Hypoxic conditions increase hypoxia-inducible transcription factor 2alpha and enhance chondrogenesis in stem cells from the infrapatellar fat pad of osteoarthritis patients.
低酸素状態は低酸素誘導性転写因子2alphaを増加させ、変形性関節症患者の膝蓋下脂肪体由来幹細胞の軟骨形成を促進する (機械翻訳の邦題)
記録の確認項目
- 研究デザイン
- その他の原著論文
- 対象
- ヒト
- 出版年
- 2007
- 出典
- doi.org
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- 表示あり
- 出版状態
- 有効な記録
- 状態確認日
- 2026/08/17
- 収集日
- 2026/08/04
- 鮮度
- 確認期限内
- 確認段階
- 自動処理
- 記録状態
- 公開
日本語要約(機械生成)
変形性関節症患者の膝蓋下脂肪体(IPFP)由来幹細胞は関節軟骨修復の細胞源として期待される。本研究では、人工膝関節全置換術を受けた高齢患者のIPFPから接着性コロニー形成細胞を分離し、幹細胞マーカーを確認した後、軟骨形成培地で正常酸素(20%酸素)または低酸素(5%酸素)条件下で14日間凝集体培養した。その結果、低酸素条件下では細胞増殖は低下したがプロテオグリカン蓄積が増加し、DNAあたりのグリコサミノグリカン量が3.5倍に増加した。また、低酸素誘導性転写因子(HIF)2alphaの発現が増加し、HIF1alphaは変化しなかった。さらに、SOX5、SOX6、SOX9やアグリカン、バーシカン、II型、IX型、X型、XI型コラーゲンの発現も増加した。これらの結果から、低酸素環境はHIF2alphaを介してIPFP由来幹細胞の軟骨形成を促進することが示され、組織工学への応用に重要な示唆を与える。
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抄録
Stem cells derived from the infrapatellar fat pad (IPFP) are a potential source of stem cells for the repair of articular cartilage defects. Hypoxia has been shown to improve chondrogenesis in adult stem cells. In this study we investigated the effects of hypoxia on gene expression changes and chondrogenesis in stem cells from the IPFP removed from elderly patients with osteoarthritis at total knee replacement. Adherent colony-forming cells were isolated and cultured from the IPFP from total knee replacement. The cells at passage 2 were characterised for stem cell surface epitopes, and then cultured for 14 days as cell aggregates in chondrogenic medium under normoxic (20% oxygen) or hypoxic (5% oxygen) conditions. Gene expression analysis, DNA and glycosoaminoglycan assays and immunohistochemical staining were determined to assess chondrogenesis. IPFP-derived adherent colony-forming cells stained strongly for markers of adult mesenchymal stem cells, including CD44, CD90 and CD105, and they were negative for the haematopoietic cell marker CD34 and for the neural and myogenic cell marker CD56. Cell aggregates of IPFP cells showed a chondrogenic response. In hypoxic conditions there was increased matrix accumulation of proteoglycan but less cell proliferation, which resulted in 3.5-fold more glycosoaminoglycan per DNA after 14 days of culture. In hypoxia there was increased expression of hypoxia-inducible transcription factor (HIF)2alpha and not HIF1alpha, and the expression of key transcription factors SOX5, SOX6 and SOX9, and that of aggrecan, versican and collagens II, IX, X and XI, was also increased. These results show that cells with stem cell characteristics were isolated from the IPFP of elderly patients with osteoarthritis and that their response to chondrogenic culture was enhanced by lowered oxygen tension, which upregulated HIF2alpha and increased the synthesis and assembly of matrix during chondrogenesis. This has important implications for tissue engineering applications of cells derived from the IPFP.
MeSH
DOI 10.1186/ar2211
PMID 17537234
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