Liposome-mediated gene transfer to lung isografts
| Autor: | William O. Osburn, Wei Zhang, Bassem N. Mora, David Peterson, G. Alexander Patterson, Teng C. Lee, Joel D. Cooper, Ronald K. Scheule, Jennifer B. Nietupski, Carlos H.R. Boasquevisque, M D Botney, Matthew Bernstein |
|---|---|
| Rok vydání: | 1997 |
| Předmět: |
Chloramphenicol O-Acetyltransferase
Male Pulmonary and Respiratory Medicine Pathology medicine.medical_specialty DNA Complementary Time Factors In situ hybridization Kidney Transfection Andrology In vivo Genes Reporter medicine Animals Lung business.industry Myocardium Genetic transfer Rats Inbred F344 Rats Transplantation Transplantation Isogeneic medicine.anatomical_structure Liver Liposomes Feasibility Studies Tumor necrosis factor alpha Surgery business Cardiology and Cardiovascular Medicine Ex vivo Lung Transplantation |
| Zdroj: | The Journal of Thoracic and Cardiovascular Surgery. 114(5):783-792 |
| ISSN: | 0022-5223 |
| DOI: | 10.1016/s0022-5223(97)70082-5 |
| Popis: | Objectives: Our objectives were to determine the feasibility, efficacy, and safety of in vivo and ex vivo liposome-mediated gene transfer to lung isografts. Methods: Fischer rats were divided into three main groups: (1) Nontransplant setting: Liposome–chloramphenicol acetyl transferase cDNA was intravenously injected, and lungs were harvested at different time points: 2, 6, 12, and 24 hours; 2, 5, 8, and 21 days ( n = 3). Chloramphenicol acetyl transferase activity was determined in lungs, hearts, livers, and kidneys. The distribution and type of transfected cells were evaluated by in situ hybridization. Lung toxicity was assessed by arterial oxygen tension, histology, and tumor necrosis factor–α levels. (2) In vivo graft transfection: Left lungs were transplanted 6 hours, 4 hours, and 15 minutes after intravenous injection and were assessed for chloramphenicol acetyl transferase activity and arterial oxygen tension on postoperative day 2. (3) Ex vivo graft transfection: Grafts were infused ex vivo with either 660 μg ( n = 3) or 330 μg ( n = 3) of DNA complexed to liposomes and stored at 10° C for 4 hours. Chloramphenicol acetyl transferase activity was assessed 44 hours after transplantation. Results: Transgene expression was detected in endothelial cells, macrophages, and interstitial cells. Chloramphenicol acetyl transferase activity was present as early as 2 hours, increased significantly between 6 hours and 8 days, and then decreased to minimal levels by 21 days. Chloramphenicol acetyl transferase activity was greatest in donor lungs and hearts and minimal in livers and kidneys. Arterial oxygen tension was normal in treated animals. Inflammation was minimal, and tumor necrosis factor–α levels increased only sevenfold in treated animals. Conclusion: In vivo and ex vivo liposome-mediated gene transfer to lung isografts allows significant transgene expression with minimal effects on graft function. (J Thorac Cardiovasc Surg 1997;114:783-92) |
| Databáze: | OpenAIRE |
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