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Tissue Profiling by MALDI Mass Spectrometry Distinguishes Clinical Grades of Soft Tissue Sarcomas.通过基质辅助激光解吸电离质谱法进行组织分析可区分软组织肉瘤的临床分级。
Cancer Genomics Proteomics. 2005 Nov-Dec;2(6):333-345. Epub 2005 Nov 1.
2
Skin wounds in the MRL/MPJ mouse heal with scar.MRL/MPJ小鼠的皮肤伤口会形成瘢痕愈合。
Wound Repair Regen. 2006 Jan-Feb;14(1):81-90. doi: 10.1111/j.1524-475X.2005.00092.x.
3
Intracellular calcium-binding protein S100A4 influences injury-induced migration of white matter astrocytes.细胞内钙结合蛋白S100A4影响损伤诱导的白质星形胶质细胞迁移。
Acta Neuropathol. 2006 Mar;111(3):213-9. doi: 10.1007/s00401-005-0019-7. Epub 2006 Feb 4.
4
Proteomic patterns and prediction of glomerulosclerosis and its mechanisms.蛋白质组学模式与肾小球硬化的预测及其机制
J Am Soc Nephrol. 2005 Oct;16(10):2967-75. doi: 10.1681/ASN.2005030262. Epub 2005 Aug 3.
5
Direct profiling of the cerebellum by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry: A methodological study in postnatal and adult mouse.
J Neurosci Res. 2005 Sep 1;81(5):613-21. doi: 10.1002/jnr.20590.
6
FGF-2, IL-1beta and TGF-beta regulate fibroblast expression of S100A8.成纤维细胞生长因子-2、白细胞介素-1β和转化生长因子-β调节S100A8在成纤维细胞中的表达。
FEBS J. 2005 Jun;272(11):2811-27. doi: 10.1111/j.1742-4658.2005.04703.x.
7
Characterization of G-banded chromosomes of a female saola (Pseudoryx nghetinhensis,2n = 50) and X chromosome i dentification by means of fluorescent in situ hybridization.
Cytogenet Genome Res. 2005;109(4):502-6. doi: 10.1159/000084210.
8
MRL mice fail to heal the heart in response to ischemia-reperfusion injury.MRL小鼠在面对缺血再灌注损伤时无法使心脏愈合。
Wound Repair Regen. 2005 Mar-Apr;13(2):205-8. doi: 10.1111/j.1067-1927.2005.130212.x.
9
Tissue profiling by mass spectrometry: a review of methodology and applications.基于质谱的组织分析:方法与应用综述
Mol Cell Proteomics. 2005 Apr;4(4):394-401. doi: 10.1074/mcp.R500006-MCP200. Epub 2005 Jan 26.
10
Early changes in protein expression detected by mass spectrometry predict tumor response to molecular therapeutics.通过质谱检测到的蛋白质表达早期变化可预测肿瘤对分子疗法的反应。
Cancer Res. 2004 Dec 15;64(24):9093-100. doi: 10.1158/0008-5472.CAN-04-2231.

组织轮廓分析基质辅助激光解吸电离质谱法揭示了再生型MRL小鼠伤口蛋白质组中显著的钙结合蛋白。

Tissue profiling MALDI mass spectrometry reveals prominent calcium-binding proteins in the proteome of regenerative MRL mouse wounds.

作者信息

Caldwell Robert L, Opalenik Susan R, Davidson Jeffrey M, Caprioli Richard M, Nanney Lillian B

机构信息

Vanderbilt Orthopaedic Institute, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.

出版信息

Wound Repair Regen. 2008 May-Jun;16(3):442-9. doi: 10.1111/j.1524-475X.2007.00351.x. Epub 2008 Feb 13.

DOI:10.1111/j.1524-475X.2007.00351.x
PMID:18282264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2891803/
Abstract

MRL/MpJ-Fas(lpr) mice exhibit the ability to regenerate ear tissue excised by dermal punches. This is an exceptional model to identify candidate proteins that may regulate regeneration in typically nonregenerative tissues. Identification of key molecules involved in regeneration can broaden our understanding of the wound-healing process and generate novel therapeutic approaches. Tissue profiling by matrix-assisted laser desorption ionization mass spectrometry is a rapid, powerful proteomic tool that allows hundreds of proteins to be detected from specific regions of intact tissue specimens. To identify these candidate molecules, protein expression in ear punches was examined after 4 and 7 days using tissue profiling of MRL/MpJ-Fas(lpr) mice and the nonregenerative mouse strain C57BL/6J. Spectral analysis revealed distinct proteomic differences between the regenerative and nonregenerative phenotypes, including the calcium-binding proteins calgranulin A and B, calgizzarin, and calmodulin. Spatial distributions for these differentially expressed proteins within the injured regions were confirmed by immunohistochemistry.

摘要

MRL/MpJ-Fas(lpr)小鼠表现出再生经皮肤打孔切除的耳部组织的能力。这是一个用于鉴定可能调节典型非再生组织再生的候选蛋白质的特殊模型。鉴定参与再生的关键分子可以拓宽我们对伤口愈合过程的理解,并产生新的治疗方法。基质辅助激光解吸电离质谱法进行的组织分析是一种快速、强大的蛋白质组学工具,可从完整组织标本的特定区域检测数百种蛋白质。为了鉴定这些候选分子,使用MRL/MpJ-Fas(lpr)小鼠和非再生小鼠品系C57BL/6J的组织分析,在4天和7天后检查耳部打孔处的蛋白质表达。光谱分析揭示了再生和非再生表型之间明显的蛋白质组差异,包括钙结合蛋白钙粒蛋白A和B、钙结合蛋白、钙调蛋白。通过免疫组织化学证实了这些差异表达蛋白在损伤区域内的空间分布。