Zusammenfassung
Das retinale Pigmentepithel (PRE) grenzt mit seiner Basalmembran an die Bruch-Membran und Kapillaren der Aderhaut (Choriokapillaris ). Apikal steht es mit seinen Mikrowellen in engem Kontakt zu den Photorezeptoraußensegmenten. In einem komplizierten Stoffwechselaustausch zwischen Netzhaut und Aderhaut kommt dem RPE eine Schlüsselfunktion zu. Neben der Aufbereitung des Sehpigments im Sehzyklus werden die Membranscheiben der Photorezeptoraußensegmente durch die RPE-Zelle phagozytiert und in Richtung Choriokapillaris abgegeben. Weiterhin reguliert die Pumpfunktion des RPE das extrazelluläre Ionenmillieu der Photorezeptoren. Ein auf diese Weise erzeugter osmotischer Unterdruck sorgt gleichfalls auch für eine Adhäsion der Netzhaut am RPE und ist ein wichtiger Bestandteil zur Verhinderung von Netzhautablösungen. Produktion und Sekretion verschiedener Wachstumsfaktoren reguliert das Milieu für die Aufrechterhaltung der funktionellen Einheit aus Photorezeptoren, RPE und Choriokapillaris.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Literatur
[No authors listed] (1991) Subfoveal neovascular lesions in age-related macular degeneration. Guidelines for evaluation and treatment in the macular photocoagulation study. Macular Photocoagulation Study Group. Archives of ophthalmology 109: 1242–1257
Ahir A, Guo L, Hussain AA, Marshall J (2002) Expression of metalloproteinases from human retinal pigment epithelial cells and their effects on the hydraulic conductivity of Bruch’s membrane. Investigative ophthalmology & visual science 43: 458–465
Aisenbrey S, Zhang M, Bacher D, Yee J, Brunken WJ, Hunter DD (2006) Retinal pigment epithelial cells synthesize laminins, including laminin 5, and adhere to them through alpha3- and alpha6-containing integrins. Investigative ophthalmology & visual science 47: 5537–5544
Archer DB, Gardiner TA (1981a) Electron microscopic features of experimental choroidal neovascularization. American journal of ophthalmology 91: 433–457
Archer DB, Gardiner TA (1981b) Morphologic fluorescein angiographic, and light microscopic features of experimental choroidal neovascularization. American journal of ophthalmology 91: 297–311
Arroyo JG, Yang L, Bula D. Chen DF (2005) Photoreceptor apoptosis in human retinal detachment. American journal of ophthalmology 139: 605–610
Bairati A, Jr, Orzalesi N (1963) The Ultrastructure of the Pigment Epithelium and of the Photoreceptor-Pigment Epithelium Junction in the Human Retina. Journal of ultrastructure research 41: 484–496
Barondes M, Pauleikhoff D, Chisholm IC, Minassian D, Bird AC (1990) Bilaterality of drusen. The British journal of ophthalmology 74: 180–182
Barondes MJ, Pagliarini S, Chisholm IH, Hamilton AM, Bird AC (1992) Controlled trial of laser photocoagulation of pigment epithelial detachments in the elderly: 4 year review. The British journal of ophthalmology 76: 5–7
Bird AC (1991) Doyne Lecture. Pathogenesis of retinal pigment epithelial detachment in the elderly; the relevance of Bruch’s membrane change. Eye (London, England) 5 (Pt 1): 1–12
Bird AC (1993) Choroidal neovascularisation in age-related macular disease. The British journal of ophthalmology 77: 614–615
Bird AC, Marshall J (1986) Retinal pigment epithelial detachments in the elderly. Transactions of the ophthalmological societies of the United Kingdom 105 (Pt 6): 674–682
Bok D (1985) Retinal photoreceptor-pigment epithelium interactions. Friedenwald lecture. Investigative ophthalmology & visual science 26: 1659–1694
Bressler NM, Bressler SB, Fine SL (1988a) Age-related macular degeneration. Survey of ophthalmology 32: 375–413
Bressler NM, Bressler SB, Gragoudas ES (1987) Clinical characteristics of choroidal neovascular membranes. Archives of ophthalmology 105. 209–213
Bressler NM, Bressler SB, Seddon JM; Gragoudas ES Jacobson LP (1988b) Drusen characteristics in patients with exudative versus non-exudative age-related macular degeneration. Retina (Philadelphia, Pa) 8: 109–114
Burns RP, Feeney-Burns L (1980) Clinico-morphologic correlations of drusen of Bruch’s membrane. Transactions of the American Ophthalmological Society 78: 206–225
