Docheva D, Vaerst B, Deiler S, Giunta R E, Schieker M, Volkmer E
ExperiMed, Chirurgische Klinik Innenstadt, LMU München.
Handchir Mikrochir Plast Chir. 2012 Apr;44(2):59-66. doi: 10.1055/s-0032-1309025. Epub 2012 Apr 11.
Despite its potential complications, partial aponeurectomy still is the mainstay of treatment whenever it comes to significant contracture in Dupuytren's disease. With the goal in mind to identify new therapeutic strategies we isolated and characterised cells from healthy palmar aponeurosis (Kon) and compared them to cells isolated from palmar aponeurosis of patients with a primary manifestation of Dupuytren's disease (PrimDup) as well as from patients with recurrent Dupuytren's disease (RezDup). As cells from palmar aponeurosis from patients with Dupuytren's disease share characteristics with stem cells, such as the ability to differentiate into other cell types, we analysed the stemness, morphology and integrin receptor profiles of the cells.
A total of 15 Dupuytren samples were collected from regular partial aponeurectomy procedures. From these, 3 donors without extrinsic risk factors were selected per group (RezDup, PrimDup). Cells were isolated and expanded under standard cell culture conditions. Cells from healthy patients served as control (Kon). Growth curves were produced. Cells were subjected to osteogenic and adipogenic differentiation using standard protocols. Semiquantitative PCR analysis of the integrins α2, β3, β5 and fibronectin was performed.
PrimDup cells proliferated significantly faster than control cells, which in turn proliferated faster than RezDup cells. Both PrimDup and control cells went into senescence after approximately 40 days whereas RezDup cells proliferated over the entire period of 100 days. Osteogenic and adipogenic differentiation was best in cells derived from Dupuytren patients while Kon cells differentiated poorly. PCR analysis revealed that fibronectin-binding integrins β3 and β5 are upregulated in Dupuytren's disease.
PrimDup cells grow faster than the other cell types suggesting that their growth regulation may be altered. The fact that RezDup cells do not reach senescence over 100 days in culture indicates that senescence regulating factors may be altered. As cells from Dupuytren patients differentiate better along the osteogenic and adipogenic lineages, they probably possess a higher level of stemness. Their modified integrin profile may be a key to future therapies.
尽管存在潜在并发症,但对于掌腱膜挛缩症的严重挛缩,部分腱膜切除术仍是主要的治疗方法。为了确定新的治疗策略,我们从健康掌腱膜(Kon)中分离并鉴定了细胞,并将其与从原发性掌腱膜挛缩症(PrimDup)患者以及复发性掌腱膜挛缩症(RezDup)患者的掌腱膜中分离的细胞进行了比较。由于掌腱膜挛缩症患者掌腱膜中的细胞具有干细胞的特征,如分化为其他细胞类型的能力,我们分析了这些细胞的干性、形态和整合素受体谱。
从常规部分腱膜切除术中收集了总共15份掌腱膜挛缩症样本。从这些样本中,每组(RezDup、PrimDup)选择3名无外在危险因素的供体。细胞在标准细胞培养条件下分离和扩增。健康患者的细胞用作对照(Kon)。绘制生长曲线。使用标准方案使细胞进行成骨和成脂分化。对整合素α2、β3、β5和纤连蛋白进行半定量PCR分析。
PrimDup细胞的增殖明显快于对照细胞,而对照细胞又比RezDup细胞增殖得快。PrimDup细胞和对照细胞在大约40天后进入衰老状态,而RezDup细胞在100天的整个时间段内都在增殖。掌腱膜挛缩症患者来源的细胞成骨和成脂分化最好,而Kon细胞分化较差。PCR分析显示,在掌腱膜挛缩症中,与纤连蛋白结合的整合素β3和β5上调。
PrimDup细胞比其他细胞类型生长得更快,这表明它们的生长调节可能发生了改变。RezDup细胞在培养100天内未达到衰老状态,这一事实表明衰老调节因子可能发生了改变。由于掌腱膜挛缩症患者的细胞在成骨和成脂谱系上分化更好,它们可能具有更高水平的干性。它们改变的整合素谱可能是未来治疗的关键。