中國(guó)藥科大學(xué)用紫外交聯(lián)儀UCL-3500M構(gòu)建光損傷細(xì)胞模型

概要：中國(guó)藥科大學(xué)在《Cosmetics》發(fā)表文獻(xiàn)《Photoprotective Effect and Potential Mechanisms of Gardeniae Fructus Extract in UVB-HIrradiated HaCaT Cells》，文獻(xiàn)中使用紫外交聯(lián)儀UCL-3500M模擬UVB紫外線輻照，構(gòu)建HaCaT 細(xì)胞光損傷模型，對(duì)皮膚光損傷相關(guān)研究有重要參考意義。

在該細(xì)胞研究中，紫外交聯(lián)儀UCL-3500M通過(guò)模擬自然環(huán)境中UVB紫外線對(duì)皮膚的照射，定向誘導(dǎo) HaCaT 細(xì)胞產(chǎn)生與體內(nèi)光損傷高度相似的生理病理變化，為后續(xù)探究活性成分的作用機(jī)制、篩選高效光保護(hù)物質(zhì)提供了可靠的實(shí)驗(yàn)載體。

紫外交聯(lián)儀 UCL-3500M的優(yōu)勢(shì)

優(yōu)勢(shì)一：紫外交聯(lián)儀UCL-3500M可以提供定時(shí)或定量的UVB紫外線輻照，劑量精準(zhǔn)且UVB光照均勻穩(wěn)定，非常適合構(gòu)建各類紫外光損傷細(xì)胞模型。

優(yōu)勢(shì)二：紫外交聯(lián)儀UCL-3500M滿足紫外光損傷模型的光譜要求。UCL-3500M的波長(zhǎng)與自然環(huán)境中到達(dá)地球表面的 UVB（290-320nm）波段契合，因此可以真實(shí)模擬皮膚暴露于日光時(shí)的UVB照射條件，模擬UVB誘導(dǎo)的皮膚細(xì)胞損傷特征。

優(yōu)勢(shì)三：紫外交聯(lián)儀UCL-3500M使用專為輻照細(xì)胞設(shè)計(jì)的溫控系統(tǒng)，無(wú)需擔(dān)心溫度過(guò)高損傷細(xì)胞。

紫外交聯(lián)儀UCL-3500M劑量精準(zhǔn)、操作簡(jiǎn)單、光照均勻，廣泛用于國(guó)內(nèi)外高校和科研院所，進(jìn)行紫外光損傷細(xì)胞模型的構(gòu)建。設(shè)備可選擇時(shí)間模式，能量模式，預(yù)設(shè)模式等多種方式操作。另外，紫外交聯(lián)儀UCL-3500系列還有254nm、365nm等多種波長(zhǎng)可選，可以滿足不同細(xì)胞實(shí)驗(yàn)的要求。

原文段落:

Abstract: Gardeniae Fructus (GF), the desiccative mature fruitage of Gardenia jasminoides J. Ellis (G. jasminoides), is a traditional herbal medicine in China with potential value against skin photodamage. However, the phytochemical basis and mechanisms underlying GF’s anti-photodamage effects remain unclear. In this study, the chemical components in GF extract (GFE) were analyzed using ultra-high-performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS), and iridoids were identified as the main components. The antioxidant, anti-inflammatory, and barrier-repair effects of GFE in UVB-induced photodamage were assessed through in vitro experiments. Additionally, the potential mechanisms of GFE against skin photodamage were predicted using proteomics and network pharmacology. The results showed that GFE significantly increased the levels of total superoxide dismutase (T-SOD), catalase (CAT), and glutathione peroxidase (GSH-Px) induced by UVB, while decreasing reactive oxygen species (ROS) and malondialdehyde (MDA) contents. GFE also inhibited the secretion of interleukin-6 (IL-6) and interleukin-1β (IL-1β). Additionally, GFE upregulated the expression of filaggrin (FLG), loricrin (LOR), and involucrin (IVL) in 3D epidermal skin models. Proteomic analysis and network pharmacology indicated that the iridoid components identified in GFE ameliorated UVB-induced damage probably by regulating cell cycle-related proteins and signaling pathways, though this requires further experimental confirmation. Overall, the results provide essential evidence to support the development of GFE as a skincare active ingredient.

UV crosslinker (Luyor, Shanghai, China) UVB lamps (302 nm) were applied for cell modeling at 10 mJ/cm2. The HaCaT cells had a thin film of phosphate-buffered saline (PBS) on them and were irradiated by UVB. After irradiation, the medium was replaced with fresh medium and incubated for 24 h.

原文獻(xiàn)下載地址：//doi.org/10.3390/cosmetics12020072