited 2006 March]; available from: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db = OMIM.
   Google Scholar
• Belkin AM, Stepp MA. Integrins as receptors for laminins. Microsc Res Tech 2000; 51: 280–301
   PubMed Web of Science ®Google Scholar
• Hynes RO. Cell adhesion: Old and new questions. Trends Cell Biol 1999; 9: M33–M37
   PubMed Web of Science ®Google Scholar
• Eble JA, Wucherpfennig KW, Gauthier L, Dersch P, Krukonis E, Isberg RR, Hemler ME. Recombinant soluble human α3β1 integrin: Purification, processing, regulation, and specific binding to laminin-5 and invasin in a mutually exclusive manner. Biochemistry 1998; 37: 10945–10955
   PubMed Web of Science ®Google Scholar
• Yao CC, Ziober BL, Squillace RM, Kramer RH. α7 Integrin mediates cell adhesion and migration on specific laminin isoforms. J Biol Chem 1996; 271: 25598–25603
   PubMed Web of Science ®Google Scholar
• Yao CC, Ziober BL, Sutherland AE, Mendrick DL, Kramer RH. Laminins promote the locomotion of skeletal myoblasts via the α7 integrin receptor. J Cell Sci 1996; 109: 3139–3150
   PubMedGoogle Scholar
• Mercurio AM. Laminin receptors: Achieving specificity through cooperation. Trends Cell Biol 1995; 5: 419–423
   PubMed Web of Science ®Google Scholar
• Mecham RP. Laminin receptors. Annu Rev Cell Biol 1991; 7: 71–91
   PubMedGoogle Scholar
• Klafky E, Williams R, Yoo CC, Ziober B, Kramer R, Sutherland A. Trophoblast-specific expression and function of the integrin alpha 7 subunit in the peri-implatation mouse embryo. Dev Biol 2001; 239: 161–175
   PubMedGoogle Scholar
• Ekblom P, Lonai P, Talts JF. Expression and biological role of laminin-1. Matrix Biol 2003; 22: 35–47
   PubMed Web of Science ®Google Scholar
• Murray P, Edgar D. Regulation of programmed cell death by basement membranes in embryonic development. J Cell Biol 2000; 150: 1215–1221
   PubMedGoogle Scholar
• Smyth N, Vatansever HS, Murray P, Meyer M, Frie C, Paulsson M, Edgar D. Absence of basement membranes after targeting the LAMC1 gene results in embryonic lethality due to failure of endoderm differentiation. J Cell Biol 1999; 144: 151–160
   PubMed Web of Science ®Google Scholar
• Makrigiannakis A, Zoumakis E, Kalantaridou S, Chrousos G. Endometrial and placental CRH as regulators of human embryo implantation. J Reprod Immunol 2004; 62: 53–59
   PubMedGoogle Scholar
• Miner JH, Li C, MuddJ L, Go G, Sutherland AE. Compositional and structural requirements for laminin and basement membranes during mouse embryo implantation and gastrulation. Development 2004; 131: 2247–2256
   PubMed Web of Science ®Google Scholar
• Qureshi F, Yang Y, Jaques SM, Johnson MP, Naparstek J, Ulmansky R, Schuger L. Anti-DNA antibodies cross-reacting with laminin inhibit trophoblast attachment and migration: Implications for recurrent pregnancy loss in SLE patients. Am J Reprod Immunol 2000; 44: 136–142
   PubMedGoogle Scholar
• Inagaki J, Matsuura E, Nomizu M, Sugiura-Ogasawara M, Katano K, Kaihara K, Kobayashi K, Yasuda T, Aoki K. IgG anti-laminin-1 autoantibody and recurrent miscarriages. Am J Reprod Immunol 2001; 45: 232–238
   PubMed Web of Science ®Google Scholar
• Inagaki J, Sugiura-Ogasawara M, Nomizu M, Nakatsuka M, Ikuta K, Suzuki N, Ikuta K, Suzuki N, Kaihara K, Kobayashi K, Yasuda T, Shoenfeld Y, Aoki K, Matsuura E. An association of IgG antilaminin-1 autoantibodies with endometriosis in infertile patients. Hum Reprod 2003; 18: 544–549
   PubMedGoogle Scholar
• Miner JH. Renal basement membrana components. Kidney Int 1999; 56: 2016–2024
   PubMed Web of Science ®Google Scholar
• Klein G, Langegger M, Timpl R, Ekblom P. Role of laminin α chain in the development of epithelial cell polarity. Cell 1988; 55: 331–341
   PubMed Web of Science ®Google Scholar
• Patton BL. Laminins of the neuromuscular system. Microsc Res Tech 2000; 51: 247–261
   PubMedGoogle Scholar
