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Bone marrow-derived progenitor cells in end-stage lung disease patients.

Gilpin SE, Lung K, de Couto GT, Cypel M, Sato M, Singer LG, Keshavjee S, Waddell TK - BMC Pulm Med (2013)

Bottom Line: An increase in CD45⁺Collagen-1⁺ fibrocytes was found in pulmonary fibrosis and bronchiolitis obliterans patients.Plasma cytokine levels differed between disease groups, with a significant correlation between SCGF-β and CCSP⁺ cells and between Monocyte Chemotactic Protein-1 and fibrocytes.An increase in the novel CCSP⁺ epithelial-like progenitors in cystic fibrosis patients was found.

View Article: PubMed Central - HTML - PubMed

Affiliation: Latner Thoracic Surgery Research Laboratories, Division of Thoracic Surgery, Toronto General Hospital, University Health Network, University of Toronto, North Wing, 9N - 949, 200 Elizabeth Street, Toronto, ON M5G 2C4, Canada.

ABSTRACT

Background: Chronic lung diseases are marked by progressive inflammation, tissue damage and remodelling. Bone marrow-derived progenitor cells may contribute to these processes. The objectives of this study were to (1) to quantify CD45⁺Collagen-1⁺ fibrocytes and a novel epithelial-like population of bone marrow-derived cells, which express Clara Cell Secretory Protein, in patients at the time of lung transplant and (2) to evaluate mediators that may act to recruit these cells during injury.

Methods: Using an observational design, progenitor cells were quantified by flow cytometry from both bone marrow (BM) and peripheral blood (PB). Migration was tested using in vitro transwell assays. Multiplex bead-based assays were used to quantify plasma cytokines.

Results: An increase in CD45⁺Collagen-1⁺ fibrocytes was found in pulmonary fibrosis and bronchiolitis obliterans patients. Cystic fibrosis patients had an increase in CCSP⁺ cells in both the BM and PB. The proportion of CCSP⁺ cells in the BM and PB was correlated. CCSP+ cells express the chemokine receptors CCR2, CCR4, CXCR3, and CXCR4, and significantly migrated in vitro toward Stromal Derived Factor-1 (SDF-1) and Stem Cell Growth Factor-β (SCGF-β). Plasma cytokine levels differed between disease groups, with a significant correlation between SCGF-β and CCSP⁺ cells and between Monocyte Chemotactic Protein-1 and fibrocytes.

Conclusions: Different bone marrow-derived cells are found in various lung diseases. Increased fibrocytes were associated with fibrotic lung diseases. An increase in the novel CCSP⁺ epithelial-like progenitors in cystic fibrosis patients was found. These differences may be mediated by alterations in plasma cytokines responsible for cell recruitment.

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Relationship between progenitor cell populations. (A) Correlation between the percentage of Clara Cell Secretory Protein (CCSP+) Peripheral Blood Mononuclear Cells (PBMCs) and CCSP+ Bone Marrow Cells (BMCs) (n = 119 pairs). (B) Lack of correlation between the percentage of CD45+Collagen-1+ fibrocytes and CCSP+ BMCs (n = 59 pairs). (C) Lack of correlation between the percentage of CD45+Collagen-1+ fibrocytes and CCSP+ PBMC (n = 74 pairs). Spearman rank test with correlation coefficient.
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Figure 3: Relationship between progenitor cell populations. (A) Correlation between the percentage of Clara Cell Secretory Protein (CCSP+) Peripheral Blood Mononuclear Cells (PBMCs) and CCSP+ Bone Marrow Cells (BMCs) (n = 119 pairs). (B) Lack of correlation between the percentage of CD45+Collagen-1+ fibrocytes and CCSP+ BMCs (n = 59 pairs). (C) Lack of correlation between the percentage of CD45+Collagen-1+ fibrocytes and CCSP+ PBMC (n = 74 pairs). Spearman rank test with correlation coefficient.

Mentions: To investigate the relationship between CCSP+ cells within the bone marrow and the proportion in the peripheral blood, data was analyzed including all disease groups together. A significant correlation was found between the number of bone marrow and peripheral blood CCSP+ cells (Figure 3A). In contrast, no relationship was found between the number of fibrocytes and either CCSP+ BMC or PBMCs (Figure 3B-C).


