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Title: Extracellular matrix in lung development, homeostasis and disease

Here, the lung's unique extracellular matrix (ECM), while providing structural support for cells, is critical in the regulation of developmental organogenesis, homeostasis and injury-repair responses. The ECM, via biochemical or biomechanical cues, regulates diverse cell functions, fate and phenotype. The composition and function of lung ECM become markedly deranged in pathological tissue remodeling. ECM-based therapeutics and bioengineering approaches represent promising novel strategies for regeneration/repair of the lung and treatment of chronic lung diseases. In this review, we assess the current state of lung ECM biology, including fundamental advances in ECM composition, dynamics, topography, and biomechanics; the role of the ECM in normal and aberrant lung development, adult lung diseases and autoimmunity; and ECM in the regulation of the stem cell niche. We identify opportunities to advance the field of lung ECM biology and provide a set recommendations for research priorities to advance knowledge that would inform novel approaches to the pathogenesis, diagnosis, and treatment of chronic lung diseases.
Authors:
 [1] ;  [2] ; ORCiD logo [3] ; ORCiD logo [4] ;  [5] ; ORCiD logo [6] ; ORCiD logo [7] ;  [8] ;  [9] ; ORCiD logo [10] ;  [11] ;  [12] ;  [13] ;  [14] ;  [15] ; ORCiD logo [6] ; ORCiD logo [16] ;  [17] ;  [18] ; ORCiD logo [2] more »;  [19] ;  [1] « less
  1. Univ. of Alabama, Birmingham, AL (United States). Division of Pulmonary, Allergy and Critical Care Medicine
  2. Univ. of Michigan, Ann Arbor, MI (United States). Division of Pulmonary and Critical Care Medicine
  3. Univ. of Illinois, Chicago, IL (United States). Dept. of Physiology & Biophysics
  4. Univ. of Alabama, Birmingham, AL (United States). Dept. of Pediatrics
  5. Univ. of California, San Francisco, CA (United States). Lung Biology Center
  6. Yale Univ., New Haven, CT (United States). Dept. of Anesthesiology
  7. Univ. of Minnesota, Minneapolis, MN (United States). Dept. of Medicine
  8. Pacific Northwest National Lab. (PNNL), Richland, WA (United States). Systems Toxicology & Exposure Science
  9. Cornell Univ., Ithaca, NY (United States). Weill Cornell Medical College
  10. Univ. of California, San Diego, CA (United States). Sanford Consortium for Regenerative Medicine
  11. Univ. of Colorado, Denver, CO (United States). Biochemistry & Molecular Genetics
  12. Univ. of California, San Diego, CA (United States). Pediatric Respiratory Medicine
  13. Baylor College of Medicine, Houston, TX (United States). Division of Pulmonary and Critical Care
  14. National Heart, Lung, and Blood Inst., Bethesda, MD (United States). Division of Lung Diseases
  15. Johns Hopkins Univ., Baltimore, MD (United States). School of Medicine. Division of Pulmonary and Critical Care Medicine
  16. Univ. of Pittsburgh, PA (United States). Division of Environmental and Occupational Health
  17. Cedars-Sinai Medical Center, Los Angeles, CA (United States). Dept. of Medicine
  18. Mayo Clinic College of Medicine, Rochester, MN (United States). Dept. of Physiology & Biomedical Engineering
  19. Univ. of California, San Francisco, CA (United States). Division of Pulmonary and Critical Care Medicine
Publication Date:
Grant/Contract Number:
AC05-76RL01830
Type:
Accepted Manuscript
Journal Name:
Matrix Biology
Additional Journal Information:
Journal Name: Matrix Biology; Journal ID: ISSN 0945-053X
Research Org:
Pacific Northwest National Lab. (PNNL), Richland, WA (United States)
Sponsoring Org:
USDOE
Country of Publication:
United States
Language:
English
Subject:
59 BASIC BIOLOGICAL SCIENCES
OSTI Identifier:
1437148

Zhou, Yong, Horowitz, Jeffrey C., Naba, Alexandra, Ambalavanan, Namasivayam, Atabai, Kamran, Balestrini, Jenna, Bitterman, Peter B., Corley, Richard A., Ding, Bi -Sen, Engler, Adam J., Hansen, Kirk C., Hagood, James S., Kheradmand, Farrah, Lin, Qing S., Neptune, Enid, Niklason, Laura, Ortiz, Luis A., Parks, William C., Tschumperlin, Daniel J., White, Eric S., Chapman, Harold A., and Thannickal, Victor J.. Extracellular matrix in lung development, homeostasis and disease. United States: N. p., Web. doi:10.1016/j.matbio.2018.03.005.