Campochiaro PA, Jerdon JA, Glaser BM (1986) The extracellular matrix of human retinal pigment epithelial cells in vivo and its synthesis in vitro. Investigative ophthalmology & visual science 27: 1615–1621
Capon MR, Marshall J, Krafft JI, Alexander RA, Hiscott PS, Bird AC (1989) Sorsby’s fundus dystrophy. A light and electron microscopic study. Ophthalmology 96: 1769–1777
Casswell AG, Kohen D, Bird AC (1985) Retinal pigment epithelial detachments in the elderly: classification and outcome. The British journal of ophthalmology 69: 397–403
Chang CJ, Lai WW, Edward DP, Tso MO (1995) Apoptotic photoreceptor cell death after traumatic retinal detachment in humans. Archives of ophthalmology 113: 880–886
Chen JC, Fitzke FW, Pauleikhoff D, Bird AC (1992) Functional loss in age-related Bruch’s membrane change with choroidal perfusion defect. Investigative ophthalmology & visual science 33: 334–340
Chuang EL, Bird AC (1988) The pathogenesis of tears of the retinal pigment epithelium. American journal of ophthalmology 105: 285–290
Coffey AJ, Brownstein S (1986) The prevalence of macular drusen in postmortem eyes. American journal of ophthalmology 102: 164–171
Curcio CA, Johnson M, Huang JD, Rudolf M (2009) Aging, agerelated macular degeneration, and the response-to-retention of apolipoprotein B-containing lipoproteins. Progress in retinal and eye research 28: 393–422
Curcio CA, Millican CL (1999) Basal linear deposit and large drusen are specific for early age-related maculopathy. Archives of ophthalmology 117: 329–339
Curcio CA, Millican CL, Bailey T, Kruth HS (2001) Accumulation of cholesterol with age in human Bruch’s membrane. Investigative ophthalmology & visual science 42: 265–274
Curcio CA, Presley JB, Malek G, Medeiros NE, Avery DV, Kruth HS (2005) Esterified and unesterified cholesterol in drusen and basal deposits of eyes with age-related maculopathy. Experimental eye research 81: 731–741
Dastgheib K, Green WR (1994) Granulomatous reaction to Bruch’s membrane in age-related macular degeneration. Archives of ophthalmology 112: 813–818
Davis WL, Jones RG, Hagler HK (1981) An electron microscopic histochemical and analytical X-ray microprobe study of calcification in Bruch’s membrane from human eyes. J Histochem Cytochem 29: 601–608
Delori FC, Dorey CK, Staurenghi G, Arend O, Goger DG, Weiter JJ (1995) In vivo fluorescence of the ocular fundus exhibits retinal pigment epithelium lipofuscin characteristics. Investigative ophthalmology & visual science 36: 718–729
Dithmar S, Sharara NA, Curcio CA, Le NA, Zhang Y, Brown S, Grossniklaus HE (2001) Murine high-fat diet and laser photochemical model of basal deposits in Bruch membrane. Archives of ophthalmology 119: 1643–1649
Dorey CK, Wu G, Ebenstein D, Garsd A, Weiter JJ (1989) Cell loss in the aging retina. Relationship to lipofuscin accumulation and macular degeneration. Investigative ophthalmology & visual science 30: 1691–1699
Farkas TG, Sylvester V, Archer D (1971) The ultrastructure of drusen. American journal of ophthalmology 71: 1196–1205
Feeney-Burns L, Ellersieck MR (1985) Age-related changes in the ultrastructure of Bruch’s membrane. American journal of ophthalmology 100: 686–697
Fisher RF (1982) The water permeability of basement membrane under increasing pressure: evidence for a new theory of permeability. Proceedings of the Royal Society of London. Series B, Containing papers of a Biological character 216: 475–496
Fisher RF (1987) The influence of age on some ocular basement membranes. Eye (London, England) 1 (Pt 2): 184–189
Foulds WS (1976) Doyne Memorial Lecture 1976. Clinical significance of trans-scleral fluid transfer. Transactions of the ophthalmological societies of the United Kingdom 96: 290–308
Gamulescu MA, Renner AB, Helbig H (2009) [Clinical manifestations of functional disturbances of the retinal pigment epithelium]. Ophthalmologe 106: 305–310
Gass JD (1967) Pathogenesis of disciform detachment of the neuroepithelium. American journal of ophthalmology 63: Suppl:1–139
