4.5 Article

Bone marrow cells repair cigarette smoke-induced emphysema in rats

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajplung.00253.2010

Keywords

chronic obstructive pulmonary disease; paracrine; stem cell; smoking

Funding

  1. National Research Foundation (NRF) of Korea [KRF-2008-E00116, E00226, 2008-E00102]
  2. Ministry of Health and Welfare [A040153]
  3. Asan Institute for Life Science [06-381]
  4. Korea Healthcare Technology R&D Welfare & Family Affairs Project [A084753]
  5. Korea Health Promotion Institute [A084753] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. National Research Foundation of Korea [2008-314-E00102] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

Ask authors/readers for more resources

Huh JW, Kim S-Y, Lee JH, Lee J-S, Van Ta Q, Kim M, Oh Y-M, Lee Y-S, Lee S-D. Bone marrow cells repair cigarette smoke-induced emphysema in rats. Am J Physiol Lung Cell Mol Physiol 301: L255-L266, 2011. First published May 27, 2011; doi:10.1152/ajplung.00253.2010.-The therapeutic potential of stem cells in chronic obstructive pulmonary disease is not well known although stem cell therapy is effective in models of other pulmonary diseases. We tested the capacities of bone marrow cells (BMCs), mesenchymal stem cells (MSCs), and conditioned media of MSCs (MSC-CM) to repair cigarette smoke-induced emphysema. Inbred female Lewis rats were exposed to cigarette smoke for 6 mo and then received BMCs, MSCs, or MSC-CM from male Lewis rats. For 2 mo after injection, the BMC treatment gradually alleviated the cigarette smoke-induced emphysema and restored the increased mean linear intercept. The BMC treatment significantly increased cell proliferation and the number of small pulmonary vessels, reduced apoptotic cell death, attenuated the mean pulmonary arterial pressure, and inhibited muscularization in small pulmonary vessels. However, only a few male donor cells were detected from 1 day to 1 mo after BMC administration. The MSCs and cell-free MSC-CM also induced the repair of emphysema and increased the number of small pulmonary vessels. Our data show that BMC, MSCs, and MSC-CM treatment repaired cigarette smoke-induced emphysema. The repair activity of these treatments is consistent with a paracrine effect rather than stem cell engraftment because most of the donor cells disappeared and because cell-free MSC-CM also induced the repair.

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