Phospholipase D isoforms differentially regulate leukocyte responses to acute lung injury
| Autor: | Rebecca M. Baron, Taylor E. Miller, David N. Douda, Julian Gomez-Cambronero, Alexander H. Tavares, Bruce D. Levy, Judie A. Howrylak, Raja-Elie E. Abdulnour, Karen M. Henkels, Laura E. Fredenburgh |
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| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
Gene isoform Male ARDS Neutrophils Phagocytosis Immunology Acute Lung Injury Biology Lung injury Article 03 medical and health sciences Mice Gene expression medicine Leukocytes Phospholipase D Immunology and Allergy Animals Humans Protein Isoforms Lung Cells Cultured Mice Knockout Gene knockdown Respiratory Distress Syndrome PLD2 Macrophages Cell Biology medicine.disease Mice Inbred C57BL 030104 developmental biology Case-Control Studies Cancer research Female |
| Zdroj: | Journal of leukocyte biology. 103(5) |
| ISSN: | 1938-3673 |
| Popis: | Phospholipase D (PLD) plays important roles in cellular responses to tissue injury that are critical to acute inflammatory diseases, such as the acute respiratory distress syndrome (ARDS). We investigated the expression of PLD isoforms and related phospholipid phosphatases in patients with ARDS, and their roles in a murine model of self-limited acute lung injury (ALI). Gene expression microarray analysis on whole blood obtained from patients that met clinical criteria for ARDS and clinically matched controls (non-ARDS) demonstrated that PLD1 gene expression was increased in patients with ARDS relative to non-ARDS and correlated with survival. In contrast, PLD2 expression was associated with mortality. In a murine model of self-resolving ALI, lung Pld1 expression increased and Pld2 expression decreased 24 h after intrabronchial acid. Total lung PLD activity was increased 24 h after injury. Pld1−/− mice demonstrated impaired alveolar barrier function and increased tissue injury relative to WT and Pld2−/−, whereas Pld2−/− mice demonstrated increased recruitment of neutrophils and macrophages, and decreased tissue injury. Isoform-specific PLD inhibitors mirrored the results with isoform-specific Pld-KO mice. PLD1 gene expression knockdown in human leukocytes was associated with decreased phagocytosis by neutrophils, whereas reactive oxygen species production and phagocytosis decreased in M2-macrophages. PLD2 gene expression knockdown increased neutrophil and M2-macrophage transmigration, and increased M2-macrophage phagocytosis. These results uncovered selective regulation of PLD isoforms after ALI, and opposing effects of selective isoform knockdown on host responses and tissue injury. These findings support therapeutic strategies targeting specific PLD isoforms for the treatment of ARDS. |
| Databáze: | OpenAIRE |
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