中文摘要：

白斑?。?span style="font-family: PingFangSC, PingFangSC-Regular; font-size: 16px; text-align: justify; background-color: rgb(255, 255, 255);">Vitiligo）是一種由皮膚黑素細(xì)胞缺失引起的自身免疫性皮膚病。雖然光療和T細(xì)胞抑制療法已被廣泛用于誘導(dǎo)表皮色素再生，但由于人們對(duì)這一過(guò)程的細(xì)胞和分子調(diào)控機(jī)制理解不足，很少能實(shí)現(xiàn)色素恢復(fù)。本研究發(fā)現(xiàn)，雌雄小鼠黑色素干細(xì)胞（McSC）的表皮遷移速率存在顯著差異，這種差異源于紫外線B照射引發(fā)的性別二態(tài)性皮膚炎癥反應(yīng)。通過(guò)使用基因工程小鼠模型及無(wú)偏倚的批量mRNA測(cè)序與單細(xì)胞mRNA測(cè)序技術(shù)，我們證實(shí)通過(guò)調(diào)控環(huán)氧合酶及其下游前列腺素產(chǎn)物的炎癥反應(yīng)，可以有效調(diào)節(jié)紫外線B暴露下黑色素干細(xì)胞的增殖和表皮遷移。進(jìn)一步研究表明，通過(guò)聯(lián)合調(diào)控巨噬細(xì)胞和T細(xì)胞（即先天免疫和適應(yīng)性免疫）的療法可顯著促進(jìn)表皮黑素細(xì)胞再生?；谶@些發(fā)現(xiàn)，我們提出了一種針對(duì)Vitiligo等色素脫失性疾病患者的新型復(fù)色治療策略。

英文摘要：

Vitiligo is an autoimmune skin disease caused by cutaneous melanocyte loss. Although phototherapy and T cell suppression therapy have been widely used to induce epidermal re-pigmentation, full pigmentation recovery is rarely achieved due to our poor understanding of the cellular and molecular mechanisms governing this process. Here, we identify unique melanocyte stem cell (McSC) epidermal migration rates between male and female mice, which is due to sexually dimorphic cutaneous inflammatory responses generated by ultra-violet B exposure. Using genetically engineered mouse models, and unbiased bulk and single-cell mRNA sequencing approaches, we determine that manipulating the inflammatory response through cyclooxygenase and its downstream prostaglandin product regulates McSC proliferation and epidermal migration in response to UVB exposure. Furthermore, we demonstrate that a combinational therapy that manipulates both macrophages and T cells (or innate and adaptive immunity) significantly promotes epidermal melanocyte re-population. With these findings, we propose a novel therapeutic strategy for repigmentation in patients with depigmentation conditions such as vitiligo.

論文信息：

論文題目：Sexual dimorphism in melanocyte stem cell behavior reveals combinational therapeutic strategies for

cutaneous repigmentation

期刊名稱：Nature Communications

時(shí)間期卷：15, Article number: 796 (2024)

在線時(shí)間：2024年1月27日

DOI：doi.org/10.1038/s41467-024-45034-3

產(chǎn)品信息：

貨號(hào)：CP-005-005

規(guī)格：5ml+5ml

品牌：Liposoma

產(chǎn)地：荷蘭

名稱：Clodronate Liposomes and Control Liposomes

辦事處：Target Technology（靶點(diǎn)科技）

白斑病是由于皮膚黑素細(xì)胞被破壞，引發(fā)皮膚黑色素缺乏，形成局部白斑的疾病。其病因可能與自身免疫系統(tǒng)疾病、遺傳、神經(jīng)化學(xué)物質(zhì)等因素有關(guān)，不同年齡、性別和種族的人都可能患病。皮膚色素障礙疾病種類繁多。白斑病作為一種典型的自身免疫性疾病，全球發(fā)病率達(dá)0.5%-2%，其特征表現(xiàn)為表皮黑素細(xì)胞缺失導(dǎo)致的色素脫失斑塊。

白斑病發(fā)病機(jī)制涉及遺傳易感性、氧化應(yīng)激、先天/適應(yīng)性免疫異常及環(huán)境刺激等多重因素，這些因素共同導(dǎo)致CD8?T細(xì)胞異?；罨罱K引發(fā)表皮黑素細(xì)胞破壞。因此，針對(duì)T細(xì)胞的靶向治療成為研究焦點(diǎn)。近期FDA批準(zhǔn)的多種JAK抑制劑通過(guò)抑制CD8?T細(xì)胞募集，在改善白斑病患者復(fù)色方面顯示出療效。盡管II/III期臨床試驗(yàn)證實(shí)這些療法可顯著改善皮膚色素沉著，但患者應(yīng)答存在個(gè)體差異，且鮮有實(shí)現(xiàn)持久的色素再生。

氯膦酸鹽二鈉脂質(zhì)體清除單核巨噬細(xì)胞，在白斑病模型中單核巨噬細(xì)胞功能研究，荷蘭Liposoma巨噬細(xì)胞清除劑Clodronate Liposomes見(jiàn)刊于Nature Communications：

Liposoma巨噬細(xì)胞清除劑Clodronate Liposomes氯膦酸二鈉脂質(zhì)體的材料和方法：

Clodronate liposome treatment

Mice were given doxycycline in water and the first dose of clodronate liposomes (CL) or PBS liposomes (PL) (Liposoma, Cat#CP-005-005) on the day prior to the first UVB irradiation. Male and female mice were given 250?µl and 200?µl CL/PL, respectively, due to weight differences. From one day after the first UVB, mice were given CL/PL daily until the collection day or 2 days following the third UVB. Mice for McSC translocation analysis were collected seven days following the third UVB irradiation.