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培養(yǎng)基Sigma-Aldrich 干細胞培養(yǎng)

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  • 上海輔澤商貿(mào)有限公司
  • 2023-08-15 09:04:44
  • 上海市
  • Sigma-Aldrich
  • 1368

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【簡單介紹】

品牌 Sigma-Aldrich 貨號 干細胞
規(guī)格 神經(jīng)干細胞 供貨周期 一周
主要用途 間充質(zhì)干細胞 應用領(lǐng)域 化工
癌癥干細胞假說
癌癥干細胞概述
癌癥干細胞鑒定
癌癥干細胞信號轉(zhuǎn)導通路
干細胞培養(yǎng)實驗方案

【詳細說明】

癌癥干細胞假說

傳統(tǒng)觀點認為,癌癥是環(huán)境或內(nèi)部因素誘導正常細胞內(nèi)的關(guān)鍵致癌基因和腫瘤抑制基因突變導致的一種疾病。當這些突變導致細胞向更原始、高度增殖狀態(tài)轉(zhuǎn)化,克隆擴張形成白血病或?qū)嶓w腫瘤時,就會出現(xiàn)癌癥的臨床表現(xiàn)1。然而,這種模式不能夠*解釋許多腫瘤和轉(zhuǎn)移瘤的長發(fā)育延遲,產(chǎn)生細胞去分化和細胞永生的起始誘導機制,或腫瘤本身內(nèi)的細胞功能和表型多樣性起源。過去十年中,越來越多的證據(jù)表明,惡性腫瘤起源于組織干細胞在突變作用下的轉(zhuǎn)化,這些突變會導致控制干細胞生長和增殖的正常機制的調(diào)節(jié)異常1-9。

成體干細胞填充每個器官內(nèi)的離散區(qū)位。它們具有長生命期和多能性能,可以重新轉(zhuǎn)化成該器官內(nèi)的所有類型的細胞。干細胞的兩個顯著特性是:

  1. 在長期的區(qū)位環(huán)境中保持休眠的能力,

  2. 不對稱細胞分裂能力,可分裂為一個干細胞(稱作自我更新)和一個分化的子代。

支持CSC假說的例證

支持CSC假說的例證

此外,干細胞具有細胞凋亡耐受性,具有增強的端粒酶和DNA修復活性,并且具有膜結(jié)合的ABC轉(zhuǎn)運蛋白,能夠排除異物,從而使干細胞相對耐受劑和其他外源性毒物的損傷作用9-11 。自我更新加上長休眠期,使接觸損傷劑的干細胞能積聚可能隨著時間推移導致惡性轉(zhuǎn)化的突變3。


癌癥干細胞鑒定

研究人員已經(jīng)從大多數(shù)白血病2,4,13以及許多實體瘤(如腦膠質(zhì)母細胞瘤和成神經(jīng)管細胞瘤4,5,10,14,15 、乳腺3,16 、子宮頸、結(jié)腸直腸17,18 、胃腸道、肝細胞、肺、胰腺、前列腺和皮膚癌6,9,19,20)中分離得到少量的干細胞樣細胞。癌癥干細胞與其對應的正常干細胞具有相同的細胞表面標記物(見表1),但卻表現(xiàn)出不受控制的增殖,這可能是由于對負生長調(diào)節(jié)因子或?qū)佑|抑制和間隙連接細胞間通訊(GJIC)缺失的響應性降低所致。1,10


產(chǎn)品特點

AldeRed ALDH檢測分析

癌癥干細胞醛脫氫酶(ALDH)的表達量升高,被認為是所有CSCs的標志。ALDEFLUOR™檢測試劑盒過去一直用于測量ALDH的表達水平,并廣泛用于研究罕見的CSC群體。ALDEFLUOR檢測試劑盒的發(fā)射波長位于電磁光譜的綠色區(qū)域(512nm)。因此,其中的試劑不能同時用于表達綠色熒光蛋白(發(fā)射綠色熒光光譜)的細胞或小鼠。AldeRed是用于標記活ALDH陽性細胞的ALDH紅移熒光底物,從而釋放出綠色發(fā)射通道以幫助同步完成其他檢測。AldeRed克服了ALDEFLUOR檢測試劑盒目前的局限。

閱讀《Nature》中關(guān)于AldeRed的文章

AldeRed的特性和優(yōu)點:

