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[慢性阻塞性肺疾病患者肋间肌卫星细胞的激活]

[Activation of satellite cells in the intercostal muscles of patients with chronic obstructive pulmonary disease].

作者信息

Martínez-Llorens Juana, Casadevall Carme, Lloreta Josep, Orozco-Levi Mauricio, Barreiro Esther, Broquetas Joan, Gea Joaquim

机构信息

Servei de Pneumologia, Hospital del Mar-IMIM, Barcelona, España.

出版信息

Arch Bronconeumol. 2008 May;44(5):239-44.

Abstract

OBJECTIVE

The respiratory muscles of patients with chronic obstructive pulmonary disease (COPD) display evidence of structural damage in parallel with signs of adaptation. We hypothesized that this can only be explained by the simultaneous activation of satellite cells. The aim of this study was to analyze the number and activation of those cells along with the expression of markers of microstructural damage that are frequently associated with regeneration.

PATIENTS AND METHODS

The study included 8 patients with severe COPD (mean [SD] forced expiratory volume in 1 second, 33% [9%] of predicted) and 7 control subjects in whom biopsies were performed of the external intercostal muscle. The samples were analyzed by light microscopy to assess muscle fiber phenotype, electron microscopy to identify satellite cells, and real-time polymerase chain reaction to analyze the expression of the following markers: insulin-like growth factor 1, mechano growth factor, and embryonic and perinatal myosin heavy chains (MHC) as markers of microstructural damage; Pax-7 and m-cadherin as markers of the presence and activation of satellite cells, respectively; and MHC-I, IIa, and IIx as determinants of muscle fiber phenotype.

RESULTS

The patients had larger fibers than healthy subjects (54 [6] vs 42 [4] microm(2); P< .01) with a similar or slightly increased proportion of satellite cells, as measured by ultrastructural analysis (4.3% [1%] vs 3.7% [3.5%]; P>.05) or expression of Pax-7 (5.5 [4.1] vs 1.6 [0.8] arbitrary units [AU]; P< .05). In addition, there was greater activation of satellite cells in the patients, as indicated by increased expression of m-cadherin (3.8 [2.1] vs 1.0 [1.2] AU; P=.05). This was associated with increased expression of markers of microstructural damage: insulin-like growth factor 1, 0.35 (0.34) vs 0.09 (0.08) AU (P< .05); mechano growth factor, 0.45 (0.55) vs 0.13 (0.17) AU (P=.05).

CONCLUSIONS

The intercostal muscles of patients with severe COPD show indirect signs of microstructural damage accompanied by satellite cell activation. This suggests the presence of ongoing cycles of lesion and repair that could partially explain the maintenance of the structural properties of the muscle.

摘要

目的

慢性阻塞性肺疾病(COPD)患者的呼吸肌表现出结构损伤的证据,同时伴有适应性迹象。我们推测,这只能通过卫星细胞的同时激活来解释。本研究的目的是分析这些细胞的数量和激活情况,以及与再生相关的微观结构损伤标志物的表达。

患者和方法

该研究纳入了8例重度COPD患者(一秒用力呼气容积平均[标准差]为预测值的33%[9%])和7名对照受试者,对其肋间外肌进行活检。通过光学显微镜分析样本以评估肌纤维表型,通过电子显微镜鉴定卫星细胞,并通过实时聚合酶链反应分析以下标志物的表达:胰岛素样生长因子1、机械生长因子以及胚胎和围产期肌球蛋白重链(MHC)作为微观结构损伤的标志物;Pax-7和m-钙黏蛋白分别作为卫星细胞存在和激活的标志物;以及MHC-I、IIa和IIx作为肌纤维表型的决定因素。

结果

与健康受试者相比,患者的肌纤维更大(54[6]对42[4]μm²;P<.01),通过超微结构分析测量,卫星细胞比例相似或略有增加(4.3%[1%]对3.7%[3.5%];P>.05),或Pax-7表达情况(5.5[4.1]对1.6[0.8]任意单位[AU];P<.05)。此外,患者的卫星细胞激活程度更高,m-钙黏蛋白表达增加表明了这一点(3.8[2.1]对1.0[1.2]AU;P=.05)。这与微观结构损伤标志物的表达增加相关:胰岛素样生长因子1,0.35(0.34)对0.09(0.08)AU(P<.05);机械生长因子,0.45(0.55)对0.13(0.17)AU(P=.05)。

结论

重度COPD患者的肋间肌显示出微观结构损伤的间接迹象,并伴有卫星细胞激活。这表明存在持续的损伤和修复循环,这可能部分解释了肌肉结构特性的维持。

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