Gass JD (1973) Drusen and disciform macular detachment and degeneration. Archives of ophthalmology 90: 206–217
Gass JD (1984) Pathogenesis of tears of the retinal pigment epithelium. The British journal of ophthalmology 68: 513–519
Green WR, Enger C (1993) Age-related macular degeneration histopathologic studies. The 1992 Lorenz E. Zimmerman Lecture. Ophthalmology 100: 1519–1535
Green WR, Key SN, 3rd (1977) Senile macular degeneration: a histopathologic study. Transactions of the American Ophthalmological Society 75: 180–254
Green WR, McDonnell PJ, Yeo JH (1985) Pathologic features of senile macular degeneration. Ophthalmology 92: 615–627
Grossniklaus HE, Gass JD (1998) Clinicopathologic correlations of surgically excised type 1 and type 2 submacular choroidal neovascular membranes. American journal of ophthalmology 126: 59–69
Grossniklaus HE, Green WR (1998) Histopathologic and ultrastructural findings of surgically excised choroidal neovascularization. Submacular Surgery Trials Research Group. Archives of ophthalmology 116: 745–749
Grossniklaus HE, Hutchinson AK, Capone A, Jr, Woolfson J, Lambert HM (1994) Clinicopathologic features of surgically excised choroidal neovascular membranes. Ophthalmology 101: 1099–1111
Guo L, Hussain AA, Limb GA, Marshall J (1999) Age-dependent variation in metalloproteinase activity of isolated human Bruch’s membrane and choroid. Investigative ophthalmology & visual science 40: 2676–2682
Guymer R, Luthert P, Bird A (1999) Changes in Bruch’s membrane and related structures with age. Progress in retinal and eye research 18: 59–90
Haimovici R, Gantz DL, Rumelt S, Freddo TF, Small DM (2001) The lipid composition of drusen, Bruch’s membrane, and sclera by hot stage polarizing light microscopy. Investigative ophthalmology & visual science 42: 1592–1599
Hamlin CR, Kohn RR (1971) Evidence for progressive, age-related structural changes in post–mature human collagen. Biochimica et biophysica acta 236: 458–467
Handa JT, Verzijl N, Matsunaga H, Aotaki-Keen A, Lutty GA, te Koppele JM, Miyata T, Hjelmeland LM (1999) Increase in the advanced glycation end product pentosidine in Bruch’s membrane with age. Investigative ophthalmology & visual science 40: 775–779
Hao W, Wenzel A, Obin MS, Chen CK, Brill E, Krasnoperova NV, Eversole-Cire P, Kleyner Y, Taylor A, Simon MI, et al: (2002) Evidence for two apoptotic pathways in light-induced retinal degeneration. Nature genetics 32: 254–260
Hermans P, Lommatzsch A, Bomfeld N, Pauleikhoff D (2003) [Angiographic-histological correlation of late exudative agerelated macular degeneration]. Ophthalmologe 100: 378–383
Ho TC, Del Priore LV (1997) Reattachment of cultured human retinal pigment epithelium to extracellular matrix and human Bruch’s membrane. Investigative ophthalmology & visual science 38: 1110–1118
Hogan MJ (1965) Macular Diseases: Pathogenesis. Electron Microscopy of Bruch’s Membrane. Transactions – American Academy of Ophthalmology and Otolaryngology 69: 683–690
Holz FG, Sheraidah G, Pauleikhoff D, Bird AC (1994) Analysis of lipid deposits extracted from human macular and peripheral Bruch’s membrane. Archives of ophthalmology 112: 402–406
Howard EW, Benton R, Ahern-Moore J, Tomasek JJ (1996) Cellular contraction of collagen lattices is inhibited by nonenzymatic glycation. Experimental cell research 228: 132–137
Huang JD, Presley JB, Chimento MF, Curcio CA, Johnson M (2007) Age-related changes in human macular Bruch’s membrane as seen by quick-freeze/deep-etch. Experimental eye research 85. 202–218
Hussain AA, Rowe L, Marshall J (2002) Age-related alterations in the diffusional transport of amino acids across the human Bruch’s-choroid complex. Journal of the Optical Society of America 19: 166–172
Hyman L, Schachat AP, He Q, Leske MC (2000) Hypertension, cardiovascular disease, and age-related macular degeneration. Age-Related Macular Degeneration Risk Factors Study Group. Archives of ophthalmology 118: 351–358
Ishibashi T, Murata T, Hangai M, Nagai R, Horiuchi S, Lopez PF, Hinton DR, Ryan SJ (1998) Advanced glycation end products in age-related macular degeneration. Archives of ophthalmology 116: 1629–1632