  • 紅移檢測釋放出其他實驗所需的綠色通道

  • 活體干細胞鑒定技術(shù),能夠?qū)币姷募毎后w進行流式分選

  • 快速酶反應檢測方案

Aldered detection

Deab

AldeRed 588-A是一種無毒的ALDH熒光底物,能夠自由進入完整活細胞但其被ALDH轉(zhuǎn)化成酸產(chǎn)物后仍將滯留在細胞內(nèi)。

癌癥干細胞信號轉(zhuǎn)導通路

干細胞巢被充滿時,正常干細胞的自我更新將終止。與正常干細胞不同,癌癥干細胞和干細胞源癌祖細胞的不受控自我更新會超過其區(qū)位并滲入周圍組織13。Hedgehog,Notch,Wnt,和PTEN是控制正常和癌癥干細胞自我更新、增殖和存活的部分途徑。在大多數(shù)侵襲性癌癥中,都可觀察到導致這些途徑不同程度激活的突變。

Hedgehog 和 Bmi1通路

Hedgehog(Hh)通路能夠調(diào)節(jié)成體干細胞的休眠和自我更新。研究人員已經(jīng)在哺乳動物中鑒定了三種Hh配體,即Sonic hedgehog(Shh)、Desert hedgehog(Dhh)和Indian hedgehog(Ihh),其中對Shh的研究多。在沒有配體的情況下,Hh受體PTCH1通過催化抑制跨膜蛋白Smoothened(SMO),從而抑制信號轉(zhuǎn)導。配體與PTCH1可使受體失活,并活化SMO,繼而誘導Gli轉(zhuǎn)錄因子;Gli1和Gli2是Hh信號通路的陽性信號介導子,而Gli3是負調(diào)節(jié)子3,20。

Bmi1的誘導能夠促進許多Hh活化的效應。Bmi1 是一個的多梳基因,通過染色質(zhì)重塑抑制轉(zhuǎn)錄,并能夠下調(diào)Ink-4A / ADP核糖基化因子(ARF)復合物(如p16 Ink4A 和p19 ARF)的基因表達——這些基因是細胞周期的負調(diào)節(jié)物并且參與干細胞的休眠和分化3,4。這使得Hh通路元件PTCH1、Gli1和Gli2表達上調(diào)19,20, 以及Gli1和Gli2誘導的生長促進基因cyclin D1、Myc和Snail表達來實現(xiàn)干細胞分化和自我更新。

Notch-γ-分泌酶通路

Notch信號轉(zhuǎn)導能夠促進正常神經(jīng)干細胞的存活和增殖,抑制它們的分化。許多癌細胞系(包括T細胞白血病,以及腦、乳腺、卵巢、宮頸、結(jié)腸直腸、胰腺、唾液腺和肺部癌癥3,6,9,15 )的干細胞樣細胞中,Notch信號轉(zhuǎn)導通路被高度激活。其中,成神經(jīng)管細胞瘤和T細胞淋巴細胞白血病是Notch依賴性的惡性腫瘤15。

Notch通路激活包括通過γ-分泌酶對Notch配體/受體復合物進行蛋白水解切割,從而釋放Notch胞內(nèi)結(jié)構(gòu)域片段(NICD),移位到細胞核并上調(diào)Myc、Hes1和其他基因的表達。當用NICD2轉(zhuǎn)染DAOY成神經(jīng)管細胞瘤細胞系使Notch通路持續(xù)激活時,轉(zhuǎn)染后的細胞比非轉(zhuǎn)染的DAOY細胞產(chǎn)生更多的異種移植腫瘤,培養(yǎng)物中CD133 +和側(cè)群干細胞樣細胞也增加了。相反,抑制γ-分泌酶可將側(cè)群細胞減少至總細胞計數(shù)的0.01%,并且抑制90%的細胞形成軟瓊脂集落及在免疫受損的小鼠中形成腫瘤異種移植物的能力。NICD2轉(zhuǎn)染可保護細胞免受γ-分泌酶抑制的影響15。因此,在一些腫瘤類型中,抑制Notch信號轉(zhuǎn)導可以消除腫瘤起始所需的細胞群。

Wnt-β-連環(huán)蛋白途徑

Wnt包含結(jié)合Frizzled(Fz)受體家族的19種胞外糖蛋白家族,其可激活抑制β-連環(huán)蛋白的蛋白水解降解途徑,這使得β-連環(huán)蛋白在細胞質(zhì)中積累并向細胞核轉(zhuǎn)運。在細胞核中,β-連環(huán)蛋白通過Tcf / Lef轉(zhuǎn)錄因子促進基因轉(zhuǎn)錄。在Wnt未激活的情況下,軸蛋白(Axin)和腺瘤 息肉病大腸桿菌蛋白(APC)與糖原合酶激酶3(Gsk3)形成復合物,從而促進細胞質(zhì)β-連環(huán)蛋白磷酸化,繼而靶向β-連環(huán)蛋白以進行蛋白水解降解。

