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2
Deregulation of keratinocyte differentiation and activation: a hallmark of venous ulcers.角质形成细胞分化和激活失调:静脉溃疡的一个标志。
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3
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Numerous keratinocyte subtypes involved in wound re-epithelialization.多种角质形成细胞亚型参与伤口再上皮化过程。
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本文引用的文献

1
K16 is a further new candidate for homotypic intermediate filament protein interactions.K16 是同种型中间丝蛋白相互作用的另一个新候选蛋白。
Exp Dermatol. 2010 Aug;19(8):e241-50. doi: 10.1111/j.1600-0625.2010.01071.x.
2
Aberrant heterodimerization of keratin 16 with keratin 6A in HaCaT keratinocytes results in diminished cellular migration.在 HaCaT 角质细胞中,角蛋白 16 与角蛋白 6A 的异常异二聚化导致细胞迁移减少。
Mech Ageing Dev. 2010 May;131(5):346-53. doi: 10.1016/j.mad.2010.04.002. Epub 2010 Apr 18.
3
Replacement of animal-derived collagen matrix by human fibroblast-derived dermal matrix for human skin equivalent products.用人成纤维细胞衍生的真皮基质替代动物源性胶原蛋白基质,用于人皮肤等效产品。
Biomaterials. 2009 Jan;30(1):71-8. doi: 10.1016/j.biomaterials.2008.09.002. Epub 2008 Oct 5.
4
Development of an in vitro burn wound model.体外烧伤创面模型的建立。
Wound Repair Regen. 2008 Jul-Aug;16(4):559-67. doi: 10.1111/j.1524-475X.2008.00403.x.
5
Deregulation of keratinocyte differentiation and activation: a hallmark of venous ulcers.角质形成细胞分化和激活失调:静脉溃疡的一个标志。
J Cell Mol Med. 2008 Dec;12(6B):2675-90. doi: 10.1111/j.1582-4934.2008.00321.x. Epub 2008 Mar 28.
6
Migration of the epidermal over the dermal component (epiboly) in a bilayered bioengineered skin construct.在双层生物工程皮肤构建物中,表皮在真皮成分上的迁移(外包)。
Tissue Eng. 2007 Jan;13(1):21-8. doi: 10.1089/ten.2006.0148.
7
A keratin cytoskeletal protein regulates protein synthesis and epithelial cell growth.一种角蛋白细胞骨架蛋白调节蛋白质合成和上皮细胞生长。
Nature. 2006 May 18;441(7091):362-5. doi: 10.1038/nature04659.
8
Cytokeratin, filaggrin, and p63 expression in reepithelialization during human cutaneous wound healing.细胞角蛋白、丝聚蛋白和p63在人类皮肤伤口愈合再上皮化过程中的表达
Wound Repair Regen. 2006 Jan-Feb;14(1):38-45. doi: 10.1111/j.1743-6109.2005.00086.x.
9
Epithelial regeneration from bioengineered skin explants in culture.培养物中生物工程皮肤外植体的上皮再生。
Br J Dermatol. 2006 Jan;154(1):42-9. doi: 10.1111/j.1365-2133.2005.06997.x.
10
Numerous keratinocyte subtypes involved in wound re-epithelialization.多种角质形成细胞亚型参与伤口再上皮化过程。
J Invest Dermatol. 2006 Feb;126(2):497-502. doi: 10.1038/sj.jid.5700101.

生物工程皮肤伤口模型和人类慢性伤口中外胚层形成过程中的角蛋白差异表达。

Differential keratin expression during epiboly in a wound model of bioengineered skin and in human chronic wounds.

作者信息

Luo Su, Yufit Tatyana, Carson Polly, Fiore David, Falanga Jane, Lin Xiaofeng, Mamakos Lisa, Falanga Vincent

机构信息

Roger Williams Medical Center, Providence, RI 02908, USA.

出版信息

Int J Low Extrem Wounds. 2011 Sep;10(3):122-9. doi: 10.1177/1534734611418157. Epub 2011 Aug 19.

DOI:10.1177/1534734611418157
PMID:21856973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4082561/
Abstract

Epiboly represents the process by which keratinocytes migrate to envelop a surface. The authors have been investigating a living bilayered skin construct (BSC) that is used in the treatment of lower extremity wounds due to venous insufficiency and diabetes. The construct demonstrates epiboly after injury and incubation in vitro, and this model may be useful for studying epidermal migration and the process of skin maturation. Punch biopsies of the construct in vitro were cultured and immunostained for specific keratins at baseline and at 24 to 72 hours. For comparison, skin biopsy specimens from human chronic venous ulcers and acute healing wounds were similarly processed. The authors found that K1 and K10 were fully expressed in the epidermis of the fully epibolized surface on BSC. K1 was also present in the migrating edge of specimens, whereas K10 was not detectable. K16 and K6 were evident in normal skin and the epibolized area of the construct; K6 expression was very prominent in the migrating edge. Importantly, K17 was distinctly limited to the epibolized surface and the migrating edge, and its expression was very similar to that observed in healing human wounds. In conclusion, differential expression of keratins in this epiboly model closely reflects in vivo studies and supports keratin specificity in the processes of migration and differentiation of new epidermis. Therefore, these findings provide further and important validity for the study of epithelialization and the hope of developing prognostic markers for venous ulcer healing.

摘要

表皮细胞迁移是角质形成细胞迁移以覆盖表面的过程。作者一直在研究一种用于治疗因静脉功能不全和糖尿病导致的下肢伤口的活性双层皮肤构建体(BSC)。该构建体在体外损伤和孵育后表现出表皮细胞迁移,并且该模型可能有助于研究表皮迁移和皮肤成熟过程。对体外构建体的打孔活检组织在基线以及24至72小时进行培养并针对特定角蛋白进行免疫染色。作为对照,对来自人类慢性静脉溃疡和急性愈合伤口的皮肤活检标本进行类似处理。作者发现,在BSC完全表皮细胞迁移化表面的表皮中,K1和K10充分表达。K1也存在于标本的迁移边缘,而未检测到K10。K16和K6在正常皮肤和构建体的表皮细胞迁移化区域中明显可见;K6在迁移边缘的表达非常突出。重要的是,K17明显局限于表皮细胞迁移化表面和迁移边缘,其表达与在人类愈合伤口中观察到的非常相似。总之,在这个表皮细胞迁移模型中角蛋白的差异表达密切反映了体内研究,并支持新表皮迁移和分化过程中的角蛋白特异性。因此,这些发现为上皮形成研究提供了进一步的重要依据,并为开发静脉溃疡愈合的预后标志物带来了希望。