Volume 16, Issue 4 pp. 680-687

Impaired endothelial progenitor cell mobilization and colony-forming capacity in chronic obstructive pulmonary disease

TORU TAKAHASHI

TORU TAKAHASHI

Department of Anesthesiology, Tohoku University Hospital

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SATOSHI SUZUKI

SATOSHI SUZUKI

Division of Thoracic Surgery, Japanese Red-Cross Ishinomaki Hospital, Ishinomaki, Japan

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HIROSHI KUBO

Corresponding Author

HIROSHI KUBO

Department of Advanced Preventive Medicine for Infectious Disease, Tohoku University Graduate School of Medicine, Sendai

Hiroshi Kubo, Department of Advanced Preventive Medicine for Infectious Disease, Tohoku University Graduate School of Medicine, 2-1 Seiryoumachi, Aoba-ku, Sendai 980-8575, Japan. Email: [email protected]Search for more papers by this author
MUTSUO YAMAYA

MUTSUO YAMAYA

Department of Advanced Preventive Medicine for Infectious Disease, Tohoku University Graduate School of Medicine, Sendai

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SHIN KUROSAWA

SHIN KUROSAWA

Department of Anesthesiology, Tohoku University Hospital

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MASATO KATO

MASATO KATO

Department of Anesthesiology, Tohoku University Hospital

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First published: 01 March 2011
Citations: 20

ABSTRACT

Background and objective:  Recent studies suggest that there is endothelial impairment in both the systemic and pulmonary circulations of patients with COPD. Endothelial progenitor cells (EPC) are mobilized into the circulation by physiological stressors such as surgery, and are thought to play a role in the repair of damaged endothelium. There has been a steady increase in the frequency of surgery among COPD patients, due to the incidence of complications and lung cancer; however, the mobilization of EPC during lung resection has not been examined. We evaluated whether the mobilization and proliferation of EPC are impaired in COPD patients.

Methods:  The numbers of circulating EPC (CD34/KDR/AC133-positive mononuclear cells) were measured by flow cytometry, in COPD patients (n = 30) and non-COPD patients (n = 30) who were undergoing thoracic surgery. EPC colony-forming units (EPC-CFU) were also examined.

Results:  In non-COPD patients, both circulating EPC and EPC-CFU were significantly increased 2 h after the operation started, whereas in COPD patients there were no changes in circulating EPC or EPC-CFU, irrespective of the severity of COPD. Multiple linear regression analysis demonstrated that the presence of COPD was the only significant independent predictor of reduced mobilization of EPC during thoracic surgery.

Conclusions:  The number of circulating EPC and EPC-CFU was not increased during thoracic surgery in COPD patients. These results indicate that both the mobilization and proliferative capacity of EPC are severely impaired in COPD patients.

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