Integrating mechanisms of pulmonary fibrosis.

Integrating mechanisms of pulmonary fibrosis.
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DOI:
10.1084/jem.20110551
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发表时间:
2011-07-04
期刊:
The Journal of experimental medicine
影响因子:
--
通讯作者:
Wynn TA
Wynn TA
中科院分区:
其他
文献类型:
--
作者:
Wynn TA

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肺纤维化是一种复杂且异质性的疾病;对影响其发病机制的细胞和分子机制进行更详细和综合的了解将有助于新疗法的设计。肺纤维化是一种高度异质性和致命的病理过程,治疗选择有限。尽管对肺纤维化发病机制的研究经常集中在调节胶原蛋白分泌肌成纤维细胞的增殖、活化和分化的机制上,但最近的研究已经确定了在各种情况下与纤维化的起始和进展密切相关的新的致病机制。对肺纤维化的细胞和分子机制进行更详细和综合的了解可能有助于为这种破坏性和复杂疾病的有效治疗铺平道路。
Pulmonary fibrosis is a complex and heterogeneous disease; a more detailed and integrated understanding of the cellular and molecular mechanisms influencing its pathogenesis will aid the design of new therapies. Pulmonary fibrosis is a highly heterogeneous and lethal pathological process with limited therapeutic options. Although research on the pathogenesis of pulmonary fibrosis has frequently focused on the mechanisms that regulate the proliferation, activation, and differentiation of collagen-secreting myofibroblasts, recent studies have identified new pathogenic mechanisms that are critically involved in the initiation and progression of fibrosis in a variety of settings. A more detailed and integrated understanding of the cellular and molecular mechanisms of pulmonary fibrosis could help pave the way for effective therapeutics for this devastating and complex disease.
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