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本文引用的文献

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Chondroitinase injection improves keloid pathology by reorganizing the extracellular matrix with regenerated elastic fibers.注射软骨素酶通过再生弹性纤维来重组细胞外基质,从而改善瘢痕疙瘩的病理。
J Dermatol. 2013 May;40(5):380-3. doi: 10.1111/1346-8138.12116. Epub 2013 Mar 4.
2
A novel three-dimensional model system for keloid study: organotypic multicellular scar model.一种用于瘢痕疙瘩研究的新型三维模型系统:器官型多细胞瘢痕模型。
Wound Repair Regen. 2013 Jan-Feb;21(1):155-65. doi: 10.1111/j.1524-475X.2012.00869.x. Epub 2012 Dec 11.
3
Establishment of an animal model for human keloid scars using tissue engineering method.利用组织工程方法建立人瘢痕疙瘩的动物模型。
J Burn Care Res. 2013 Jul-Aug;34(4):439-46. doi: 10.1097/BCR.0b013e318269bd64.
4
Current concepts in the etiology and treatment of keloids.瘢痕疙瘩病因及治疗的当前概念
Facial Plast Surg. 2012 Oct;28(5):504-12. doi: 10.1055/s-0032-1325644. Epub 2012 Oct 1.
5
An ex vivo model employing keloid-derived cell-seeded collagen sponges for therapy development.采用瘢痕疙瘩来源的细胞接种胶原海绵的体外模型用于治疗开发。
J Invest Dermatol. 2013 Feb;133(2):386-93. doi: 10.1038/jid.2012.314. Epub 2012 Sep 6.
6
Keloid scarring: understanding the genetic basis, advances, and prospects.瘢痕疙瘩形成:了解其遗传基础、进展及前景
Arch Plast Surg. 2012 May;39(3):184-9. doi: 10.5999/aps.2012.39.3.184. Epub 2012 May 10.
7
Deep and superficial keloid fibroblasts contribute differentially to tissue phenotype in a novel in vivo model of keloid scar.深、浅层瘢痕疙瘩成纤维细胞在瘢痕疙瘩的新型体内模型中对组织表型的贡献不同。
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Long-term organ culture of keloid disease tissue.瘢痕疙瘩病组织的长期器官培养。
Exp Dermatol. 2012 May;21(5):376-81. doi: 10.1111/j.1600-0625.2012.01476.x.
9
miR-196a downregulation increases the expression of type I and III collagens in keloid fibroblasts.miR-196a 的下调增加了瘢痕疙瘩成纤维细胞中 I 型和 III 型胶原的表达。
J Invest Dermatol. 2012 Jun;132(6):1597-604. doi: 10.1038/jid.2012.22. Epub 2012 Feb 23.
10
Therapeutic potential of fibroblast growth factor-2 for hypertrophic scars: upregulation of MMP-1 and HGF expression.成纤维细胞生长因子-2 治疗增生性瘢痕的潜力:基质金属蛋白酶-1 和肝细胞生长因子表达的上调。
Lab Invest. 2012 Feb;92(2):214-23. doi: 10.1038/labinvest.2011.127. Epub 2011 Sep 26.

异常瘢痕形成模型。

Models of abnormal scarring.

机构信息

Department of Plastic and Reconstructive Surgery, Uijeongbu St. Mary's Hospital, College of Medicine, Catholic University of Korea, 65-1 Kumoh-Dong, Uijeongbu 480-135, Republic of Korea.

出版信息

Biomed Res Int. 2013;2013:423147. doi: 10.1155/2013/423147. Epub 2013 Sep 3.

DOI:10.1155/2013/423147
PMID:24078916
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3775400/
Abstract

Keloids and hypertrophic scars are thick, raised dermal scars, caused by derailing of the normal scarring process. Extensive research on such abnormal scarring has been done; however, these being refractory disorders specific to humans, it has been difficult to establish a universal animal model. A wide variety of animal models have been used. These include the athymic mouse, rats, rabbits, and pigs. Although these models have provided valuable insight into abnormal scarring, there is currently still no ideal model. This paper reviews the models that have been developed.

摘要

瘢痕疙瘩和增生性瘢痕是由正常瘢痕形成过程脱轨引起的厚的、隆起的皮肤瘢痕。已经对这种异常瘢痕进行了广泛的研究;然而,由于这些是人类特有的难治性疾病,因此很难建立通用的动物模型。已经使用了各种各样的动物模型。这些模型包括无胸腺小鼠、大鼠、兔子和猪。尽管这些模型为异常瘢痕的形成提供了有价值的见解,但目前仍然没有理想的模型。本文综述了已经开发的模型。