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胶原 19 突变诱导的食管平滑肌异常。

Abnormalities in esophageal smooth muscle induced by mutations in collagen XIX.

机构信息

Department of Matrix Medicine, Faculty of Medicine, Oita University, Yufu, Oita, 879-5593, Japan.

Division of Life Science Research, Research Promotion Institute, Oita University, Yufu, Oita, 879-5593, Japan.

出版信息

Histochem Cell Biol. 2022 Feb;157(2):205-216. doi: 10.1007/s00418-021-02059-9. Epub 2022 Jan 7.

DOI:10.1007/s00418-021-02059-9
PMID:34993640
Abstract

Collagen XIX is a nonfibrillar collagen that localizes in restricted tissues at very low amounts. A previous study on Col19a1 null mice revealed that collagen XIX is involved in esophageal muscle physiology and morphogenesis. Here, we use histological analysis to show that mice with a Col19a1 mutant lacking the NC3 domain and seven collagen triplets display abnormal transition of smooth to striated muscle in the abdominal segment of esophagus, and a widened esophagus with age. With two newly prepared antibodies, we analyzed the expression of collagen XIX in the mouse esophagus and show that collagen XIX colocalizes with α-smooth muscle actin. By immunoelectron microscopy, we confirmed the localization of collagen XIX in esophageal smooth muscle cells. Col19a1 mutant mice contained reduced levels of mutated Col19a1 mRNA. Interestingly, hepatocyte growth factor, which has an important role in esophageal striated muscle development, was reduced in the esophagus of the Col19a1 mutant mice. These findings suggest that collagen XIX may be critical for the function of esophageal smooth muscle cells as a scaffold for anteroposterior migration of esophagus-striated muscle cells.

摘要

胶原 19 是一种非纤维胶原,在含量非常低的特定组织中定位。之前对 Col19a1 基因敲除小鼠的研究表明,胶原 19 参与食管肌肉生理学和形态发生。在这里,我们使用组织学分析表明,缺乏 NC3 结构域和七个胶原三螺旋的 Col19a1 突变小鼠显示出食管腹段平滑肌到横纹肌的异常过渡,并且随着年龄的增长食管变宽。使用两种新制备的抗体,我们分析了小鼠食管中胶原 19 的表达,并表明胶原 19 与α-平滑肌肌动蛋白共定位。通过免疫电子显微镜,我们证实了胶原 19 在食管平滑肌细胞中的定位。Col19a1 突变小鼠中突变的 Col19a1 mRNA 水平降低。有趣的是,在 Col19a1 突变小鼠的食管中,对食管横纹肌发育具有重要作用的肝细胞生长因子减少。这些发现表明,胶原 19 可能是食管平滑肌细胞功能的关键,作为食管横纹肌细胞前后迁移的支架。

相似文献

1
Abnormalities in esophageal smooth muscle induced by mutations in collagen XIX.胶原 19 突变诱导的食管平滑肌异常。
Histochem Cell Biol. 2022 Feb;157(2):205-216. doi: 10.1007/s00418-021-02059-9. Epub 2022 Jan 7.
2
Collagen type XIX regulates cardiac extracellular matrix structure and ventricular function.胶原 19 型调节心脏细胞外基质结构和心室功能。
Matrix Biol. 2022 May;109:49-69. doi: 10.1016/j.matbio.2022.03.007. Epub 2022 Mar 26.
3
Esophageal muscle physiology and morphogenesis require assembly of a collagen XIX-rich basement membrane zone.食管肌肉生理学和形态发生需要富含ⅩⅨ型胶原蛋白的基底膜区的组装。
J Cell Biol. 2004 Aug 16;166(4):591-600. doi: 10.1083/jcb.200402054. Epub 2004 Aug 9.
4
Collagen XIX is expressed by interneurons and contributes to the formation of hippocampal synapses.胶原蛋白 XIX 由中间神经元表达,并有助于海马突触的形成。
J Comp Neurol. 2010 Jan 10;518(2):229-53. doi: 10.1002/cne.22228.
5
Ubiquitous expression of the alpha1(XIX) collagen gene (Col19a1) during mouse embryogenesis becomes restricted to a few tissues in the adult organism.α1(XIX)胶原基因(Col19a1)在小鼠胚胎发育过程中的广泛表达,在成年生物体中局限于少数组织。
J Biol Chem. 1997 Jul 4;272(27):17104-11. doi: 10.1074/jbc.272.27.17104.
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Structure of the human type XIX collagen (COL19A1) gene, which suggests it has arisen from an ancestor gene of the FACIT family.人类第十九型胶原蛋白(COL19A1)基因的结构,这表明它起源于FACIT家族的一个祖先基因。
Genomics. 1997 Oct 15;45(2):304-12. doi: 10.1006/geno.1997.4921.
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Embryonic expression of type XIX collagen is transient and confined to muscle cells.XIX型胶原蛋白的胚胎表达是短暂的,且局限于肌肉细胞。
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Ultrastructural analysis of the smooth-to-striated transition zone in the developing mouse esophagus: emphasis on apoptosis of smooth and origin and differentiation of striated muscle cells.发育中小鼠食管平滑肌向横纹肌过渡区的超微结构分析:着重于平滑肌细胞凋亡及横纹肌细胞的起源与分化
Dev Dyn. 2005 Jul;233(3):964-82. doi: 10.1002/dvdy.20436.
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Type XIX collagen: a promising biomarker from the basement membranes.XIX型胶原蛋白:一种来自基底膜的有前景的生物标志物。
Neural Regen Res. 2020 Jun;15(6):988-995. doi: 10.4103/1673-5374.270299.
10
A neo-esophagus reconstructed by cultured human esophageal epithelial cells, smooth muscle cells, fibroblasts, and collagen.
ASAIO J. 2004 May-Jun;50(3):261-6. doi: 10.1097/01.mat.0000123688.45717.a4.

