Immunohistochemical study of tyrosine phosphorylation signaling in Hassall's corpuscles of the human thymus

被引:8
作者
Nishio, H [1 ]
Matsui, K [1 ]
Tsuji, H [1 ]
Tamura, A [1 ]
Suzuki, K [1 ]
机构
[1] Osaka Med Coll, Dept Legal Med, Takatsuki, Osaka 5698686, Japan
关键词
tyrosine phosphorylation; src family; Hassall's corpuscles; epithelial cell; thymus; stroma; immunohistochemistry;
D O I
10.1016/S0065-1281(99)80042-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tyrosine phosphorylation signaling has been reported to play a key role in thymocyte development. However, the physiological role of signaling in thymus stroma is poorly understood, and there is lack of information on the in situ localization of elements of the signaling pathway in thymus stroma. In the present study, we have found by immunohistochemical analysis that tyrosine-phosphorylated proteins are present in high amounts in Hassall's corpuscles of the thymus medulla. Hassall's corpuscles represent end stages of maturation of thymic medullary epithelium. We have also investigated the localization of the src family that is involved in tyrosine phosphorylation signaling in Hassall's corpuscles. A member of the src family protein tyrosine kinases, p59(fyn) was shown to be abundantly expressed in the outer layer of Hassall's corpuscles. Another member of the family, p60(c-src), was highly expressed in the entire Hassall's corpuscles. Furthermore, p50(csk) and p130(cas), both of which are involved in the pathway, were shown to be preferably expressed in the outer layer of Hassall's corpuscles. These findings suggest that tyrosine phosphorylation signaling may play a role in thymic medullary epithelial maturation and that the src family is involved in the process.
引用
收藏
页码:421 / 429
页数:9
相关论文
共 28 条
[1]   Cellular interactions in thymocyte development [J].
Anderson, G ;
Moore, NC ;
Owen, JJT ;
Jenkinson, EJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :73-99
[2]   INHIBITION OF T-CELL RECEPTOR BETA-CHAIN GENE REARRANGEMENT BY OVEREXPRESSION OF THE NONRECEPTOR PROTEIN TYROSINE KINASE-P56LCK [J].
ANDERSON, SJ ;
ABRAHAM, KM ;
NAKAYAMA, T ;
SINGER, A ;
PERLMUTTER, RM .
EMBO JOURNAL, 1992, 11 (13) :4877-4886
[3]   DEFECTIVE T-CELL RECEPTOR SIGNALING IN MICE LACKING THE THYMIC ISOFORM OF P59(FYN) [J].
APPLEBY, MW ;
GROSS, JA ;
COOKE, MP ;
LEVIN, SD ;
QIAN, X ;
PERLMUTTER, RM .
CELL, 1992, 70 (05) :751-763
[4]   THE THYMIC MICROENVIRONMENT [J].
BOYD, RL ;
TUCEK, CL ;
GODFREY, DI ;
IZON, DJ ;
WILSON, TJ ;
DAVIDSON, NJ ;
BEAN, AGD ;
LADYMAN, HM ;
RITTER, MA ;
HUGO, P .
IMMUNOLOGY TODAY, 1993, 14 (09) :445-459
[5]   Regulation, substrates and functions of src [J].
Brown, MT ;
Cooper, JA .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1996, 1287 (2-3) :121-149
[6]   FYN TYROSINE KINASE IS INVOLVED IN KERATINOCYTE DIFFERENTIATION CONTROL [J].
CALAUTTI, E ;
MISSERO, C ;
STEIN, PL ;
EZZELL, RM ;
DOTTO, GP .
GENES & DEVELOPMENT, 1995, 9 (18) :2279-2291
[7]  
CHENG HC, 1992, J BIOL CHEM, V267, P9248
[8]  
Cooper J.A, 1990, PEPT PROT PHOSPH, P85
[9]   NEURAL TISSUES EXPRESS HIGH-LEVELS OF THE CELLULAR SRC GENE-PRODUCT PP60C-SRC [J].
COTTON, PC ;
BRUGGE, JS .
MOLECULAR AND CELLULAR BIOLOGY, 1983, 3 (06) :1157-1162
[10]  
deWit TFR, 1996, INT IMMUNOL, V8, P1787