The thymus contains an extensive extracellular matrix. Although thymocytes
express integrins capable of binding to matrix molecules, the functional si
gnificance of the matrix for T cell development is uncertain. We have shown
that the matrix is associated with thymic fibroblasts which are required f
or the CD44(+) CD25(+) stage of double negative (CD4(-)8(-)) thymocyte deve
lopment. The survival of cells at this stage is dependent on IL-7 and we pr
opose that the role of fibroblasts is to present, via the matrix, IL-7 to d
eveloping T cells.