Back to Authors

Tuder, Rubin M.

https://orcid.org/0000-0001-9923-607X

Mayo Clinic

University of Colorado Denver

Citations 2

Strategic Plan for Lung Vascular Research: An NHLBI-ORDR Workshop Report
Erzurum, Serpil C. , Rounds, Sharon , Stevens, Troy , Aldred, Micheala A. , Aliotta, Jason M., Asosingh, Kewal, Balaban, Robert S. , Bauer, Natalie , Bhattacharya, Jahar , Bogaard, Harm Jan , Choudhary, Gaurav , Dorn, Gerald W., Dweik, Raed A. , Fagan, Karen, Fallon, Michael B. , Finkel, Toren , Geraci, Mark W. , Gladwin, Mark T. , Humbert, Marc , Kaminski, Naftali , McMurtry, Ivan F., Newman, John H. , Nicolls, Mark R. , Rabinovitch, Marlene , Shizuru, Judy, Oka, Masahiko, Polgàr, Péter , Rodman, David M., Schumacker, Paul T. , Stenmark, Kurt R. , Tuder, Rubin M. , Voelkel, Norbert F., Sullivan, Eugene J., Weinshilboum, Richard M. , Yöder, Mervin C. , Zhao, Yingming , Gail, Dorothy B., Moore, Timothy M. , Archer, Stephen L. , Hassoun, Paul M. , Kawut, Steven M. , Loscalzo, Joseph , McDonald, Donald M. , Weinshilboum, Richard M. , Kaminski, Naftali

American Journal of Respiratory and Critical Care Medicine | September 10, 2010 | Volume: 182 | Issue: 12 | Pages: 1554-1562

10.1164/rccm.201006-0869ws Get It

Abstract The Division of Lung Diseases of the National Heart, Lung, and Blood Institute, with the Office of Rare Diseases Research, held a workshop to identify priority areas and strategic goals to enhance and accelerate research that will result in improved understanding of the lung vasculature, translational research needs, and ultimately the care of patients with pulmonary vascular diseases. Multidisciplinary experts with diverse experience in laboratory, translational, and clinical studies identified seven priority areas and discussed limitations in our current knowledge, technologies, and approaches. The focus for future research efforts include the following: (1) better characterizing vascular genotype–phenotype relationships and incorporating systems biology approaches when appropriate; (2) advancing our understanding of pulmonary vascular metabolic regulatory signaling in health and disease; (3) expanding our knowledge of the biologic relationships between the lung circulation and circulating elements, systemic vascular function, and right heart function and disease; (4) improving translational research for identifying disease-modifying therapies for the pulmonary hypertensive diseases; (5) establishing an appropriate and effective platform for advancing translational findings into clinical studies testing; and (6) developing the specific technologies and tools that will be enabling for these goals, such as question-guided imaging techniques and lung vascular investigator training programs. Recommendations from this workshop will be used within the Lung Vascular Biology and Disease Extramural Research Program for planning and strategic implementation purposes.
Resident Cellular Components of the Human Lung: Current Knowledge and Goals for Research on Cell Phenotyping and Function
Franks, Teri J. , Colby, T. V., Travis, W. D., Tuder, Rubin M. , Reynolds, Herbert Y., Brody, Arnold R., Cardoso, Wellington V. , Crystal, R G , Drake, Christopher J., Engelhardt, John F. , Frid, M., Herzog, E. , Mason, R., Phan, Sem H. , Randell, Scott H. , Rose, Mary C., Stevens, T., Serge, J., Sunday, Mary E. , Voynow, Judith A. , Weinstein, Brant M. , Whitsett, J., Williams, Mary C., Williams, Mary C.

Proceedings of the American Thoracic Society | August 28, 2008 | Volume: 5 | Issue: 7 | Pages: 763-766

10.1513/pats.200803-025hr Get It

Abstract The purpose of the workshop was to identify still obscure or novel cellular components of the lung, to determine cell function in lung development and in health that impacts on disease, and to decide promising avenues for future research to extract and phenotype these cells. Since robust technologies are now available to identify, sort, purify, culture, and phenotype cells, progress is now within sight to unravel the origins and functional capabilities of lung cells in developmental stages and in disease. The Workshop's agenda was to first discuss the lung's embryologic development, including progenitor and stem cells, and then assess the functional and structural cells in three main compartments of the lung: (1) airway cells in bronchial and bronchiolar epithelium and bronchial glands (basal, secretory, ciliated, Clara, and neuroendocrine cells); (2) alveolar unit cells (Type 1 cells, Type 2 cells, and fibroblasts in the interstitium); and (3) pulmonary vascular cells (endothelial cells from different vascular structures, smooth muscle cells, and adventitial fibroblasts). The main recommendations were to: (1) characterize with better cell markers, both surface and nonsurface, the various cells within the lung, including progenitor cells and stem cells; (2) obtain more knowledge about gene expression in specific cell types in health and disease, which will provide insights into biological and pathologic processes; (3) develop more methodologies for cell culture, isolation, sorting, co-culture, and immortalization; and (4) promote tissue banks to facilitate the procurement of tissue from normal and from diseased lung for analysis at all levels.