Zhou, Yong, Horowitz, Jeffrey C., Naba, Alexandra, Ambalavanan, Namasivayam, Atabai, Kamran, Balestrini, Jenna, Bitterman, Peter B., Corley, Richard A., Ding, Bi -Sen, Engler, Adam J., Hansen, Kirk C., Hagood, James S., Kheradmand, Farrah, Lin, Qing S., Neptune, Enid, Niklason, Laura, Ortiz, Luis A., Parks, William C., Tschumperlin, Daniel J., White, Eric S., Chapman, Harold A., & Thannickal, Victor J.. Extracellular matrix in lung development, homeostasis and disease. United States. doi:10.1016/j.matbio.2018.03.005.
Zhou, Yong, Horowitz, Jeffrey C., Naba, Alexandra, Ambalavanan, Namasivayam, Atabai, Kamran, Balestrini, Jenna, Bitterman, Peter B., Corley, Richard A., Ding, Bi -Sen, Engler, Adam J., Hansen, Kirk C., Hagood, James S., Kheradmand, Farrah, Lin, Qing S., Neptune, Enid, Niklason, Laura, Ortiz, Luis A., Parks, William C., Tschumperlin, Daniel J., White, Eric S., Chapman, Harold A., and Thannickal, Victor J.. 2018. "Extracellular matrix in lung development, homeostasis and disease". United States. doi:10.1016/j.matbio.2018.03.005.
@article{osti_1437148,
title = {Extracellular matrix in lung development, homeostasis and disease},
author = {Zhou, Yong and Horowitz, Jeffrey C. and Naba, Alexandra and Ambalavanan, Namasivayam and Atabai, Kamran and Balestrini, Jenna and Bitterman, Peter B. and Corley, Richard A. and Ding, Bi -Sen and Engler, Adam J. and Hansen, Kirk C. and Hagood, James S. and Kheradmand, Farrah and Lin, Qing S. and Neptune, Enid and Niklason, Laura and Ortiz, Luis A. and Parks, William C. and Tschumperlin, Daniel J. and White, Eric S. and Chapman, Harold A. and Thannickal, Victor J.},
abstractNote = {Here, the lung's unique extracellular matrix (ECM), while providing structural support for cells, is critical in the regulation of developmental organogenesis, homeostasis and injury-repair responses. The ECM, via biochemical or biomechanical cues, regulates diverse cell functions, fate and phenotype. The composition and function of lung ECM become markedly deranged in pathological tissue remodeling. ECM-based therapeutics and bioengineering approaches represent promising novel strategies for regeneration/repair of the lung and treatment of chronic lung diseases. In this review, we assess the current state of lung ECM biology, including fundamental advances in ECM composition, dynamics, topography, and biomechanics; the role of the ECM in normal and aberrant lung development, adult lung diseases and autoimmunity; and ECM in the regulation of the stem cell niche. We identify opportunities to advance the field of lung ECM biology and provide a set recommendations for research priorities to advance knowledge that would inform novel approaches to the pathogenesis, diagnosis, and treatment of chronic lung diseases.},
doi = {10.1016/j.matbio.2018.03.005},
journal = {Matrix Biology},
number = ,
volume = ,
place = {United States},
year = {2018},
month = {3}
}