本文引用的文献

1
A distinct cardiopharyngeal mesoderm genetic hierarchy establishes antero-posterior patterning of esophagus striated muscle.明确的心咽中胚层遗传层次结构建立了食管横纹肌的前-后模式。
Elife. 2019 Sep 19;8:e47460. doi: 10.7554/eLife.47460.
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Selective measurement of α smooth muscle actin: why β-actin can not be used as a housekeeping gene when tissue fibrosis occurs.α平滑肌肌动蛋白的选择性检测:组织纤维化发生时β-肌动蛋白为何不能用作内参基因。
BMC Mol Biol. 2017 Apr 27;18(1):12. doi: 10.1186/s12867-017-0089-9.
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Type XIX collagen: A new partner in the interactions between tumor cells and their microenvironment.
XIX型胶原蛋白:肿瘤细胞与其微环境相互作用中的新伙伴。
Matrix Biol. 2017 Jan;57-58:169-177. doi: 10.1016/j.matbio.2016.07.010. Epub 2016 Aug 1.
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A simple solution for antibody signal enhancement in immunofluorescence and triple immunogold assays.免疫荧光和三重免疫金测定中抗体信号增强的简单解决方案。
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Collagen-derived matricryptins promote inhibitory nerve terminal formation in the developing neocortex.胶原蛋白衍生的基质隐窝蛋白促进发育中的新皮质中抑制性神经末梢的形成。
J Cell Biol. 2016 Mar 14;212(6):721-36. doi: 10.1083/jcb.201509085.
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A Cranial Mesoderm Origin for Esophagus Striated Muscles.颅中胚层起源于食管横纹肌。
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BMP signaling in the development of the mouse esophagus and forestomach.BMP 信号在小鼠食管和前胃发育中的作用。
Development. 2010 Dec;137(24):4171-6. doi: 10.1242/dev.056077. Epub 2010 Nov 10.
8
Collagen XIX is expressed by interneurons and contributes to the formation of hippocampal synapses.胶原蛋白 XIX 由中间神经元表达,并有助于海马突触的形成。
J Comp Neurol. 2010 Jan 10;518(2):229-53. doi: 10.1002/cne.22228.
9
Deletion of Pax7 changes the tunica muscularis of the mouse esophagus from an entirely striated into a mixed phenotype.Pax7基因的缺失使小鼠食管的肌层从完全的横纹肌转变为混合表型。
Dev Dyn. 2009 Apr;238(4):864-74. doi: 10.1002/dvdy.21898.
10
Trimerization and triple helix stabilization of the collagen XIX NC2 domain.胶原蛋白XIX NC2结构域的三聚化和三螺旋稳定化
J Biol Chem. 2008 Dec 5;283(49):34345-51. doi: 10.1074/jbc.M806352200. Epub 2008 Oct 8.