From the Hagey Laboratory for Pediatric Regenerative Medicine.
Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine.
Plast Reconstr Surg. 2024 Jan 1;153(1):121-128. doi: 10.1097/PRS.0000000000010465. Epub 2023 Mar 27.
A significant gap exists in the translatability of small-animal models to human subjects. One important factor is poor laboratory models involving human tissue. Thus, the authors have created a viable postnatal human skin xenograft model using athymic mice.
Discarded human foreskins were collected following circumcision. All subcutaneous tissue was removed from these samples sterilely. Host CD-1 nude mice were then anesthetized, and dorsal skin was sterilized. A 1.2-cm-diameter, full-thickness section of dorsal skin was excised. The foreskin sample was then placed into the full-thickness defect in the host mice and sutured into place. Xenografts underwent dermal wounding using a 4-mm punch biopsy after engraftment. Xenografts were monitored for 14 days after wounding and then harvested.
At 14 days postoperatively, all mice survived the procedure. Grossly, the xenograft wounds showed formation of a human scar at postoperative day 14. Hematoxylin and eosin and Masson trichome staining confirmed scar formation in the wounded human skin. Using a novel artificial intelligence algorithm using picrosirius red staining, scar formation was confirmed in human wounded skin compared with the unwounded skin. Histologically, CD31 + immunostaining confirmed vascularization of the xenograft. The xenograft exclusively showed human collagen type I, CD26 + , and human nuclear antigen in the human scar without any staining of these human markers in the murine skin.
The proposed model demonstrates wound healing to be a local response from tissue resident human fibroblasts and allows for reproducible evaluation of human skin wound repair in a preclinical model.
Radiation-induced fibrosis is a widely prevalent clinical phenomenon without a well-defined treatment at this time. This study will help establish a small-animal model to better understand and develop novel therapeutics to treat irradiated human skin.
小动物模型转化为人体存在显著差距。一个重要因素是涉及人体组织的实验室模型较差。因此,作者使用无胸腺鼠创建了可行的产后人皮移植模型。
收集包皮环切术后丢弃的人包皮。无菌去除这些样本中的所有皮下组织。然后使宿主 CD-1 裸鼠麻醉,并对背部皮肤进行消毒。切除 1.2 厘米直径的全厚背部皮肤。然后将包皮样本放入宿主小鼠的全厚缺陷处并缝合到位。移植后,使用 4 毫米打孔活检对异种移植物进行真皮创伤。创伤后 14 天监测异种移植物,然后收获。
术后 14 天,所有小鼠均存活。大体上,异种移植物伤口在术后第 14 天显示出人类疤痕的形成。苏木精和伊红以及 Masson 三色染色证实了受伤人皮中的疤痕形成。使用使用 picrosirius 红染色的新型人工智能算法,与未受伤的皮肤相比,在受伤的人皮中确认了疤痕形成。组织学上,CD31+免疫染色证实了异种移植物的血管生成。异种移植物仅在人类疤痕中显示人类胶原 I 型、CD26+和人类核抗原,而在鼠皮中没有这些人类标志物的染色。
所提出的模型表明伤口愈合是组织驻留的人类成纤维细胞的局部反应,并允许在临床前模型中可重复地评估人类皮肤伤口修复。
放射性纤维化是一种广泛存在的临床现象,目前尚无明确的治疗方法。本研究将有助于建立小动物模型,以更好地理解和开发治疗放射性人类皮肤的新疗法。