FORMALDEHYDE TREATED ALBUMIN CONTAINS MONOMERIC AND POLYMERIC FORMS THAT ARE DIFFERENTLY CLEARED BY ENDOTHELIAL AND KUPFFER CELLS OF THE LIVER - EVIDENCE FOR SCAVENGER RECEPTOR HETEROGENEITY

被引:47
作者
JANSEN, RW
MOLEMA, G
HARMS, G
KRUIJT, JK
VANBERKEL, TJC
HARDONK, MJ
MEIJER, DKF
机构
[1] LEIDEN UNIV,CTR BIOPHARMACEUT SCI,DIV BIOPHARMACEUT,2300 RA LEIDEN,NETHERLANDS
[2] STATE UNIV GRONINGEN,DEPT PATHOL,9713 AW GRONINGEN,NETHERLANDS
关键词
D O I
10.1016/S0006-291X(05)81249-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Formaldehyde treated albumin (F-HSA) was found to consist of a monomeric and a polymeric fraction. Both fractions were primarily endocytosed by rat liver sinusoidal cells. However, immunohistochemical staining of endocytosed material showed that the relative contribution of the endothelial and Kupffer cells in uptake of the monomer and the polymer differed significantly, with the monomer mainly having an endothelial cell- and the polymer predominantly having a Kupffer cell pattern of distribution. To directly confirm these heterogeneous patterns, we injected in vivo the 125I-labeled F-HSA fractions and isolated the endothelial and Kupffer cells by centrifugal elutriation. 73.7% of the monomeric F-HSA was found in endothelial cells and only 14.9% was found in Kupffer cells. In contrast, the polymeric F-HSA (1500 kD) was mainly endocytosed by Kupffer cells (71%), whereas the endothelial cells contributed only for 24% in hepatic uptake. In vivo studies and isolated perfused rat liver experiments showed that endocytosis of both monomer and polymer was inhibited by co-administration of polyinosinic acid, a well known inhibitor for scavenger receptors, indicating that these receptors on endothelial and Kupffer cells are mainly involved in this uptake process. © 1991 Academic Press, Inc.
引用
收藏
页码:23 / 32
页数:10
相关论文
共 24 条
[1]   ENDOCYTOSIS OF FORMALDEHYDE-TREATED SERUM-ALBUMIN VIA SCAVENGER PATHWAY IN LIVER ENDOTHELIAL-CELLS [J].
BLOMHOFF, R ;
ESKILD, W ;
BERG, T .
BIOCHEMICAL JOURNAL, 1984, 218 (01) :81-86
[2]  
BUYS CHC, 1974, BIOCHIM BIOPHYS ACTA, V392, P95
[3]  
BUYS CHCM, 1973, J RETICULOENDOTH SOC, V14, P209
[4]   INTRACELLULAR-TRANSPORT OF FORMALDEHYDE-TREATED SERUM-ALBUMIN IN LIVER ENDOTHELIAL-CELLS AFTER UPTAKE VIA SCAVENGER RECEPTORS [J].
ESKILD, W ;
KINDBERG, GM ;
SMEDSROD, B ;
BLOMHOFF, R ;
NORUM, KR ;
BERG, T .
BIOCHEMICAL JOURNAL, 1989, 258 (02) :511-520
[5]   REACTION OF PROTEINS WITH FORMALDEHYDE IN PRESENCE AND ABSENCE OF SODIUM-BOROHYDRIDE [J].
GALEMBECK, F ;
RYAN, DS ;
WHITAKER, JR ;
FEENEY, RE .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1977, 25 (02) :238-245
[6]   BINDING-SITE ON MACROPHAGES THAT MEDIATES UPTAKE AND DEGRADATION OF ACETYLATED LOW-DENSITY LIPOPROTEIN, PRODUCING MASSIVE CHOLESTEROL DEPOSITION [J].
GOLDSTEIN, JL ;
HO, YK ;
BASU, SK ;
BROWN, MS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (01) :333-337
[7]   PREPARATION OF 131I-LABELLED HUMAN GROWTH HORMONE OF HIGH SPECIFIC RADIOACTIVITY [J].
GREENWOOD, FC ;
HUNTER, WM .
BIOCHEMICAL JOURNAL, 1963, 89 (01) :114-&
[8]   DETERMINATION OF FREE AMINO GROUPS IN PROTEINS BY TRINITROBENZENESULFONIC ACID [J].
HABEEB, AFS .
ANALYTICAL BIOCHEMISTRY, 1966, 14 (03) :328-&
[9]   GLYCOSYL RECEPTORS IN MACROPHAGE SUBPOPULATIONS OF RAT SPLEEN AND LYMPH-NODE - A COMPARATIVE-STUDY USING NEOGLYCOPROTEINS AND MONOCLONAL-ANTIBODIES ED1, ED2 AND ED3 [J].
HARMS, G ;
DIJKSTRA, CD ;
HARDONK, MJ .
CELL AND TISSUE RESEARCH, 1990, 262 (01) :35-40
[10]  
HORIUCHI S, 1985, J BIOL CHEM, V260, P475