Ishibashi T, Patterson R, Ohnishi Y, Inomata H, Ryan SJ (1986a) Formation of drusen in the human eye. American journal of ophthalmology 101: 342–353
Ishibashi T, Sorgente N, Patterson R, Ryan SJ (1986b) Pathogenesis of drusen in the primate. Investigative ophthalmology & visual science 27: 184–193
Johnson M, Dabholkar A, Huang JD, Presley JB, Chimento MF, Curcio CA (2007) Comparison of morphology of human macular and peripheral Bruch’s membrane in older eyes. Current eye research 32: 791–799
Kamei M, Hollyfield JG (1999) TIMP-3 in Bruch’s membrane: changes during aging and in age-related macular degeneration. Investigative ophthalmology & visual science 40: 2367–2375
Karwatowski WS, Jeffries TE, Duance VC, Albon J, Bailey AJ, Easty DL (1995) Preparation of Bruch’s membrane and analysis of the age-related changes in the structural collagens. The British journal of ophthalmology 79: 944–952
Killingsworth MC, Sarks JP, Sarks SH (1990) Macrophages related to Bruch’s membrane in age-related macular degeneration. Eye (London, England) 4 (Pt 4): 613–621
Kliffen M, Mooy CM, Luider TM, de Jong PT (1994) Analysis of carbohydrate structures in basal laminar deposit in aging human maculae. Investigative ophthalmology & visual science 35: 2901–2905
Kliffen M, Mooy CM, Luider TM, Huijmans JG, Kerkvliet S, de Jong PT (1996) Identification of glycosaminoglycans in agerelated macular deposits. Archives of ophthalmology 114: 1009–1014
Krishnamurti U, Rondeau E, Sraer JD, Michael AF, Tsilibary EC (1997) Alterations in human glomerular epithelial cells interacting with nonenzymatically glycosylated matrix. The Journal of biological chemistry 272: 27966–27970
Kunze A, Abari E, Semkova I, Paulsson M, Hartmann U (2009) Deposition of nidogens and other basement membrane proteins in the young and aging mouse retina. Ophthalmic research 43: 108–112
Lafaut BA, Aisenbrey S, Van den Broecke C, Krott R, Jonescu-Cuypers CP, Reynders S, Bartz-Schmidt KU (2001) Clinicopathological correlation of retinal pigment epithelial tears in exudative age related macular degeneration: pretear, tear, and scarred tear. The British journal of ophthalmology 85: 454–460
Loffler KU, Lee WR (1986) Basal linear deposit in the human macula Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 224: 493–501
Lommatzsch A, Heimes B, Gutfleisch M, Spital G, Zeimer M, Pauleikhoff D (2009) Serous pigment epithelial detachment in age-related macular degeneration: comparison of different treatments. Eye (London, England) 23: 2163–2168
Lommatzsch A, Hermans P, Muller KD, Bornfeld N, Bird AC, Pauleikhoff D (2008) Are low inflammatory reactions involved in exudative age-related macular degeneration? Morphological and immunhistochemical analysis of AMD associated with basal deposits. Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 246: 803–810
Marshall GE, Konstas AG, Reid GG, Edwards JG, Lee WR (1994) Collagens in the aged human macula. Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 232: 133–140
Marshall J (1987) The ageing retina: physiology or pathology. Eye (London, England) 1 (Pt 2): 282–295
Marshall J, Hussain AA, Starita C, Moore DJ, Patmore AL (1998) Aging and Bruch’s Membrane: In: Marmor MF, Wolfensberger TJ (eds) The Retinal Pigment Epithelium: Function and Disease. Oxford University Press, pp. 669–692
Martinez GS, Campbell AJ, Reinken J, Allan BC (1982) Prevalence of ocular disease in a population study of subjects 65 years old and older. American journal of ophthalmology 94: 181–189
Miller H, Miller B, Ryan SJ (1986a) Newly-formed subretinal vessels. Fine structure and fluorescein leakage. Investigative ophthalmology & visual science 27. 204–213
Miller H, Miller B, Ryan SJ (1986b) The role of retinal pigment epithelium in the involution of subretinal neovascularization. Investigative ophthalmology & visual science 27: 1644–1652
Moore DJ, Hussain AA, Marshall J (1995) Age-related variation in the hydraulic conductivity of Bruch’s membrane. Investigative ophthalmology & visual science 36: 1290–1297
