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[通过将人瘢痕疙瘩移植到裸鼠背部建立瘢痕疙瘩模型]

[Establishment of a keloid model by transplanting human keloid onto the backs of nude mice].

作者信息

Philandrianos C, Gonnelli D, Andrac-Meyer L, Bruno M, Magalon G, Mordon S

机构信息

Service de chirurgie plastique et maxillofacial, hôpital Nord de Marseille, chemin des Bourrely, 13915 Marseille cedex, France; Inserm U 703, 152, rue du Dr.-Yersin, 59120 Loos, France.

Service de chirurgie plastique et maxillofacial, hôpital Nord de Marseille, chemin des Bourrely, 13915 Marseille cedex, France.

出版信息

Ann Chir Plast Esthet. 2014 Aug;59(4):246-52. doi: 10.1016/j.anplas.2012.05.001. Epub 2012 Jun 12.

DOI:10.1016/j.anplas.2012.05.001
PMID:22699002
Abstract

Keloid scar is a proliferative healing dysfunction formed by an excessive build-up of collagen fibers on the dermis. It is responsible of aesthetic and functional disabilities. There is no ideal treatment and recurrence occurs very often. Keloid scars occur only to human, that's why animal model needs to be made to study this pathology and new treatments. Few models have been described using human keloid scars implanted into subcutaneous tissue of nude mice or rat. To allow study of topical and laser treatment we have developed a new animal model using human keloid scar fragment with epidermal and dermal tissue implanted into back of nude mice like a full thickness skin graft. Keloid fragments from five donors have been grafted onto 40 nudes mice. Macroscopic and microscopic studies have been made at day 28, 56, 84 and 112. We observed integration of the fragments in all cases. Hyalinized collagen bundles were observed in all implant biopsies confirming the stability of the keloid architecture within 112 days. This model is easily reproducible and allows the study of topical treatment and laser due to the accessibility of the keloid.

摘要

瘢痕疙瘩是一种增殖性愈合功能障碍,由真皮层胶原纤维过度堆积形成。它会导致美观和功能障碍。目前尚无理想的治疗方法,且复发很常见。瘢痕疙瘩仅发生于人类,因此需要建立动物模型来研究这种病理情况和新的治疗方法。很少有模型描述将人类瘢痕疙瘩植入裸鼠或大鼠的皮下组织。为了能够研究局部治疗和激光治疗,我们开发了一种新的动物模型,将带有表皮和真皮组织的人类瘢痕疙瘩碎片像全层皮肤移植一样植入裸鼠背部。来自五名捐赠者的瘢痕疙瘩碎片已移植到40只裸鼠身上。在第28天、56天、84天和112天进行了宏观和微观研究。我们观察到在所有情况下碎片均已整合。在所有植入活检中均观察到透明化的胶原束,证实了瘢痕疙瘩结构在112天内的稳定性。该模型易于复制,并且由于瘢痕疙瘩易于触及,因此可以用于研究局部治疗和激光治疗。

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[Establishment of a keloid model by transplanting human keloid onto the backs of nude mice].[通过将人瘢痕疙瘩移植到裸鼠背部建立瘢痕疙瘩模型]
Ann Chir Plast Esthet. 2014 Aug;59(4):246-52. doi: 10.1016/j.anplas.2012.05.001. Epub 2012 Jun 12.
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Establishment of a hypertrophic scar model by transplanting full-thickness human skin grafts onto the backs of nude mice.通过将人全层皮肤移植到裸鼠背部建立肥厚性瘢痕模型。
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Keloid-derived, plasma/fibrin-based skin equivalents generate de novo dermal and epidermal pathology of keloid fibrosis in a mouse model.在小鼠模型中,瘢痕疙瘩来源的、基于血浆/纤维蛋白的皮肤替代物会产生瘢痕疙瘩纤维化的新生真皮和表皮病理变化。
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[Replication of pathological scar in nude mice].[病理性瘢痕在裸鼠体内的复制]
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Human hypertrophic scar-like nude mouse model: characterization of the molecular and cellular biology of the scar process.人增生性瘢痕样裸鼠模型:瘢痕形成过程的分子和细胞生物学特征。
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Treatment of keloid scars with a 1210-nm diode laser in an animal model.在动物模型中用1210纳米二极管激光治疗瘢痕疙瘩。
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Treatment of Keloid Scars with Botulinum Toxin Type A versus Triamcinolone in an Athymic Nude Mouse Model.A型肉毒毒素与曲安奈德治疗无毛小鼠瘢痕疙瘩的比较。
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[Keloid scars: a case series study].[瘢痕疙瘩:病例系列研究]
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A nude mouse model of hypertrophic scar shows morphologic and histologic characteristics of human hypertrophic scar.增生性瘢痕裸鼠模型显示出人类增生性瘢痕的形态和组织学特征。
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Implantation of human keloid into athymic mice.将人类瘢痕疙瘩植入无胸腺小鼠体内。
Laryngoscope. 1987 Oct;97(10):1214-8. doi: 10.1288/00005537-198710000-00018.

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Inhibition of growth of Asian keloid cells with human umbilical cord Wharton's jelly stem cell-conditioned medium.人脐带华通氏胶干细胞条件培养基抑制亚洲瘢痕疙瘩细胞生长。
Stem Cell Res Ther. 2020 Feb 21;11(1):78. doi: 10.1186/s13287-020-01609-7.
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Regeneration of Dermis: Scarring and Cells Involved.皮肤组织再生:疤痕和涉及的细胞。
Cells. 2019 Jun 18;8(6):607. doi: 10.3390/cells8060607.