Tristetraprolin Overexpression in Non-hematopoietic Cells Protects Against Acute Lung Injury in Mice.

Tristetraprolin (TTP) is a mRNA binding protein that binds to adenylate-uridylate-rich elements within the 3 ' untranslated regions of certain transcripts, such as tumor necrosis factor (Tnf) mRNA, and increases their rate of decay. Modulation of TTP expression is implicated in inflammation; however, its role in acute lung inflammation remains unknown. Accordingly, we tested the role of TTP in lipopolysaccharide (LPS)-induced acute lung injury (ALI) in mice. LPS-challenged TTP-knockout (TTPKO) mice, as well as myeloid cell-specific TTP-deficient (TTPmyeKO) mice, exhibited significant increases in lung injury, although these responses were more robust in the TTPKO. Mice with systemic overexpression of TTP (TTP Delta ARE) were protected from ALI, as indicated by significantly reduced neutrophilic infiltration, reduced levels of neutrophil chemoattractants, and histological parameters of ALI. Interestingly, while irradiated wild-type (WT) mice reconstituted with TTP(KO)hematopoietic progenitor cells (HPCs) showed exaggerated ALI, their reconstitution with the (TTPHPCs)-H-Delta ARE mitigated ALI. The reconstitution of irradiated TTP(Delta ARE)mice with HPCs from either WT or TTP(Delta ARE)donors conferred significant protection against ALI. In contrast, irradiated TTP(Delta ARE)mice reconstituted with (TTPHPCs)-H-KO had exaggerated ALI, but the response was milder as compared to WT recipients that received (TTPHPCs)-H-KO. Finally, the reconstitution of irradiated TTP(KO)recipient mice with (TTPHPCs)-H-Delta ARE did not confer any protection to the TTP(KO)mice. These data together suggest that non-HPCs-specific overexpression of TTP within the lungs protects against ALI via downregulation of neutrophil chemoattractants and reduction in neutrophilic infiltration.