Mullins RF, Aptsiauri N, Hageman, GS (2001) Structure and composition of drusen associated with glomerulonephritis: implications for the role of complement activation in drusen biogenesis. Eye (London, England) 15: 390–395
Mullins RF, Johnson LV, Anderson DH, Hageman GS (1997) Characterization of drusen-associated glycoconjugates. Ophthalmology 104: 288–294
Mullins RF, Russell SR, Anderson DH, Hageman GS (2000) Drusen associated with aging and age-related macular degeneration contain proteins common to extracellular deposits associated with atherosclerosis, elastosis, amyloidosis, and dense deposit disease. Faseb J 14: 835–846
Nakaizumi Y, Hogan MJ, Feeney L (1964) The Ultrastructure of Bruch’s Membrane. 3. the Macular Area of the Human Eye. Archives of ophthalmology 72: 395–400
Neuner B, Wellmann J, Dasch B, Behrens T, Claes B, Dietzel M, Pauleikhoff D, Hense HW (2007) Modeling smoking history: a comparison of different approaches in the MARS study on agerelated maculopathy. Annals of epidemiology 17: 615–621
Okubo A, Rosa RH, Jr, Bunce CV, Alexander RA, Fan JT, Bird AC, Luthert PJ (1999) The relationships of age changes in retinal pigment epithelium and Bruch’s membrane. Investigative ophthalmology & visual science 40: 443–449
Pauleikhoff D, Chen J, Bird AC, Wessing A (1992a) [The Bruch membrane and choroid Angiography and functional characteristics in age-related changes]. Ophthalmologe 89: 39–44
Pauleikhoff D, Harper CA, Marshall J, Bird AC (1990) Aging changes in Bruch’s membrane A histochemical and morphologic study. Ophthalmology 97: 171–178
Pauleikhoff D, Koch JM (1995) Prevalence of age-related macular degeneration. Current opinion in ophthalmology 6: 51–56
Pauleikhoff D, Loffert D, Spital G, Radermacher M, Dohrmann J, Lommatzsch A, Bird AC (2002) Pigment epithelial detachment in the elderly. Clinical differentiation, natural course and pathogenetic implications. Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 240: 533–538
Pauleikhoff D, Sheraidah G, Marshall J, Bird AC, Wessing A (1994) [Biochemical and histochemical analysis of age related lipid deposits in Bruch’s membrane]. Ophthalmologe 91: 730–734
Pauleikhoff D, Wojteki S, Muller D, Bornfeld N, Heiligenhaus A (2000) [Adhesive properties of basal membranes of Bruch’s membrane. Immunohistochemical studies of age-dependent changes in adhesive molecules and lipid deposits]. Ophthalmologe 97: 243–250
Pauleikhoff D, Zuels S, Sheraidah GS, Marshall J, Wessing A, Bird AC (1992b) Correlation between biochemical composition and fluorescein binding of deposits in Bruch’s membrane. Ophthalmology 99: 1548–1553
Penfold PL, Killingsworth MC, Sarks SH (1985) Senile macular degeneration: the involvement of immunocompetent cells. Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 223: 69–76
Penfold PL, Liew SC, Madigan MC, Provis JM (1997) Modulation of major histocompatibility complex class II expression in retinas with age-related macular degeneration. Investigative ophthalmology & visual science 38: 2125–2133
Penfold PL, Madigan MC, Gillies MC, Provis JM (2001) Immunological and aetiological aspects of macular degeneration. Progress in retinal and eye research 20: 385–414
Ramrattan RS, Van Der Schaft TL, Mooy CM, de Bruijn WC, Mulder PG, de Jong PT (1994) Morphometric analysis of Bruch’s membrane, the choriocapillaris, and the choroid in aging. Investigative ophthalmology & visual science 35: 2857–2864
Rittie L, Berton A, Monboisse JC, Hornebeck W, Gillery P (1999) Decreased contraction of glycated collagen lattices coincides with impaired matrix metalloproteinase production. Biochemical and biophysical research communications 264: 488–492
Rizzolo LJ (1991) Basement membrane stimulates the polarized distribution of integrins but not the Na,K-ATPase in the retinal pigment epithelium. Cell regulation 2: 939–949
Sarks JP, Sarks SH, Killingsworth MC (1988) Evolution of geographic atrophy of the retinal pigment epithelium. Eye (London, England) 2 (Pt 5): 552–577
Sarks SH (1976) Ageing and degeneration in the macular region: a clinico-pathological study. The British journal of ophthalmology 60: 324–341
