Suppr超能文献

Dp71、肌养蛋白和β-肌营养不良蛋白聚糖在PC12/L6细胞共培养物中的表达与分布

Dp71, utrophin and beta-dystroglycan expression and distribution in PC12/L6 cell cocultures.

作者信息

Ilarraza-Lomeli Ramses, Cisneros-Vega Bulmaro, Cervantes-Gomez Maria de Lourdes, Mornet Dominique, Montañez Cecilia

机构信息

Department of Genetics and Molecular Biology, Centre for Research and Advanced Studies (CINVESTAV-IPN), San Pedro Zacatenco, Mexico City, Mexico.

出版信息

Neuroreport. 2007 Oct 29;18(16):1657-61. doi: 10.1097/WNR.0b013e3282f0e42d.

Abstract

Function of dystrophin Dp71 isoforms is unknown but seems related to neurite outgrowth and synapse formation. To evaluate Dp71 role in myoneural synapses, we established a coculture model using PC12 cells and L6 myotubes and analyzed expression and localization of Dp71 and related proteins, utrophin and beta-dystroglycan, in PC12 cells. Confocal microscopy showed Dp71d isoform in PC12 nuclei, golgi-complex-like and endoplasmic reticulum-like structures, whereas Dp71ab concentrates at neurite tips and cytoplasm, colocalizing with beta-dystroglycan, utrophin, synaptophysin and acetylcholine receptors. Evidences suggest that Dp71ab isoform, unlike Dp71d, may take part in neurite-related processes. This is the first work on Dp and members of Dp-associated protein complex roles in a cell-line based coculturing system, which may be useful in determining Dp71 isoforms associations.

摘要

肌营养不良蛋白Dp71亚型的功能尚不清楚,但似乎与神经突生长和突触形成有关。为了评估Dp71在肌神经突触中的作用,我们建立了一个使用PC12细胞和L6肌管的共培养模型,并分析了PC12细胞中Dp71及相关蛋白、抗肌萎缩蛋白和β-肌营养不良聚糖的表达与定位。共聚焦显微镜显示,PC12细胞核、高尔基体样和内质网样结构中有Dp71d亚型,而Dp71ab集中在神经突尖端和细胞质中,与β-肌营养不良聚糖、抗肌萎缩蛋白、突触小泡蛋白和乙酰胆碱受体共定位。有证据表明,与Dp71d不同,Dp71ab亚型可能参与神经突相关过程。这是关于Dp及其相关蛋白复合物成员在基于细胞系的共培养系统中的作用的第一项研究,这可能有助于确定Dp71亚型的关联。

相似文献

1
Dp71, utrophin and beta-dystroglycan expression and distribution in PC12/L6 cell cocultures.
Neuroreport. 2007 Oct 29;18(16):1657-61. doi: 10.1097/WNR.0b013e3282f0e42d.
5
Dp71ab/DAPs complex composition changes during the differentiation process in PC12 cells.
J Cell Biochem. 2007 Sep 1;102(1):82-97. doi: 10.1002/jcb.21281.
6
Identification of new dystroglycan complexes in skeletal muscle.
PLoS One. 2013 Aug 8;8(8):e73224. doi: 10.1371/journal.pone.0073224. eCollection 2013.
7
Characterization of Dp71Δ(78-79), a novel dystrophin mutant that stimulates PC12 cell differentiation.
J Neurochem. 2011 Nov;119(4):697-707. doi: 10.1111/j.1471-4159.2011.07347.x. Epub 2011 Sep 22.
9
Dystrophin Dp71 is critical for stability of the DAPs in the nucleus of PC12 cells.
Neurochem Res. 2010 Mar;35(3):366-73. doi: 10.1007/s11064-009-0064-z. Epub 2009 Sep 27.
10
Increased expression of dystrophin, beta-dystroglycan and adhalin in denervated rat muscles.
J Muscle Res Cell Motil. 1996 Oct;17(5):523-32. doi: 10.1007/BF00124352.

引用本文的文献

1
Human Dystrophin Dp71ab Enhances the Proliferation of Myoblasts Across Species But Not Human Nonmyoblast Cells.
Front Cell Dev Biol. 2022 Apr 25;10:877612. doi: 10.3389/fcell.2022.877612. eCollection 2022.

本文引用的文献

1
Dystrophin, its interactions with other proteins, and implications for muscular dystrophy.
Biochim Biophys Acta. 2007 Feb;1772(2):108-17. doi: 10.1016/j.bbadis.2006.05.010. Epub 2006 Jun 7.
2
Dissecting the signaling and mechanical functions of the dystrophin-glycoprotein complex.
J Cell Sci. 2006 Apr 15;119(Pt 8):1537-46. doi: 10.1242/jcs.02857. Epub 2006 Mar 28.
3
Structural determinants of alpha4beta2 nicotinic acetylcholine receptor trafficking.
J Neurosci. 2005 Jul 13;25(28):6676-86. doi: 10.1523/JNEUROSCI.1079-05.2005.
4
Dystrophin Dp71 in PC12 cell adhesion.
Neuroreport. 2005 Feb 28;16(3):235-8. doi: 10.1097/00001756-200502280-00006.
5
MuSK is required for anchoring acetylcholinesterase at the neuromuscular junction.
J Cell Biol. 2004 May 24;165(4):505-15. doi: 10.1083/jcb.200307164.
6
Dystrophin Dp71 is required for neurite outgrowth in PC12 cells.
Exp Cell Res. 2004 Jun 10;296(2):265-75. doi: 10.1016/j.yexcr.2004.01.015.
8
Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina.
Hum Mol Genet. 2003 Jul 1;12(13):1543-54. doi: 10.1093/hmg/ddg170.
9
Expression of mouse agrin in normal, denervated and dystrophic muscle.
Neuromuscul Disord. 2003 Jun;13(5):408-15. doi: 10.1016/s0960-8966(03)00036-1.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验