Bone marrow cells repair cigarette smoke-induced emphysema in rats

被引:107
|
作者
Huh, Jin Won [2 ]
Kim, Sun-Yong [1 ]
Lee, Ji Hyun [3 ]
Lee, Jin-Seok [1 ]
Quang Van Ta [1 ]
Kim, MiJung [4 ]
Oh, Yeon-Mok [5 ,6 ]
Lee, Yun-Song [1 ]
Lee, Sang-Do [5 ,6 ]
机构
[1] Sungkyunkwan Univ, Samsung Biomed Res Inst, Dept Mol Cell Biol, Sch Med, Suwon 440746, South Korea
[2] Inje Univ, Ilsan Paik Hosp, Dept Internal Med, Div Pulm & Crit Care Med, Goyang, South Korea
[3] CHA Univ, Coll Med, Dept Internal Med, Div Pulm & Crit Care Med, Songnam, South Korea
[4] Univ Ulsan, Asan Med Ctr, Coll Med, Dept Lab Med, Seoul, South Korea
[5] Univ Ulsan, Asan Med Ctr, Coll Med, Dept Pulm & Crit Care Med,Asthma Ctr, Seoul, South Korea
[6] Univ Ulsan, Asan Med Ctr, Coll Med, Clin Res Ctr Chron Obstruct Airway Dis, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
chronic obstructive pulmonary disease; paracrine; stem cell; smoking; MESENCHYMAL STEM-CELLS; OBSTRUCTIVE PULMONARY-DISEASE; KERATINOCYTE GROWTH-FACTOR; IMPROVES CARDIAC-FUNCTION; INDUCED ACUTE LUNG; PROGENITOR CELLS; MYOCARDIAL-INFARCTION; PARACRINE MECHANISMS; STROMAL CELLS; IN-VIVO;
D O I
10.1152/ajplung.00253.2010
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
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.
引用
收藏
页码:L255 / L266
页数:12
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