HEREDITARY C6 DEFICIENCY IN A STRAIN OF PVG/C RATS

被引:0
|
作者
LEENAERTS, PL
STAD, RK
HALL, BM
VANDAMME, BJ
VANRENTERGHEM, Y
DAHA, MR
机构
[1] CATHOLIC UNIV LEUVEN,DEPT NEPHROL,B-3000 LOUVAIN,BELGIUM
[2] CATHOLIC UNIV LEUVEN,DEPT PATHOL,B-3000 LOUVAIN,BELGIUM
[3] LEIDEN UNIV HOSP,DEPT NEPHROL,2333 AA LEIDEN,NETHERLANDS
[4] ROYAL LIVERPOOL HOSP,DIV INTERNAL MED,SYDNEY,AUSTRALIA
来源
CLINICAL AND EXPERIMENTAL IMMUNOLOGY | 1994年 / 97卷 / 03期
关键词
C6; DEFICIENCY; PVG/C RAT; AUTOSOMAL RECESSIVE GENE;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A chance observation has led to the discovery of a strain of PVG rats (PVG/c(-)) which are deficient in complement (C) component C6. Analysis of total haemolytic activity (CH50) of PVG/c(-) serum revealed an absent CH50 activity compared with serum of other rat strains and of a PVG/c rat (PVG/c(+)) that showed normal C activity. Thus, the PVG/c(-) rat was unable to activate the C5b-9 membrane attack complex. To gain insight into the complement abnormalities, analysis of individual C components was performed. Testing the PVG/c(-) serum in a C6 haemolytic assay and using deficient human sera showed a deficiency of C6 in the PVG/c(-) rat. Highly purified human C6 and human sera deficient in other components were able to reconstitute the CH50 activity of the PVG/c(-) rat. The possibility that an inactivator of C was present in PVG/c(-) serum was excluded. The deficiency was found to be inheritable and under the control of an autosomal recessive gene. Furthermore, tissue antigens and immunity of the PVG/c(-) rat were found to be identical to those determined in the PVG/c(+) rat. With regard to their health status, the PVG/c(-) animals seem to have no disadvantages compared with PVG/c(+) rats when held under the same conditions within the protected environment of animal facilities. Taken together, both rat strains provide an unique animal model for studying the biological role of C, particularly the C5b-9 membrane attack complex in experimental medicine.
引用
收藏
页码:478 / 482
页数:5
相关论文
共 50 条
  • [31] PROLONGATION OF SURVIVAL OF DISCORDANT KIDNEY XENOGRAFTS BY C6 DEFICIENCY
    ZHOW, XJ
    NIESEN, N
    PAWLOWSKI, I
    BIESECKER, G
    ANDRES, G
    BRENTJENS, J
    MILGROM, F
    TRANSPLANTATION, 1990, 50 (05) : 896 - 898
  • [32] First reported complete C6 deficiency in Chinese patients
    Chiang, Valerie
    Wong, William
    Leung, Evelyn
    Au, Elaine
    Li, Philip
    JOURNAL OF CLINICAL IMMUNOLOGY, 2021, 41 (SUPPL 1) : S46 - S46
  • [33] HEREDITARY HYPER IGM ASSOCIATED WITH DECREASED C1Q, C6, AND C7
    MICHAEL, M
    FISCHER, T
    FORRISTAL, J
    WEST, C
    SWEENEY, J
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1987, 79 (01) : 228 - 228
  • [34] Coupling of the C6 and C6′ positions of sucrose by metathesis reaction
    Jarosz, S
    Listkowski, A
    Mach, M
    POLISH JOURNAL OF CHEMISTRY, 2001, 75 (05) : 683 - 687
  • [35] Patient with combined complement C6 and C7 deficiency, a case report
    Bouchard, Joelle
    Lavoie, Aubert
    Wagner, Eric
    Gauthier, Amelie
    JOURNAL OF CLINICAL IMMUNOLOGY, 2022, 42 (SUPPL 1) : S74 - S75
  • [36] Molecular defects leading to human complement component C6 deficiency (C6D).
    Zhu, ZB
    Totemchokchyakarn, K
    Atkinson, TP
    Whitley, RJ
    Volanakis, JE
    FASEB JOURNAL, 1996, 10 (06): : 2567 - 2567
  • [37] Recurrent meningococcal meningitis with complement 6 (C6) deficiency A case report
    Bae, Ji Yun
    Ham, Ahrong
    Choi, Hee Jung
    Kim, Chung-Jong
    MEDICINE, 2020, 99 (21) : E20362
  • [38] COMPLEMENT COMPONENT C6 AND C7 HAPLOTYPES ASSOCIATED WITH DEFICIENCIES OF C6
    FERNIE, BA
    ORREN, A
    WURZNER, R
    JONES, AM
    POTTER, PC
    LACHMANN, PJ
    HOBART, MJ
    ANNALS OF HUMAN GENETICS, 1995, 59 : 183 - 195
  • [39] PROPERTIES OF A LOW-MOLECULAR-WEIGHT COMPLEMENT COMPONENT C6 FOUND IN HUMAN-SUBJECTS WITH SUBTOTAL C6 DEFICIENCY
    ORREN, A
    WURZNER, R
    POTTER, PC
    FERNIE, BA
    COETZEE, S
    MORGAN, BP
    LACHMANN, PJ
    IMMUNOLOGY, 1992, 75 (01) : 10 - 16