• Patton BL, Connolly AM, Martin PT, Cunningham JM, Shobhna M, Pestronk A. Distribution of ten laminin chains in dystrophic and regenerating muscles. Neuromusc Disord 1999; 9: 423–433
   PubMed Web of Science ®Google Scholar
• Miyagoe-Suzuki Y, Nakagawa M, Takeda S. Merosin and congenital muscular dystrophy. Microsc Res Tech 2000; 48: 181–191
   PubMedGoogle Scholar
• Miner JH, Yurchenco PD. Laminin functions in tissue morphogenesis. Annu Rev Cell Dev Biol 2004; 20: 255–284
   PubMed Web of Science ®Google Scholar
• Tardy M. Role of laminin bioavailability in the astroglial permissivity for neuritic outgrowth. An Acad Bras Cienc 2002; 74: 683–690
   PubMedGoogle Scholar
• Miner JH, Cunningham J, Sanes JR. Roles for laminin in embryogenesis: Exencephaly, syndactyly, and placentopathy in mice lacking the laminin α5 chain. J Cell Biol 1998; 143: 1713–1723
   PubMed Web of Science ®Google Scholar
• Halfter W, Dong S, Yip YP, Willem M, Mayer U. A critical function of the pial basement membrane in cortical histogenesis. J Neurosci 2002; 22: 6029–6040
   PubMedGoogle Scholar
• Colognato H, Yurchenco PD. Form and function: The laminin family of heterotrimers. Dev Dyn 2000; 218: 213–234
   PubMed Web of Science ®Google Scholar
• Jones JC, Hopkinson SB, Goldfinger LE. Structure and assembly of hemidesmosomes. Bioessays 1998; 20: 488–494
   PubMed Web of Science ®Google Scholar
• Pulkkinen L, Uitto J. Mutation analysis and molecular genetics of epidermolysis bullosa. Matrix Biol 1999; 18: 29–42
   PubMed Web of Science ®Google Scholar
• Floeth M, Bruckner-Tuderman L. Digenic junctional epidermolysis bullosa: Mutations in COL17A1 and LAMB3 gnees. Am J Hum Genet 1999; 65: 1530–1537
   PubMedGoogle Scholar
• Ensembl [internet]. 2005. June–December—[cited 2006 March]; available from: http://www.ensembl.org/index.html.
   Google Scholar
• Aberdam D, Virolle T, Simon-Assmann P. Transcriptional regulation of laminin gene expression. Microsc Res Tech 2000; 51: 228–237
   PubMedGoogle Scholar
• Kleinman HK, Ebihara I, Killen PD, Sasaki M, Cannon FB, Yamada Y, Martin GR. Genes for basement membrane proteins are coordinately expressed in differentiating F9 cells but not in normal adult murine tissues. Dev Biol 1989; 122: 373–378
   Google Scholar
• Boylan JF, Lohnes D, Taneja R, ChaLBon P, Gudas LJ. Loss of retinoic acid receptor g function in F9 cells by gene disruption results in aberrant Hoxa-1 expression and differentiation upon retinoic acid treatment. Proc Natl Acad Sci 1993; 90: 9601–9605
   PubMedGoogle Scholar
• Faria TN, Mendelsohn C, ChaLBon P, Gudas LJ. The targeted disruption of both alleles of RARb(2) in F9 cells results in the loss of retinoic acid-associated growth arrest. J Biol Chem 1999; 274(26783)26788
   Google Scholar
• Chakrabarty S, Liu BR, Rajagopal S. Disruption of transforming growth factor beta-regulated laminin receptor function by expression of antisense laminin, a chain RNA in human colon cancer cells. J Cell Physiol 2001; 186: 47–52
   PubMedGoogle Scholar
• Palu E, Liesi P. Differential distribution of laminins in Alzheimer disease and normal human brain tissue. J Neurosci Res 2002; 69: 243–256
   PubMed Web of Science ®Google Scholar
• Voit T, Sewry CA, Meyer K, Hermann R, Straub V, Muntoni F, Kahn T, Unsold R, Helliwell TR, Appleton R, et al. Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker–Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy. Neuropediatrics 1995; 26(3)148–155, June
   PubMedGoogle Scholar
• McGrath JA, Kivirikko S, Ciatti S, Moss C, Christiano AM, Uitto J. A recurrent homozygous nonsense mutation within the LAMA3 gene as a cause of Herlitz junctional epidermolysis bullosa in patients of Pakistani ancestry: Evidence for a founder effect. J Invest Dermatol 1996; 106: 781–784
   PubMedGoogle Scholar