Sarks SH, Van Driel D, Maxwell L, Killingsworth M (1980) Softening of drusen and subretinal neovascularization. Transactions of the ophthalmological societies of the United Kingdom 100: 414–422
Sheraidah G, Steinmetz R, Maguire J, Pauleikhoff D, Marshall J, Bird AC (1993) Correlation between lipids extracted from Bruch’s membrane and age. Ophthalmology 100: 47–51
Soubrane G, Coscas G, Francais C, Koenig F (1990) Occult subretinal new vessels in age-related macular degeneration. Natural History and early laser treatment. Ophthalmology 97: 649–657
Spaide RF, Ho-Spaide WC, Browne RW, Armstrong D (1999) Characterization of peroxidized lipids in Bruch’s membrane. Retina (Philadelphia, Pa) 19: 141–147
Spraul CW, Lang GE, Grossniklaus HE, Lang GK (1998) [Characteristics of drusen and changes in Bruch’s membrane in eyes with age-related macular degeneration. Histological study]. Ophthalmologe 95: 73–79
Starita C, Hussain AA, Marshall J (1995) Decreasing hydraulic conductivity of Bruch’s membrane: relevance to photoreceptor survival and lipofuscinoses. American journal of medical genetics 57: 235–237
Starita C, Hussain AA, Pagliarini S, Marshall J (1996) Hydrodynamics of ageing Bruch’s membrane: implications for macular disease. Experimental eye research 62: 565–572
Starita C, Hussain AA, Patmore A, Marshall J (1997) Localization of the site of major resistance to fluid transport in Bruch’s membrane. Investigative ophthalmology & visual science 38: 762–767
Strauss O (2005) The retinal pigment epithelium in visual function. Physiological reviews 85: 845–881
Strauss O (2009) [The role of retinal pigment epithelium in visual functions]. Ophthalmologe 106: 299–304
Tian SF, Toda S, Higashino H, Matsumura S (1996) Glycation decreases the stability of the triple-helical strands of fibrous collagen against proteolytic degradation by pepsin in a specific temperature range. Journal of biochemistry 120: 1153–1162
Tsuboi S (1987) Measurement of the volume flow and hydraulic conductivity across the isolated dog retinal pigment epithelium. Investigative ophthalmology & visual science 28: 1776–1782
Van Der Schaft TL, de Bruijn WC, Mooy CM, Ketelaars DA, de Jong PT (1991) Is basal laminar deposit unique for age-related macular degeneration? Archives of ophthalmology 109: 420–425
Van Der Schaft TL, Mooy CM, de Bruijn WC, Bosman FT, de Jong PT (1994) Immunohistochemical light and electron microscopy of basal laminar deposit. Graefe’s archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 232: 40–46
Vater CA, Harris ED, Jr, Siegel RC (1979) Native cross-links in collagen fibrils induce resistance to human synovial collagenase. The Biochemical journal 181: 639–645
Wang L, Li CM, Rudolf M, Belyaeva OV, Chung BH, Messinger JD, Kedishvili NY, Curcio CA (2009) Lipoprotein particles of intraocular origin in human Bruch membrane: an unusual lipid profile. Investigative ophthalmology & visual science 50: 870–877
Wasmuth S, Lueck K, Baehler H, Lommatzsch A, Pauleikhoff D (2009) Increased vitronectin production by complementstimulated human retinal pigment epithelial cells. Investigative ophthalmology & visual science 50: 5304–5309
Wimmers S, Karl MO, Strauss O (2007) Ion channels in the RPE. Progress in retinal and eye research 26: 263–301
Young RW (1987) Pathophysiology of age-related macular degeneration. Survey of ophthalmology 31: 291–306
Zacks DN, Zheng QD, Han Y, Bakhru R, Miller JW (2004) FAS-mediated apoptosis and its relation to intrinsic pathway activation in an experimental model of retinal detachment. Investigative ophthalmology & visual science 45: 4563–4569
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 2011 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Lommatzsch, A., Wasmuth, S., Pauleikhoff, D., Holz, F.G., Bird, A.C. (2011). Histopathologie. In: Altersabhängige Makuladegeneration. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-20870-6_5
Download citation
DOI: https://doi.org/10.1007/978-3-642-20870-6_5
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-20869-0
Online ISBN: 978-3-642-20870-6
eBook Packages: Medicine (German Language)