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小鼠闭塞性气道疾病中的基因表达谱分析。

Gene expression profiling in murine obliterative airway disease.

作者信息

Lande Jeffrey D, Dalheimer Stacy L, Mueller Daniel L, Hertz Marshall I, King Richard A

机构信息

Department of Medicine, University of Minnesota Medical School, Minneapolis, USA.

出版信息

Am J Transplant. 2005 Sep;5(9):2170-84. doi: 10.1111/j.1600-6143.2005.01026.x.

Abstract

Lung and heart-lung transplantation are effective treatments for many diseases unresponsive to other therapy. However, long-term survival of recipients is limited by the development of obliterative bronchiolitis (OB). In this study, microarray analysis of a heterotopic mouse model of obliterative airway disease (OAD) was used to test the hypothesis that the expression and patterns of genes will correlate with specific changes in tracheal tissue developing a response to allotransplantation and the infiltrating cells manifesting these changes. Expression profiles observed were in accordance with the current paradigm of a predictable sequence of events, beginning with airway injury; an innate immune response followed by an adaptive immune response, including both cell-mediated and humoral components; and eventual loss of airway epithelial cells. These observations confirm and expand the list of genes and molecular processes that can be studied as potential surrogate markers or targets for intervention of OB.

摘要

肺移植和心肺联合移植是治疗许多对其他疗法无反应的疾病的有效方法。然而,闭塞性细支气管炎(OB)的发展限制了受体的长期存活。在本研究中,利用闭塞性气道疾病(OAD)异位小鼠模型进行微阵列分析,以检验基因表达和模式将与气管组织对同种异体移植产生反应的特定变化以及表现出这些变化的浸润细胞相关的假设。观察到的表达谱与当前可预测事件序列的范式一致,始于气道损伤;先天性免疫反应,随后是适应性免疫反应,包括细胞介导和体液成分;以及气道上皮细胞的最终丧失。这些观察结果证实并扩展了可作为OB潜在替代标志物或干预靶点进行研究的基因和分子过程列表。

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