Rosiglitazone(BRL 49653,AbMole,M1894)是一種噻唑烷二酮類化合物,Rosiglitazone作為過氧化物酶體增殖物激活受體γ(PPARγ)的高親和力激動(dòng)劑在科研中備受關(guān)注。PPARγ是核受體超家族中的一名關(guān)鍵成員,其本質(zhì)上是一個(gè)依賴配體激活的轉(zhuǎn)錄因子,它在調(diào)控基因表達(dá)(尤其是涉及能量代謝和細(xì)胞分化的基因)方面起到重要的調(diào)節(jié)作用。而Rosiglitazone可直接結(jié)合PPARγ配體結(jié)合域,通過調(diào)控下游靶基因的表達(dá)發(fā)揮生物學(xué)效應(yīng)
[1, 2]。在分子層面,Rosiglitazone(CAS No.:122320-73-4)可調(diào)節(jié)NF-κB等炎癥信號(hào),以及葡萄糖轉(zhuǎn)運(yùn)和脂肪合成等代謝相關(guān)的通路。例如Rosiglitazone可降低p65磷酸化水平并上調(diào)IκBα表達(dá),這種抗炎作用在PPARγ被敲除后消失,證實(shí)其核心機(jī)制依賴于PPARγ的激活。此外,最新發(fā)現(xiàn)Rosiglitazone還能作為視黃醇X受體α(RXRα)的配體,通過RXRα依賴性途徑調(diào)控基因轉(zhuǎn)錄
[3]。在細(xì)胞實(shí)驗(yàn)中,Rosiglitazone(BRL 49653)表現(xiàn)出多效性:(1)抑制細(xì)胞增殖,Rosiglitazone可通過劑量和時(shí)間依賴性的方式阻滯細(xì)胞周期并誘導(dǎo)凋亡,顯著降低5637細(xì)胞和T24細(xì)胞的遷移能力
[4];(2)調(diào)節(jié)線粒體功能,Rosiglitazone可保護(hù)線粒體,促進(jìn)線粒體中的氧化磷酸化,增加細(xì)胞內(nèi)ATP的水平,該作用可被PPARγ拮抗劑
GW9662(AbMole,M2748)逆轉(zhuǎn)
[5];(3)調(diào)控巨噬細(xì)胞極化,Rosiglitazone可抑制M1型巨噬細(xì)胞但促進(jìn)M2型巨噬細(xì)胞的極化,以及促進(jìn)小膠質(zhì)細(xì)胞的吞噬功能,這種增強(qiáng)作用與PPARγ/CD36軸激活密切相關(guān)
[6];(4)誘導(dǎo)細(xì)胞分化:在脂肪細(xì)胞分化實(shí)驗(yàn)中,Rosiglitazone可顯著促進(jìn)3T3-L1前脂肪細(xì)胞的脂質(zhì)積累并分化為脂肪細(xì)胞
[7]。在動(dòng)物實(shí)驗(yàn)中,Rosiglitazone能減輕小鼠腦出血模型的神經(jīng)損傷,通過PPARγ/JNK/STAT3軸抑制細(xì)胞凋亡
[8]。Rosiglitazone在小鼠肺纖維化模型中,可通過抑制p38 MAPK磷酸化緩解纖維化進(jìn)程
[9]。
AbMole為全球科研客戶提供高純度、高生物活性的抑制劑、細(xì)胞因子、人源單抗、天然產(chǎn)物、熒光染料、多肽、靶點(diǎn)蛋白、化合物庫(kù)、抗生素等科研試劑,全球大量文獻(xiàn)專利引用。
范例詳解
Adv Sci (Weinh). 2023 May;10(15):e2207224.
重慶醫(yī)科大學(xué)的實(shí)驗(yàn)人員在上述論文中探討了缺氧如何通過調(diào)控巨噬細(xì)胞極化和破骨細(xì)胞生成,驅(qū)動(dòng)骨修復(fù)材料誘導(dǎo)的異位骨形成(heterotopic ossification, HO)。核心發(fā)現(xiàn)是:缺氧環(huán)境通過激活缺氧誘導(dǎo)因子-1α(HIF-1α),促進(jìn)巨噬細(xì)胞向M2型極化并積累脂質(zhì),進(jìn)而融合形成破骨細(xì)胞;而破骨細(xì)胞分泌的因子(如CTHRC1、S1P)可進(jìn)一步誘導(dǎo)間充質(zhì)干細(xì)胞的成骨分化,最終導(dǎo)致異位骨形成。這一機(jī)制為骨修復(fù)材料的設(shè)計(jì)提供了新思路。Rosiglitazone(BRL 49653,AbMole,M1894)作為M2型巨噬細(xì)胞激活劑,在本文中起到了陽性對(duì)照的作用,以證實(shí)巨噬細(xì)胞極化在上述模型中的作用。
2014年,AbMole的兩款抑制劑分別被西班牙國(guó)家心血管研究中心和美國(guó)哥倫比亞大學(xué)用于動(dòng)物體內(nèi)實(shí)驗(yàn),相關(guān)科研成果發(fā)表于頂刊 Nature 和 Nature Medicine。

Cilengitide partially inhibited rosiglitazone-induced M2 polarization.
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參考文獻(xiàn)及鳴謝
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[4] X. Xu, J. Wang, H. Jiang, et al., Rosiglitazone induces apoptosis on human bladder cancer 5637 and T24 cell lines, International journal of clinical and experimental pathology 10(10) (2017) 10197-10204.
[5] J. M. Ortiz-Rodriguez, C. Balao da Silva, J. Masot, et al., Rosiglitazone in the thawing medium improves mitochondrial function in stallion spermatozoa through regulating Akt phosphorylation and reduction of caspase 3, PloS one 14(7) (2019) e0211994.
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