• Hirai Y, Utsugi K, Takeshima N, Kawamata Y, Furuta R, Kitagawa T, Hasumi K, Noda T. Putative gene loci associated with carcinogenesis and metastasis of endocervical adenocarcinomas of uterus determined by conventional and array-based CGH. Am J Obstet Gynecol 2004; 191: 1173–1182
   PubMed Web of Science ®Google Scholar
• Tiger CF, Champliaud MF, Pedrosa-Domellof F, Thornell LE, Ekblom P, Gullberg D. Presence of laminin alpha5 chain and lack of laminin alpha1 chain during human muscle development and in muscular dystrophies. J Biol Chem 1997; 272: 28590–28595
   PubMedGoogle Scholar
• Shen J, Li C, Gudas LJ. Regulation of the laminin beta 1 (LAMB1), retinoic acid receptor beta, and bone morphogenetic protein 2 genes in mutant F9 teratocarcinoma cell lines partially deficient in cyclic AMP-dependent protein kinase activity. Cell Growth Differ 1997; 8: 1297–1304
   PubMedGoogle Scholar
• Wewer UM, Durkin ME, Zhang X, Laursen H, Nielsen NH, Towfighi J, Engvall E, Albrechtsen R. Laminin beta 2 chain and adhalin deficiency in the skeletal muscle of Walker–Warburg syndrome (cerebro-ocular dysplasia-muscular dystrophy). Neurology 1995; 45: 2099–2101
   PubMedGoogle Scholar
• Muhle C, Jiang QJ, Charlesworth A, Bruckner-Tuderman L, Meneguzzi G, Schneider H. Novel and recurrent mutations in the laminin-5 genes causing lethal junctional epidermolysis bullosa: Molecular basis and clinical course of Herlitz disease. Hum Genet 2005; 116: 33–42
   PubMed Web of Science ®Google Scholar
• Gedde-Dahl T, Jr, Dupuy BM, Jonassen R, Winberg JO, Anton-Lamprecht I, Olaisen B. Junctional epidermolysis bullosa inversa (locus EBR2A) assigned to 1q31 by linkage and association to LAMC1. Hum Mol Genet 1994; 3: 1387–1391
   PubMedGoogle Scholar
• Castiglia D, Posteraro P, Spirito F, Pinola M, Angelo C, Puddu P, Meneguzzi G, Zambruno G. Novel mutations in the LAMC2 gene in non-Herlitz junctional epidermolysis bullosa: Effects on laminin-5 assembly, secretion, and deposition. J Invest Dermatol 2001; 117(3)731–739
   PubMedGoogle Scholar
• Amira N, Cancel-Tassin G, Bernardini S, Cochand-Priollet B, Bittard H, Mangin P, Fournier G, Latil A, Cussenot O. Expression in bladder transitional cell carcinoma by real-time quantitative reverse transcription polymerase chain reaction array of 65 genes at the tumor suppressor locus 9q34.1-2: Identification of 5 candidates tumor suppressor genes. Int J Cancer 2004; 111: 539–542
   PubMedGoogle Scholar
• Termaat RM, Assmann KJ, van Son JP, Dijkman HB, Koene RA, Berden JH. Antigen-specificity of antibodies bound to glomeruli of mice with systemic lupus erythematosus-like syndromes. Lab Invest 1993; 68: 164–173
   PubMedGoogle Scholar
• Kootstra CJ, Bergijk EC, Veninga A, Prins FA, de Heer E, Abrahamson DR, Bruijn JA. Qualitative alterations in laminin expression in experimental lupus nephritis. Am J Pathol 1995; 147: 476–488
   PubMedGoogle Scholar
• Peutz-Kootstra CJ, Hansen K, De Heer E, Abrass CK, Bruijn JA. Diferential expression of laminin chains and anti-laminin autoantibodies in experimental lupus nephritis. J Pathol 2000; 192: 404–412
   PubMedGoogle Scholar
• Ben-Yehuda A, Rasooly L, Bar-Tana R, Breuer G, Tadmor B, Ulmansky R, Naparstek Y. The urine of SLE patients contains antibodies that bind to the laminin component of the extracellular matrix. J Autoimmun 1995; 8: 279–291
   PubMed Web of Science ®Google Scholar
• Chan LS, Lapiere JC, Chen M, Traczyk T, Mancini AJ, Paller AS, Woodley DT, Marinkovich MP. Bullous systemic lupus erythematosus with autoantibodies recognizing multiple skin basement meLBrane components, bullous pemphigoid antigen 1, laminin-5, laminin-6, and type VII collagen. Arch Dermatol 1999; 135: 569–573
   PubMedGoogle Scholar
