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本文引用的文献

1
Appendage regeneration in adult vertebrates and implications for regenerative medicine.成年脊椎动物的附肢再生及其对再生医学的意义。
Science. 2005 Dec 23;310(5756):1919-23. doi: 10.1126/science.1115200.
2
Mapping the dominant wound healing and soft tissue regeneration QTL in MRL x CAST.定位MRL与CAST杂交后代中主要的伤口愈合和软组织再生数量性状位点。
Mamm Genome. 2005 Dec;16(12):918-24. doi: 10.1007/s00335-005-0077-0. Epub 2005 Dec 8.
3
Physical enhancement of transdermal drug application: is delivery technology keeping up with pharmaceutical development?经皮给药的物理增强:给药技术是否跟上了药物研发的步伐?
Curr Drug Deliv. 2004 Jan;1(1):81-92. doi: 10.2174/1567201043480045.
4
Accelerated wound healing of alkali-burned corneas in MRL mice is associated with a reduced inflammatory signature.MRL小鼠碱烧伤角膜伤口愈合加速与炎症特征减轻有关。
Invest Ophthalmol Vis Sci. 2005 Nov;46(11):4097-106. doi: 10.1167/iovs.05-0548.
5
New quantitative trait loci that regulate wound healing in an intercross progeny from DBA/1J and 129 x 1/SvJ inbred strains of mice.调控DBA/1J和129×1/SvJ近交系小鼠杂交后代伤口愈合的新数量性状基因座。
Funct Integr Genomics. 2006 Apr;6(2):157-63. doi: 10.1007/s10142-005-0004-1. Epub 2005 Oct 6.
6
First experience of the use bone marrow mesenchymal stem cells for the treatment of a patient with deep skin burns.使用骨髓间充质干细胞治疗一名深度皮肤烧伤患者的首次经验。
Bull Exp Biol Med. 2005 Jan;139(1):141-4. doi: 10.1007/s10517-005-0232-3.
7
Human mesenchymal stem cells successfully improve skin-substitute wound healing.人间充质干细胞成功改善皮肤替代物伤口愈合。
Br J Dermatol. 2005 Jul;153(1):29-36. doi: 10.1111/j.1365-2133.2005.06554.x.
8
"Xenograft" dressing in the treatment of burns.“异种移植”敷料在烧伤治疗中的应用
Clin Dermatol. 2005 Jul-Aug;23(4):419-23. doi: 10.1016/j.clindermatol.2004.07.027.
9
Harnessing wound healing and regeneration for tissue engineering.利用伤口愈合与再生进行组织工程
Biochem Soc Trans. 2005 Apr;33(Pt 2):413-7. doi: 10.1042/BST0330413.
10
Stem cell transplantation therapy: controversy over ethical issues and clinical relevance.干细胞移植疗法:关于伦理问题和临床相关性的争议。
Drug News Perspect. 2004 Dec;17(10):637-45. doi: 10.1358/dnp.2004.17.10.873915.

表征脊椎动物耳朵中的再生现象。

Characterizing regeneration in the vertebrate ear.

作者信息

Metcalfe Anthony D, Willis Hayley, Beare Alice, Ferguson Mark W J

机构信息

UK Centre for Tissue Engineering, Faculty of Life Sciences, University of Manchester, UK.

出版信息

J Anat. 2006 Oct;209(4):439-46. doi: 10.1111/j.1469-7580.2006.00632.x.

DOI:10.1111/j.1469-7580.2006.00632.x
PMID:17005017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2100363/
Abstract

We have previously shown that MRL/MpJ mice have a capacity for regeneration instead of scar formation following an ear punch wound. Understanding the differences that occur between scar-free regeneration or repair with scarring will have great impact upon advances in skin tissue engineering. A key question that remains unanswered in the MRL/MpJ mouse model is whether regeneration was restricted to the ear or whether it extended to the skin. A histological analysis was conducted up to 4 months post-wounding, not only with 2-mm punch wounds to the ear but also to the skin on the backs of the same animals. MRL/MpJ mouse ear wounds regenerate faster than control strains, with enhanced blastema formation, a markedly thickened tip epithelium and reduced scarring. Interestingly, in the excisional back wounds, none of these regenerative features was observed and both the C57BL/6 control and MRL/MpJ mice healed with scarring. This review gives an insight into how this regenerative capacity may be due to evolutionary processes as well as ear anatomy. The ear is thin and surrounded on both sides by epithelia, and the dorsal skin is devoid of cartilage and under greater tensile strain. Analysis of apoptosis during ear regeneration is also discussed, assessing the role and expression of various members of the Bcl-2 family of proteins. Ongoing studies are focusing on de novo cartilage development in the regenerating ear, as well as understanding the role of downstream signalling cascades in the process. Identification of such signals could lead to their manipulation and use in a novel tissue-engineered skin substitute with scar-free integration.

摘要

我们之前已经表明,MRL/MpJ小鼠在耳部打孔创伤后具有再生能力而非瘢痕形成能力。了解无瘢痕再生或瘢痕修复之间的差异,将对皮肤组织工程的进展产生重大影响。在MRL/MpJ小鼠模型中,一个尚未得到解答的关键问题是,再生是否仅限于耳部,还是也延伸至皮肤。我们对创伤后长达4个月的情况进行了组织学分析,不仅对耳部进行了2毫米的打孔创伤,还对同一动物背部的皮肤进行了创伤。MRL/MpJ小鼠耳部伤口的再生速度比对照品系更快,芽基形成增强,尖端上皮明显增厚,瘢痕形成减少。有趣的是,在背部切除伤口中,未观察到这些再生特征,C57BL/6对照小鼠和MRL/MpJ小鼠均通过瘢痕愈合。这篇综述深入探讨了这种再生能力可能是由于进化过程以及耳部解剖结构所致。耳部较薄,两侧被上皮包围,背部皮肤没有软骨且承受更大的拉伸应变。本文还讨论了耳部再生过程中的细胞凋亡分析,评估了Bcl-2蛋白家族各成员的作用和表达。正在进行的研究聚焦于再生耳部的软骨从头发育,以及了解下游信号级联在该过程中的作用。识别这些信号可能会促使人们对其进行操控,并将其应用于一种新型的、能无瘢痕整合的组织工程皮肤替代物中。