Abstract | AIMS: MATERIALS & METHODS: RESULTS: ASC transplantation restored pulmonary function (arterial oxygen tension and alveolar-arterial oxygen tension difference) almost to that of normal animals. Enlargement of the alveolar airspaces was inhibited. HGF and CINC-1 levels were significantly higher in the ASC group even at 2 weeks after transplantation. Sponge implantation with CINC-1 induced neovascular formation with increased HGF. In vitro secretion of HGF and CINC-1 from ASCs was promoted in the presence of IL-1β. CONCLUSION: Not only HGF, but also CINC-1, secreted from transplanted and viable ASCs presumably contributed to lung repair through angiogenesis.
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Authors | Naoki Furuya, Mitsuko Takenaga, Yuki Ohta, Yukie Tokura, Akemi Hamaguchi, Aya Sakamaki, Hirotaka Kida, Hiroshi Handa, Hiroki Nishine, Masamichi Mineshita, Teruomi Miyazawa |
Journal | Regenerative medicine
(Regen Med)
Vol. 7
Issue 4
Pg. 503-12
(Jul 2012)
ISSN: 1746-076X [Electronic] England |
PMID | 22817624
(Publication Type: Journal Article)
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Chemical References |
- Chemokine CXCL1
- Cxcl1 protein, rat
- Cytokines
- Gases
- Intercellular Signaling Peptides and Proteins
- Pancreatic Elastase
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Topics |
- Adipose Tissue
(cytology)
- Animals
- Cell- and Tissue-Based Therapy
- Cells, Cultured
- Chemokine CXCL1
(metabolism)
- Cytokines
(metabolism)
- Gases
(metabolism)
- Intercellular Signaling Peptides and Proteins
(metabolism)
- Lung
(metabolism, pathology)
- Male
- Neovascularization, Physiologic
- Pancreatic Elastase
- Prosthesis Implantation
- Pulmonary Emphysema
(chemically induced, pathology, therapy)
- Rats
- Stem Cell Transplantation
- Stem Cells
(cytology)
- Stromal Cells
(transplantation)
- Sus scrofa
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