Bone marrow-derived progenitor cells in end-stage lung disease patients.

Gilpin SE, Lung K, de Couto GT, Cypel M, Sato M, Singer LG, Keshavjee S, Waddell TK - BMC Pulm Med (2013)

Relationship between progenitor cell populations. (A) Correlation between the percentage of Clara Cell Secretory Protein (CCSP+) Peripheral Blood Mononuclear Cells (PBMCs) and CCSP+ Bone Marrow Cells (BMCs) (n = 119 pairs). (B) Lack of correlation between the percentage of CD45+Collagen-1+ fibrocytes and CCSP+ BMCs (n = 59 pairs). (C) Lack of correlation between the percentage of CD45+Collagen-1+ fibrocytes and CCSP+ PBMC (n = 74 pairs). Spearman rank test with correlation coefficient.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC3750607&req=5

Figure 3: Relationship between progenitor cell populations. (A) Correlation between the percentage of Clara Cell Secretory Protein (CCSP+) Peripheral Blood Mononuclear Cells (PBMCs) and CCSP+ Bone Marrow Cells (BMCs) (n = 119 pairs). (B) Lack of correlation between the percentage of CD45+Collagen-1+ fibrocytes and CCSP+ BMCs (n = 59 pairs). (C) Lack of correlation between the percentage of CD45+Collagen-1+ fibrocytes and CCSP+ PBMC (n = 74 pairs). Spearman rank test with correlation coefficient.
Mentions: To investigate the relationship between CCSP+ cells within the bone marrow and the proportion in the peripheral blood, data was analyzed including all disease groups together. A significant correlation was found between the number of bone marrow and peripheral blood CCSP+ cells (Figure 3A). In contrast, no relationship was found between the number of fibrocytes and either CCSP+ BMC or PBMCs (Figure 3B-C).

Bottom Line: An increase in CD45⁺Collagen-1⁺ fibrocytes was found in pulmonary fibrosis and bronchiolitis obliterans patients.Plasma cytokine levels differed between disease groups, with a significant correlation between SCGF-β and CCSP⁺ cells and between Monocyte Chemotactic Protein-1 and fibrocytes.An increase in the novel CCSP⁺ epithelial-like progenitors in cystic fibrosis patients was found.

View Article: PubMed Central - HTML - PubMed

Affiliation: Latner Thoracic Surgery Research Laboratories, Division of Thoracic Surgery, Toronto General Hospital, University Health Network, University of Toronto, North Wing, 9N - 949, 200 Elizabeth Street, Toronto, ON M5G 2C4, Canada.

ABSTRACT

Background: Chronic lung diseases are marked by progressive inflammation, tissue damage and remodelling. Bone marrow-derived progenitor cells may contribute to these processes. The objectives of this study were to (1) to quantify CD45⁺Collagen-1⁺ fibrocytes and a novel epithelial-like population of bone marrow-derived cells, which express Clara Cell Secretory Protein, in patients at the time of lung transplant and (2) to evaluate mediators that may act to recruit these cells during injury.

Methods: Using an observational design, progenitor cells were quantified by flow cytometry from both bone marrow (BM) and peripheral blood (PB). Migration was tested using in vitro transwell assays. Multiplex bead-based assays were used to quantify plasma cytokines.

Results: An increase in CD45⁺Collagen-1⁺ fibrocytes was found in pulmonary fibrosis and bronchiolitis obliterans patients. Cystic fibrosis patients had an increase in CCSP⁺ cells in both the BM and PB. The proportion of CCSP⁺ cells in the BM and PB was correlated. CCSP+ cells express the chemokine receptors CCR2, CCR4, CXCR3, and CXCR4, and significantly migrated in vitro toward Stromal Derived Factor-1 (SDF-1) and Stem Cell Growth Factor-β (SCGF-β). Plasma cytokine levels differed between disease groups, with a significant correlation between SCGF-β and CCSP⁺ cells and between Monocyte Chemotactic Protein-1 and fibrocytes.

Conclusions: Different bone marrow-derived cells are found in various lung diseases. Increased fibrocytes were associated with fibrotic lung diseases. An increase in the novel CCSP⁺ epithelial-like progenitors in cystic fibrosis patients was found. These differences may be mediated by alterations in plasma cytokines responsible for cell recruitment.

Show MeSH
Related in: MedlinePlus