IDENTIFICATION OF INTRAOCULAR-LENS ADSORBED PROTEINS IN MAMMALIAN IN-VITRO AND IN-VIVO SYSTEMS

被引:23
作者
KOCHOUNIAN, HH
KOVACS, SA
SY, J
GRUBBS, DE
MAXWELL, WA
机构
[1] CALIF STATE UNIV FRESNO, DEPT BIOL, FRESNO, CA 93740 USA
[2] CALIF STATE UNIV FRESNO, DEPT CHEM, FRESNO, CA 93740 USA
[3] UNIV CALIF SAN FRANCISCO, DEPT OPHTHALMOL, SAN FRANCISCO, CA 94143 USA
关键词
D O I
10.1001/archopht.1994.01090150125034
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Objective: Mammalian in vitro and in vivo systems were used to study the protein-adsorbing potential of intraocular lenses (IOLs). Methods: Intraocular lenses composed of polymethyl methacrylate optics with polypropylene haptics were incubated in rabbit plasma for 3 hours (in vitro grouping) or implanted in rabbit eyes for 48 hours (in vivo grouping). Lens-adsorbed proteins from both experimental groupings were eluted with sodium dodecyl sulfate and identified by Western Blot analyses. Results: The adsorbed protein layer was composed of at least six different proteins, albumin, complement C3 fragments, IgG, fibrinogen/fibrin (as a fibrin clot in vivo), fibronectin, and transferrin. Of the identified components, albumin, IgG, fibronectin, and fibrinogen were the predominant protein species on the in vitro IOLs, while fibronectin and fibrin were on the in vivo IOLs. Conclusions: The composition of the protein layer has the potential to alter the biological property of IOLs.
引用
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页码:395 / 401
页数:7
相关论文
共 54 条
  • [1] AKIYAMA SK, 1987, ADV ENZYMOL RAMB, V59, P1
  • [2] COMPLICATIONS OF INTRAOCULAR LENSES - A HISTORICAL AND HISTOPATHOLOGICAL REVIEW
    APPLE, DJ
    MAMALIS, N
    LOFTFIELD, K
    GOOGE, JM
    NOVAK, LC
    KAVKAVANNORMAN, D
    BRADY, SE
    OLSON, RJ
    [J]. SURVEY OF OPHTHALMOLOGY, 1984, 29 (01) : 1 - 54
  • [3] Baier R E, 1969, J Biomed Mater Res, V3, P191, DOI 10.1002/jbm.820030115
  • [4] ORGANIZATION OF BLOOD COMPONENTS NEAR INTERFACES
    BAIER, RE
    [J]. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1977, 283 (FEB10) : 17 - 36
  • [5] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [6] Brash J.L., 1983, BIOCOMPATIBLE POLYM, P35
  • [7] ANALYSIS OF THE COMPLEMENT C-3 FRAGMENTS ASSOCIATED WITH HEMODIALYSIS MEMBRANES
    CHEUNG, AK
    PARKER, CJ
    JANATOVA, J
    [J]. KIDNEY INTERNATIONAL, 1989, 35 (02) : 576 - 588
  • [8] INITIATION OF BLOOD-COAGULATION AT ARTIFICIAL SURFACES
    COLMAN, RW
    SCOTT, CF
    SCHMAIER, AH
    WACHTFOGEL, YT
    PIXLEY, RA
    EDMUNDS, LH
    [J]. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1987, 516 : 253 - 267
  • [9] HEMODIALYSIS LEUKOPENIA - PULMONARY VASCULAR LEUKOSTASIS RESULTING FROM COMPLEMENT ACTIVATION BY DIALYZER CELLOPHANE MEMBRANES
    CRADDOCK, PR
    FEHR, J
    DALMASSO, AP
    BRIGHAM, KL
    JACOB, HS
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1977, 59 (05) : 879 - 888
  • [10] BIOTINYLATED PROTEINS AS MOLECULAR-WEIGHT STANDARDS ON WESTERN BLOTS
    DELLAPENNA, D
    CHRISTOFFERSEN, RE
    BENNETT, AB
    [J]. ANALYTICAL BIOCHEMISTRY, 1986, 152 (02) : 329 - 332