MYELIN PROTEOLIPID PROTEIN - MINIMUM SEQUENCE REQUIREMENTS FOR ACTIVE INDUCTION OF AUTOIMMUNE ENCEPHALOMYELITIS IN SWR/J AND SJL/J MICE

被引:54
作者
TUOHY, VK
SOBEL, RA
LU, ZJ
LAURSEN, RA
LEES, MB
机构
[1] EK SHRIVER CTR,DEPT BIOCHEM,WALTHAM,MA
[2] BOSTON UNIV,DEPT CHEM,BOSTON,MA 02215
[3] MASSACHUSETTS GEN HOSP,NEUROL SERV,BOSTON,MA 02114
[4] MASSACHUSETTS GEN HOSP,IMMUNOPATHOL UNIT,BOSTON,MA 02114
[5] MASSACHUSETTS GEN HOSP,NEUROPATHOL UNIT,BOSTON,MA 02114
[6] HARVARD UNIV,SCH MED,DEPT NEUROL,BOSTON,MA 02115
[7] HARVARD UNIV,SCH MED,DEPT PATHOL,BOSTON,MA 02115
关键词
MYELIN PROTEOLIPID PROTEIN; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; T-CELL EPITOPE; ENCEPHALITOGENIC; DEMYELINATION; MULTIPLE SCLEROSIS;
D O I
10.1016/0165-5728(92)90175-K
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Proteolipid protein (PLP) is the major protein constituent of mammalian central nervous system myelin. We have previously identified two different PLP encephalitogenic T cell epitopes in two mouse strains. Murine PLP peptides 103-116 YKTTICGKGLSATV and 139-151 HCLGKWLGHPDKF are encephalitogenic determinants in SWR/J (H-2q) and SJL/J (H-2s) mice, respectively. The purpose of the present study was to determine the minimum sequence requirements for each of these PLP encephalitogens. In SWR/J mice, at least two distinct overlapping peptides can induce experimental autoimmune encephalomyelitis (EAE). The eleven residue sequences PLP 105-115 TTICGKGLSAT and PLP 106-116 TICGKGLSATV are encephalitogenic in SWR/J mice, but PLP 106-115 TICGKGLSAT, the decapeptide indigenous to both sequences, is non-encephalitogenic. In contrast, the shortest PLP sequence capable of inducing EAE in SJL/J mice is the nonapeptide 141-149 LGKWL-GHPD. These data indicate that encephalitogenic determinants of PLP are short contiguous peptide sequences similar in length and diversity to those of MBP.
引用
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页码:67 / 74
页数:8
相关论文
共 39 条
[1]  
Alvord E. C. J., 1984, EXPT ALLERGIC ENCEPH
[2]   PEPTIDES OF MYELIN BASIC-PROTEIN STIMULATE LYMPHOCYTES-T FROM PATIENTS WITH MULTIPLE-SCLEROSIS [J].
BAXEVANIS, CN ;
RECLOS, GJ ;
SERVIS, C ;
ANASTASOPOULOS, E ;
ARSENIS, P ;
KATSIYIANNIS, A ;
MATIKAS, N ;
LAMBRIS, JD ;
PAPAMICHAIL, M .
JOURNAL OF NEUROIMMUNOLOGY, 1989, 22 (01) :23-30
[3]   CYSTEINE-108 IS AN ACYLATION SITE IN MYELIN PROTEOLIPID PROTEIN [J].
BIZZOZERO, OA ;
GOOD, LK ;
EVANS, JE .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (01) :375-382
[4]  
BIZZOZERO OA, 1991, J BIOL CHEM, V266, P17092
[5]   INTRON-EXON SPLICE JUNCTIONS MAP AT PROTEIN SURFACES [J].
CRAIK, CS ;
SPRANG, S ;
FLETTERICK, R ;
RUTTER, WJ .
NATURE, 1982, 299 (5879) :180-182
[6]   ADOPTIVE TRANSFER OF EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS AND LOCALIZATION OF THE ENCEPHALITOGENIC EPITOPE IN THE SWR MOUSE [J].
CROSS, AH ;
HASHIM, GA ;
RAINE, CS .
JOURNAL OF NEUROIMMUNOLOGY, 1991, 31 (01) :59-66
[7]   SUSCEPTIBILITY TO PROTEOLIPID APOPROTEIN AND ITS ENCEPHALITOGENIC DETERMINANTS IN MICE [J].
ENDOH, M ;
KUNISHITA, T ;
NIHEI, J ;
NISHIZAWA, M ;
TABIRA, T .
INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1990, 92 (04) :433-438
[8]   ALLERGIC ENCEPHALOMYELITIS - STRUCTURE OF ENCEPHALITOGENIC DETERMINANT [J].
EYLAR, EH ;
HASHIM, GA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1968, 61 (02) :644-&
[9]  
EYLAR EH, 1971, J BIOL CHEM, V246, P3418
[10]   EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS - SYNTHESIS OF DISEASE-INDUCING SITE OF BASIC PROTEIN [J].
EYLAR, EH ;
CACCAM, J ;
JACKSON, JJ ;
WESTALL, FC ;
ROBINSON, AB .
SCIENCE, 1970, 168 (3936) :1220-&