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对面部暴露皮肤有皱纹或无皱纹区域以及未暴露皮肤进行转录组学和组织学分析。

Transcriptomic and histological analysis of exposed facial skin areas wrinkled or not and unexposed skin.

作者信息

Martin Renan Paulo, Varela Patricia, Gomes Caio Peres, Marins Maryana Mara, Filippelli-Silva Rafael, Yarak Samira, Soares Juliana L M, Sanudo Adriana, Idkowiak-Baldys Jolanta, Chen Siming, Hwang Cheng, Zhuang Yong, Lyga John, Pesquero João Bosco, Bagatin Edileia

机构信息

McKusick-Nathans Department of Genetic Medicine, Johns Hopkins School of Medicine, Baltimore, MD, 21205, USA.

Department of Biophysics, Universidade Federal de Sao Paulo, São Paulo, Brazil.

出版信息

Mol Biol Rep. 2022 Mar;49(3):1669-1678. doi: 10.1007/s11033-021-06973-y. Epub 2021 Dec 1.

Abstract

BACKGROUND

Skin aging involves genetic, environmental and hormonal factors. Facial wrinkles also depend on muscular activity. Gene expression investigation may be useful for new anti-aging products.

METHODS AND RESULTS

To evaluate structure and gene expression differences among exposed and unexposed skin in menopausal women. Cross-sectional study, including 15 menopausal women, 55-65 years, phototype III; photo-exposed, periorbital wrinkles (A1), preauricular, not wrinkled (A2), and unexposed gluteal (A3) areas were described and compared by non-invasive measures, histology, immunohistochemistry and gene expression (RNASeq); participants mean age was 61yo, presenting moderate periorbital wrinkles and light facial photodamage. Higher roughness, wrinkles number and echogenicity were observed in A1 and A2 versus A3. Decreased epidermal thickness and dermal collagen IV were demonstrated in A1 versus A2 and A3. Exposed areas impacted different pathways compared to unexposed. Exposed wrinkled skin (A1) showed impact on cell movement with decreased inflammatory activation state. Pathways related to lipid and aminoacids metabolism were modulated in non-wrinkled exposed (A2) compared to unexposed (A3) skin.

CONCLUSIONS

Expected histological findings and gene expression differences among areas were observed. Photoaging in menopausal women may modulate lipid and aminoacids metabolism and decrease inflammatory and keratinization pathways, cellular homeostasis, immune response, fibrogenesis and filament formation. These findings may help development of new therapies for skin health and aging control.

摘要

背景

皮肤老化涉及遗传、环境和激素因素。面部皱纹也取决于肌肉活动。基因表达研究可能有助于新型抗衰老产品的研发。

方法与结果

评估绝经后女性暴露皮肤和未暴露皮肤之间的结构及基因表达差异。横断面研究,纳入15名年龄在55 - 65岁、皮肤光类型为III型的绝经后女性;对光暴露的眶周皱纹区域(A1)、耳前未出现皱纹区域(A2)以及未暴露的臀肌区域(A3)进行描述,并通过非侵入性测量、组织学、免疫组织化学和基因表达(RNA测序)进行比较;参与者的平均年龄为61岁,眶周有中度皱纹且面部有轻度光损伤。与A3相比,A1和A2区域的粗糙度、皱纹数量和回声性更高。与A2和A3相比,A1区域的表皮厚度和真皮IV型胶原蛋白减少。与未暴露区域相比,暴露区域影响不同的信号通路。暴露的皱纹皮肤(A1)对细胞运动有影响,炎症激活状态降低。与未暴露(A3)皮肤相比,未出现皱纹的暴露区域(A2)中与脂质和氨基酸代谢相关的信号通路受到调节。

结论

观察到各区域预期的组织学结果和基因表达差异。绝经后女性的光老化可能会调节脂质和氨基酸代谢,减少炎症和角质形成信号通路、细胞内稳态、免疫反应、纤维生成和细丝形成。这些发现可能有助于开发皮肤健康和衰老控制的新疗法。

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