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人肝内小管反应:界面多样性。

Ductular reactions in human liver: diversity at the interface.

机构信息

Department of Pathology and Medical Biology, Pathology Section, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

出版信息

Hepatology. 2011 Nov;54(5):1853-63. doi: 10.1002/hep.24613. Epub 2011 Oct 13.

Abstract

Interest in hepatic ductular reactions (DRs) has risen in recent years because of a greater appreciation of their potential roles in regeneration, fibrogenesis, and carcinogenesis. However, confusion exists because there is significant, but often unappreciated diversity at the tissue, cellular, and subcellular levels in DRs of different diseases and stages of disease. DRs are encountered in virtually all liver disorders in which there is organ-wide liver damage and cell loss, but are also present in focal lesions such as focal nodular hyperplasia and adenoma. Moreover, diverse DR phenotypes can be present within any single disease entity, and are shaped by the etiology and evolution of the disease. Although much remains to be clarified, recent studies suggest that the diversity of appearances of the DRs are likely to reflect the differing signals at the anatomic, cellular, and molecular levels driving the proliferative response. These appear to determine the relative proportions of transit-amplifying cells, the degree of hepatocytic or cholangiocytic differentiation, and their relationships with stromal, vascular, and inflammatory components. The molecular signaling pathways governing these regenerative fate decisions closely replicate those found in human and other vertebrate embryos and more generally in stem cell niches throughout the body. Like the latter, complex interactions with matrix as well as mesenchymal and inflammatory cells, vessels, and innervation are likely to be of fundamental importance. Embracing systems/tissue biological approaches to exploring DRs, in addition to more traditional cellular and molecular biological techniques, will further enhance our understanding and, thereby, we believe potentiate new therapeutic possibilities.

摘要

近年来,人们对肝小管反应 (DRs) 的兴趣日益浓厚,因为人们越来越认识到它们在再生、纤维化和癌变中的潜在作用。然而,由于不同疾病和疾病阶段的 DR 在组织、细胞和亚细胞水平上存在显著但常常未被认识到的多样性,因此存在混淆。DR 几乎存在于所有器官广泛肝损伤和细胞丢失的肝脏疾病中,但也存在于局灶性病变中,如局灶性结节性增生和腺瘤。此外,在任何单一疾病实体中都可能存在不同的 DR 表型,并且受疾病的病因和演变的影响。尽管仍有许多问题需要澄清,但最近的研究表明,DR 外观的多样性可能反映了驱动增殖反应的解剖、细胞和分子水平上不同的信号。这些信号似乎决定了过渡扩增细胞的相对比例、肝细胞或胆管细胞分化的程度,以及它们与基质、血管和炎症成分的关系。这些调控这些再生命运决定的分子信号通路与在人类和其他脊椎动物胚胎中以及更普遍地在整个身体的干细胞龛中发现的信号通路非常相似。与后者一样,与基质以及间充质和炎症细胞、血管和神经支配的复杂相互作用可能具有至关重要的意义。除了更传统的细胞和分子生物学技术外,采用系统/组织生物学方法来研究 DR 将进一步增强我们的理解,从而我们相信能够为新的治疗可能性提供潜力。

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