Bai Ruoxue, Liang Baoyan, Guo Yaotao, Liu Wei, Wen Zhuoyue, Wang Zhantong, Zhang Yu, Du Jing, Song Yajuan, Yu Zhou, Ma Xianjie
Department of Plastic and Reconstructive Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Xijing 986 Hospital Department, Fourth Military Medical University, Xi'an, Shaanxi, China.
J Cosmet Dermatol. 2025 Jan;24(1):e16767. doi: 10.1111/jocd.16767.
Tissue expansion is a widely employed technique in reconstructive surgery aimed at addressing considerable skin defects. Nevertheless, matters like inadequate expansion capability and the potential for skin breakage due to the fragility of the expanded tissue present notable hurdles in enhancing skin regeneration during this process. Angiotensin-converting enzyme 2 (ACE2) is recognized for its essential role in facilitating tissue renewal and regeneration. However, its precise impact on skin renewal during tissue expansion remains underexplored. This study seeks to elucidate ACE2's contribution to skin regeneration, specifically examining its role in collagen synthesis.
This study evaluated the expression and distribution of ACE2 in expanded skin using samples derived from both rats and human patients. Additionally, we investigated ACE2 expression in stretched keratinocytes in vitro. ACE2 knockout keratinocytes were transfected with small interfering RNA (siRNA) and cocultured with fibroblasts to observe fibroblast proliferation and migration. MLN-4760 was utilized to inhibit the ACE2 enzymatic activity. Additionally, we analyzed parameters such as the size of expanded skin, dermal thickness, and the levels of collagen I (COL I), collagen III (COL III), and transforming growth factor β (TGF-β) to elucidate the role of ACE2 in the context of expanded skin.
The thinning of the expanded dermis was linked with elevated ACE2 expression. Enzymatic activity and ACE2 expression were both increased by mechanical stress. Additionally, ACE2 utilized Ang II to activate the migration and proliferation of human dermal fibroblasts. In vivo, the ACE2 inhibitor MLN-4760 promoted skin regeneration and reduced dermal thinning by elevating COL I, COL III, and TGF-β during expansion.
This finding suggest that mechanical stretch increases ACE2 expression, which in turn promotes the regeneration of expanded skin. The basis for using ACE2 in clinical settings to increase tissue expansion efficacy is provided by this work.
组织扩张是整形手术中广泛应用的一种技术,旨在解决大面积皮肤缺损问题。然而,在此过程中,诸如扩张能力不足以及由于扩张组织脆弱而导致皮肤破裂的可能性等问题,在促进皮肤再生方面构成了显著障碍。血管紧张素转换酶2(ACE2)因其在促进组织更新和再生中的重要作用而受到认可。然而,其在组织扩张过程中对皮肤更新的确切影响仍未得到充分研究。本研究旨在阐明ACE2对皮肤再生的贡献,特别考察其在胶原蛋白合成中的作用。
本研究使用来自大鼠和人类患者的样本评估ACE2在扩张皮肤中的表达和分布。此外,我们在体外研究了拉伸角质形成细胞中ACE2的表达。用小干扰RNA(siRNA)转染ACE2基因敲除的角质形成细胞,并与成纤维细胞共培养,以观察成纤维细胞的增殖和迁移。使用MLN-4760抑制ACE2的酶活性。此外,我们分析了扩张皮肤的大小、真皮厚度以及I型胶原蛋白(COL I)、III型胶原蛋白(COL III)和转化生长因子β(TGF-β)水平等参数,以阐明ACE2在扩张皮肤背景下的作用。
扩张真皮的变薄与ACE2表达升高有关。机械应力增加了酶活性和ACE2表达。此外,ACE2利用血管紧张素II激活人真皮成纤维细胞的迁移和增殖。在体内,ACE2抑制剂MLN-4760在扩张过程中通过提高COL I、COL III和TGF-β促进皮肤再生并减少真皮变薄。
这一发现表明机械拉伸增加了ACE2表达,进而促进了扩张皮肤的再生。这项工作为在临床环境中使用ACE2提高组织扩张疗效提供了依据。