Our data demonstrate that increased intracellular expression of thymosin 4 (T4) is necessary and sufficient to induce plasminogen activator inhibitor type 1 (PAI-1) gene expression in endothelial cells. To describe the mechanism of this effect, we produced T4 mutants with impaired functional motifs and tested their intracellular location and activity. Cytoplasmic distributions of T4 (AcSDKPT/4A) , T4 (KLKKTET/7A) , and T4 (K16A) mutants fused with green fluorescent protein did not differ significantly from those of wild-type T4. Overexpression of T4, T4 (AcSDKPT/4A) , and T4 (K16A) affected intracellular formation of actin filaments. As expected, T4 (K16A) uptake by nuclei was impaired. On the other hand, overexpression of T4 (KLKKTET/7A) resulted in developing the actin filament network typical of adhering cells, indicating that the mutant lacked the actin binding site. The mechanism by which intracellular T4 induced the PAI-1 gene did not depend upon the N-terminal tetrapeptide AcSDKP and depended only partially on its ability to bind G-actin or enter the nucleus. Both T4 and T4 (AcSDKPT/4A) induced the PAI-1 gene to the same extent, whereas mutants T4 (KLKKTET/7A) and T4 (K16A) retained about 60% of the original activity. By proteomic analysis, the Ku80 subunit of ATPdependent DNA helicase II was found to be associated with T4. Ku80 and T4 consistently co-immunoprecipitated in a complex from endothelial cells. Co-transfection of endothelial cells with the Ku80 deletion mutants and T4 showed that the C-terminal arm domain of Ku80 is directly involved in this interaction. Furthermore, down-regulation of Ku80 by specific short interference RNA resulted in dramatic reduction in PAI-1 expression at the level of both mRNA and protein synthesis. These data suggest that Ku80 functions as a novel receptor for T4 and mediates its intracellular activity.2 is the most abundant member of the highly conserved family of acidic polypeptides called -thymosins. Although it is a typical intracellular polypeptide, it plays numerous roles, both intracellularly and extracellularly. Numerous observations indicate that T4 is involved in adhesion and spreading of fibroblasts (1, 2), differentiation of endothelial cells (3, 4), directional migration of endothelial cells and keratinocytes (5-8), angiogenesis (3-6, 9, 10), wound healing (6, 7, 11), hair follicle growth (8), and apoptosis (12, 13), and has been described to possess anti-inflammatory properties (11,14). In addition, elevated T4 expression has been observed in various malignant cell lines and tumors (15-17) and its levels seem to be associated with increased tumorigenicity and metastatic potential (10, 13, 18 -20). The increased expression of T4 correlates with the invasive capability of the cells, the degree of morphologic transformation, and disintegration of actin filaments (21). Recent studies have also correlated increased T4 expression with potentiated cell growth (13, 22) but this observation seems not to be universal (2, 10).T4 is conside...