• Moser KL, Neas BR, Salmon JE, Yu H, Gray-Mcguire C, Asundi N, Bruner GR, Fox J, Kelly J, Henshall S, Bacino D, Dietz M, Hogue R, Koelsch G, Nightingale L, Shaver T, Abdou NI, Albert DA, Carson C, Petri M, Treadwell EL, James JA, Harley JB. Genome scan of human systemic lupus erythematosus: Evidence for linkage on chromosome 1q in African-American pedigrees. Proc Natl Acad Sci 1998; 95: 14869–14874
   PubMed Web of Science ®Google Scholar
• Lander E, Kruglyak L. Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results. Nature Genet 1995; 11: 241–247
   PubMed Web of Science ®Google Scholar
• Johanneson B, Lima G, Salomé J, Alarcón-Segovia D. A major susceptibility locus for systemic lupus erythemathosus maps to chromosome 1q31. Am J Hum Genet 2002; 71: 1060–1071
   PubMed Web of Science ®Google Scholar
• Ban Y, Tomer Y. The contribution of immune regulatory and thyroid specific genes to the etiology of Graves' and Hashimoto's diseases. Autoimmunity 2003; 36: 367–379
   PubMed Web of Science ®Google Scholar
• Martel P, Gilbert D, Drouot L, Prost C, Raux G, Delaporte E, Joly P, Tron F. A polymorphic variant of the gene coding desmoglein 1, the target autoantigen of pemphigus foliaceus, is associated with the disease. Genes Immun 2001; 2: 41–43
   PubMedGoogle Scholar
• Bain SC, Prins JB, Hearne CM, Rodrigues NR, Rowe BR, Pritchard LE, Ritchie RJ, Hall JRS, Undlien DE, Ronningen KS, Dunger DB, Barnett AH, Todd JA. Insulin gene region-encoded susceptibility to type 1 diabetes is not restricted to HLA − DR4 − positive individuals. Nature Genet 1992; 2: 212–215
   PubMedGoogle Scholar
• Perez P, Goicovich E, Alliende C, Aguilera S, Leyton C, Molina C, Pinto R, Romo R, Martinez B, Gonzalez MJ. Differential expression of matrix metalloproteinases in labial salivary glands of patients with primary Sjogren's syndrome. Arthritis Rheum 2000; 43: 2807–2817
   PubMed Web of Science ®Google Scholar
• Laine M, Virtanen I, Salo T, Konttinen YT. Segment-specific but pathologic laminin isoform profiles in human labial salivary glands of patients with Sjogren's syndrome. Arthritis Rheum 2004; 50: 3968–3973
   PubMedGoogle Scholar
• McArthur CP, Fox NW, Kragel P. Monoclonal antibody detection of laminin in minor salivary glands of patients with Sjogren's syndrome. J Autoimmun 1993; 6: 649–661
   PubMedGoogle Scholar
• McArthur CP, Daniels PJ, Kragel P, Howard PF, Julian L. Sjogren's syndrome salivary gland immunopathology: Increased laminin expression precedes lymphocytic infiltration. J Autoimmun 1997; 10: 59–65
   PubMedGoogle Scholar
• Molina C, Alliende C, Aguilera S, Kwon YJ, Leyton L, Martinez B, Leyton C, Perez P, Gonzalez MJ. Basal lamina disorganisation of the acini and ducts of labial salivary glands from patients with Sjogren's syndrome: Association with mononuclear cell infiltration. Ann Rheum Dis 2006; 65: 178–183
   PubMed Web of Science ®Google Scholar
• Goicovich E, Molina C, Perez P, Aguilera S, Fernandez J, Olea N, Alliende C, Leyton C, Romo R, Leyton L, Gonzalez MJ. Enhanced degradation of proteins of the basal lamina and stroma by matrix metalloproteinases from the salivary glands of Sjogren's syndrome patients: Correlation with reduced structural integrity of acini and ducts. Arthritis Rheum 2003; 48: 2573–2584
   PubMed Web of Science ®Google Scholar
• Perez P, Kwon YJ, Alliende C, Leyton L, Aguilera S, Molina C, et al. Increased acinar damage of salivary glands of patients with Sjogren's syndrome is paralleled by simultaneous imbalance of matrix metalloproteinase 3/tissue inhibitor of metalloproteinases 1 and matrix metalloproteinase 9/tissue inhibitor of metalloproteinases 1 ratios. Arthritis Rheum 2005; 52(9)2751–2760
   PubMedGoogle Scholar
• Kwon YJ, Pérez P, Aguilera S, Molina C, Leyton L, Alliende C, Leyton C, Brito M, Romo R, González MJ. Active remodeling of basal lamina from labial salivary glands of patients with Sjögren's syndrome involves specific laminins and nidogens. Arthritis Rheum, (in press)
   Google Scholar