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用培养的同种异体角质形成细胞片治疗手术伤口后愈合过程中的表皮分化和真皮变化。

Epidermal differentiation and dermal changes in healing following treatment of surgical wounds with sheets of cultured allogeneic keratinocytes.

作者信息

Myers S R, Navsaria H A, Brain A N, Purkis P E, Leigh I M

机构信息

Department of Experimental Dermatology, Royal London Hospital.

出版信息

J Clin Pathol. 1995 Dec;48(12):1087-92. doi: 10.1136/jcp.48.12.1087.

DOI:10.1136/jcp.48.12.1087
PMID:8567992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC503032/
Abstract

AIMS

To establish the structural changes that occur in deep surgical wounds engrafted with allogeneic sheets, their time course and inter-relation.

METHODS

Deep surgical wounds following shave excision of tattoos (down to deep dermis/subcutaneous fat) were treated with sheets of sex mismatched allogeneic keratinocytes in 19 patients and then biopsied weekly until wound healing was complete. More superficial surgical wounds--that is, 20 standard skin graft donor sites, were biopsied at seven to 10 days (all healed) following application of keratinocyte allografts. All biopsy specimens were examined with a large panel of monoclonal antibodies to keratins, envelope proteins, basement membrane components, and to extracellular matrix components.

RESULTS

The hyperproliferative keratin pair K6/16 was expressed in all wounds, for up to six weeks in keratinocyte grafted deep wounds, and up to six months in split thickness skin grafted wounds.

CONCLUSIONS

Keratins 6 and 16 have not been detected in normal skin, although the relevant mRNA has. This raises the possibility of regulation at a post-transcriptional level allowing a rapid response to injury with cytoskeletal changes that may aid cell migration. This keratin pair offers the most sensitive marker for altered epidermis following wounding.

摘要

目的

确定植入异体薄片的深部手术伤口所发生的结构变化、其时间进程及相互关系。

方法

对19例纹身剃除术后的深部手术伤口(直至真皮深层/皮下脂肪)用性别不匹配的异体角质形成细胞薄片进行治疗,然后每周进行活检直至伤口完全愈合。对20个标准皮肤移植供区等更表浅的手术伤口,在应用异体角质形成细胞移植后7至10天(均已愈合)进行活检。所有活检标本均用一大组针对角蛋白、包膜蛋白、基底膜成分及细胞外基质成分的单克隆抗体进行检测。

结果

增殖性角蛋白对K6/16在所有伤口中均有表达,在植入角质形成细胞的深部伤口中持续表达长达六周,在中厚皮片移植伤口中持续表达长达六个月。

结论

尽管在正常皮肤中未检测到角蛋白6和16,但相关mRNA已被检测到。这增加了在转录后水平进行调控的可能性,从而允许对损伤做出快速反应,伴随细胞骨架变化,这可能有助于细胞迁移。这对角蛋白对是伤口后表皮改变最敏感的标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/2aad608751af/jclinpath00237-0018-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/22d542304824/jclinpath00237-0017-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/812036ad207a/jclinpath00237-0017-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/2b8d2fd738d1/jclinpath00237-0017-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/1e1f8b06c147/jclinpath00237-0018-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/53a44a152300/jclinpath00237-0018-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/2aad608751af/jclinpath00237-0018-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/22d542304824/jclinpath00237-0017-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/812036ad207a/jclinpath00237-0017-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/2b8d2fd738d1/jclinpath00237-0017-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/1e1f8b06c147/jclinpath00237-0018-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/53a44a152300/jclinpath00237-0018-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c92/503032/2aad608751af/jclinpath00237-0018-c.jpg

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Monospecific monoclonal antibodies to keratin 1 carboxy terminal (synthetic peptide) and to keratin 10 as markers of epidermal differentiation.针对角蛋白1羧基末端(合成肽)和角蛋白10的单特异性单克隆抗体,作为表皮分化的标志物。
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