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紧皮(Tsk/+)小鼠的遗传性肺气肿

Hereditary emphysema in the tight-skin (Tsk/+) mouse.

作者信息

Szapiel S V, Fulmer J D, Hunninghake G W, Elson N A, Kawanami O, Ferrans V J, Crystal R G

出版信息

Am Rev Respir Dis. 1981 Jun;123(6):680-5. doi: 10.1164/arrd.1981.123.6.680.

DOI:10.1164/arrd.1981.123.6.680
PMID:7271067
Abstract

The tight-skin (Tsk/+) mouse represents an autosomal dominant mutation characterized by increased thoracic size, large lungs, and a variety of abnormalities of loose subcutaneous connective tissue, cartilage, tendon, and bone. Because an increase in the size of the lung and thorax may result from destruction of alveolar walls and a loss of elastic recoil of the lung, the present study was undertaken to determine if the Tsk/+ mouse exhibits morphologic and physiologic characteristics of emphysema. In contrast to the lungs of normal mice, examination of the lungs of Tsk/+ mice by light and scanning electron microscopy revealed generalized enlargement of air spaces with numerous subpleural cysts and scattered bullae. In addition, many alveolar walls were either markedly thinned or broken and there was an increase in the number and size of the pores of Kohn. Consistent with these morphologic observations, the lungs of the Tsk/+ mice also exhibited physiologic characteristics consistent with emphysema. Compared to the lungs of normal mice, the lungs of Tsk/+ mice had a markedly increased total lung capacity of (1.8 +/- 0.1 ml versus 3.3 +/- 0.1 ml, p less than 0.001); compliance (0.077 +/- 0.006 ml/cm H2O versus 0.345 +/- 0.025 ml/cm H2O, p less than 0.001), and specific compliance (4.23 +/- 0.34% TLC/cm H2O versus 10.64 +/- 1.01% TLC/cm H2O, p less than 0.001). These findings suggested that the Tsk/+ mouse is a genetically determined model of emphysema that may be useful in determining the pathogenesis of destructive lung disease.

摘要

紧皮(Tsk/+)小鼠代表一种常染色体显性突变,其特征为胸廓增大、肺部肿大,以及皮下疏松结缔组织、软骨、肌腱和骨骼出现多种异常。由于肺和胸廓大小的增加可能是由于肺泡壁破坏和肺弹性回缩丧失所致,因此本研究旨在确定Tsk/+小鼠是否表现出肺气肿的形态学和生理学特征。与正常小鼠的肺相比,通过光学显微镜和扫描电子显微镜检查Tsk/+小鼠的肺,发现气腔普遍增大,有许多胸膜下囊肿和散在的肺大疱。此外,许多肺泡壁明显变薄或破裂,Kohn孔的数量和大小增加。与这些形态学观察结果一致,Tsk/+小鼠的肺也表现出与肺气肿一致的生理学特征。与正常小鼠的肺相比,Tsk/+小鼠的肺总肺容量显著增加(分别为1.8±0.1 ml和3.3±0.1 ml,p<0.001);顺应性(分别为0.077±0.006 ml/cm H2O和0.345±0.025 ml/cm H2O,p<0.001),以及比顺应性(分别为4.23±0.34% TLC/cm H2O和10.64±1.01% TLC/cm H2O,p<0.001)。这些发现表明,Tsk/+小鼠是一种由基因决定的肺气肿模型,可能有助于确定破坏性肺病的发病机制。

相似文献

1
Hereditary emphysema in the tight-skin (Tsk/+) mouse.紧皮(Tsk/+)小鼠的遗传性肺气肿
Am Rev Respir Dis. 1981 Jun;123(6):680-5. doi: 10.1164/arrd.1981.123.6.680.
2
A scanning electron microscopic investigation of genetic emphysema in tight-skin, pallid, and beige mice, three different C57 BL/6J mutants.对三种不同的C57 BL/6J突变体——紧皮小鼠、苍白小鼠和米色小鼠的遗传性肺气肿进行的扫描电子显微镜研究。
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Hereditary emphysema in the tight-skin mouse. Evaluation of pathogenesis.紧皮小鼠的遗传性肺气肿。发病机制评估。
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Electron microscopic observations of elastic fibres in the lung and aorta of tight-skin and beta-aminopropionitrile-fed mice.
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Emphysema-like changes in the lungs of the blotchy mouse.斑点小鼠肺部的肺气肿样改变。
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Breakdown of lung framework and an increase in pores of Kohn as initial events of emphysema and a cause of reduction in diffusing capacity.肺结构破坏以及科恩孔增加是肺气肿的初始事件,也是弥散能力降低的原因。
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Mild emphysema is associated with reduced elastic recoil and increased lung size but not with air-flow limitation.轻度肺气肿与弹性回缩力降低和肺容积增加有关,但与气流受限无关。
Am Rev Respir Dis. 1987 Oct;136(4):867-71. doi: 10.1164/ajrccm/136.4.867.

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