Phagocytic cells of the thymic reticulum interact with thymocytes via extracellular matrix ligands and receptors

被引:12
作者
Ayres-Martins, S
Lannes-Vieira, J
Farias-de-Oliveira, DA
Brito, JM
Villa-Verde, DMS
Savino, W
机构
[1] Inst Oswaldo Cruz, Oswaldo Cruz Fdn, Dept Immunol, Lab Thymus Res, BR-21045900 Rio De Janeiro, Brazil
[2] Inst Oswaldo Cruz, Oswaldo Cruz Fdn, Dept Immunol, Lab Autoimmun & Immunoregulat, Rio De Janeiro, Brazil
[3] Fed Univ Alagoas, Dept Pathol, Maceio, Brazil
[4] Fed Univ Rio De Janeiro, Lab Cell Proliferat & Differentat, Dept Histol & Embryol, Inst Biomed Sci, Rio De Janeiro, Brazil
关键词
thymic microenvironment; thymic phagocytic cells; thymic epithelial cells; thymocytes; fibronectin; laminin; integrins; cell adhesion;
D O I
10.1016/j.cellimm.2004.06.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We previously showed that, in the context of thymic epithelial cells, thymocyte migration is partially controlled by extracellular matrix (ECM)-mediated interactions. Herein we evaluated whether these interactions could be involved in cell migration related events in the context of non-epithelial cells of the thymic microenvironment, the phagocytic cells of the thymic reticulum (PTR). We first showed, by immunocytochemistry, cytofluorometry, and RT-PCR, that PTR produce ECM components, including fibronectin and laminin, and express the corresponding integrin-type receptors, VLA-4, VLA-5, and VLA-6. Thyrnocytes adhere onto PTR monolayers, with immature CD4(+)CD8(+) cells being predominant. Importantly, such an adhesion is partially mediated by ECM ligands and receptors, since it was impaired by anti-ECM or anti-ECM receptor antibodies. Conjointly, our data reveal that the ECM-dependence for thymocyte adhesion onto the thymic microenvironment is not restricted to the epithelia] cells, being also seen when they encounter non-epithelial phagocytic cells. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:21 / 30
页数:10
相关论文
共 33 条
[21]   EXTRACELLULAR-MATRIX PROTEINS IN INTRATHYMIC T-CELL MIGRATION AND DIFFERENTIATION [J].
SAVINO, W ;
VILLAVERDE, DMS ;
LANNESVIEIRA, J .
IMMUNOLOGY TODAY, 1993, 14 (04) :158-161
[22]   Intrathymic T-cell migration: a combinatorial interplay of extracellular matrix and chemokines? [J].
Savino, W ;
Mendes-da-Cruz, DA ;
Silva, JS ;
Dardenne, M ;
Cotta-de-Almeida, V .
TRENDS IN IMMUNOLOGY, 2002, 23 (06) :305-313
[23]  
SAVINO W, 1986, THYMUS, V8, P245
[24]   The conveyor belt model for intrathymic T-cell migration [J].
Savino, W ;
Dardenne, M ;
Carnaud, C .
IMMUNOLOGY TODAY, 1996, 17 (02) :97-98
[25]   Neuroendocrine control of thymus physiology [J].
Savino, W ;
Dardenne, M .
ENDOCRINE REVIEWS, 2000, 21 (04) :412-443
[26]  
SAVINO W, 2000, DEV IMMUNOL, V7, P1
[27]  
SAWADA M, 1992, J IMMUNOL, V149, P3517
[28]   THYMIC EMIGRATION - CONVEYOR BELTS OR LUCKY DIPS [J].
SCOLLAY, R ;
GODFREY, DI .
IMMUNOLOGY TODAY, 1995, 16 (06) :268-273
[29]  
VANEWIJK W, 1988, LAB INVEST, V59, P579
[30]   EXTRACELLULAR-MATRIX COMPONENTS OF THE MOUSE THYMUS MICROENVIRONMENT .4. MODULATION OF THYMIC NURSE CELLS BY EXTRACELLULAR-MATRIX LIGANDS AND RECEPTORS [J].
VILLAVERDE, DMS ;
LAGROTACANDIDO, JM ;
VANNIERSANTOS, MA ;
CHAMMAS, R ;
BRENTANI, RR ;
SAVINO, W .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (03) :659-664