Wnt通路的激活需要Fz與其共同受體(LDL受體樣蛋白5/6(Lrp5 / 6))的結(jié)合。Wnt / Fz / Lrp5 / 6復合物的形成激活磷蛋白Dishevelled(Dvl)(Fz受體的組成成分),繼而招募Axin / Gsk3,從而解離Axin / APC / Gsk3復合物。Lrp5 / 6被Gsk3和酪蛋白激酶1γ(Ck1γ)。 磷酸化的Lrp5 / 6結(jié)合Axin / Gsk3形成復合體,防止β-連環(huán)蛋白的磷酸化從而穩(wěn)定β-連環(huán)蛋白。


癌癥干細胞中關(guān)鍵發(fā)育信號轉(zhuǎn)導通路的激活

圖1. 癌癥干細胞中關(guān)鍵發(fā)育信號轉(zhuǎn)導通路的激活。Shh、Wnt和Notch信號轉(zhuǎn)導途徑與維持癌癥干細胞的致瘤潛力有關(guān)。通過與Bmi1信號轉(zhuǎn)導介體和其他自我更新基因(如Nanog和Sox-2)的相互作用,這些新的調(diào)節(jié)機制可以促進或抑制自我更新,從而提供癌癥治療干預的方法。


材料






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    • 價格




    P9155聚-L-賴氨酸 氫溴酸鹽 mol wt 30,000-70,000, lyophilized powder, γ-irradiated, BioXtra, suitable for cell culture
    • 價格




    P6282聚-L-賴氨酸 氫溴酸鹽 mol wt 70,000-150,000, lyophilized powder, γ-irradiated, BioXtra, suitable for cell culture
    • 價格




    P5899聚-L-賴氨酸 氫溴酸鹽 mol wt ≥300,000, lyophilized powder, γ-irradiated, BioXtra, suitable for cell culture
    • 價格




    P4957聚-L-鳥氨酸 溶液 mol wt 30,000-70,000, 0.01%, sterile-filtered, BioReagent, suitable for cell culture
    • 價格




    C5533膠原 來源于人類胎盤 Bornstein and Traub Type IV, powder, BioReagent, suitable for cell culture
    • 價格




    C7661
    膠原 來源于大鼠尾 Bornstein and Traub Type I, powder, BioReagent, suitable for cell culture
    • 價格




    參考文獻

    1. Trosko, J.E., et al., Ignored hallmarks of carcinogenesis: stem cells and cell-cell communication. Ann. NY Acad. Sci., 1028, 192-201 (2004).

    2. Dick, J.E., Acute myeloid leukemia stem cells. Ann. NY Acad. Sci., 1044, 1-5 (2005).

    3. Liu, S., et al., Hedgehog signaling and Bmi-1 regulate self-renewal of normal and malignant human mammary stem cells. Cancer Res., 66, 6063-6071 (2006).

    4. Massard, C., et al., Tumor stem cell-targeted treatment: elimination or differentiation. Ann. Oncol., 17, 1620-1624 (2006).

    5. Meletis, K., et al., p53 suppresses the self-renewal of adult neural stem cells. Development, 133, 363-369 (2006).

    6. Mimeault, M., and Batra, S.K., Concise review: recent advances on the significance of stem cells in tissue regeneration and cancer therapies. Stem Cells, 24, 2319-2345 (2006).

    7. Shen, R., et al., Precancerous stem cells can serve as tumor vasculogenic progenitors. PLOS One, 3, e1652 (2008).

    8. Vermeulen, L., et al., Cancer stem cells - old concepts, new insights. Cell. Death Differ., e-pub Feb 15. 2008.

    9. Wicha, M.S., et al., Cancer stem cells: an old idea - a paradigm shift. Cancer Res., 66, 1883-1890 (2006).

    10. Sakariassen, P.O., et al., Cancer stem cells as mediators of treatment resistance in brain tumors: status and controversies. Neoplasia, 9, 882-892 (2007).

    11. Styczynski, J., and Drewa, T., Leukemic stem cells: from metabolic pathways and signaling to a new concept of drug resistance targeting. Acta Biochim. Pol., 54, 717-726 (2007).

    12. Bailey, P., and Cushing, H., A Classification of the Tumors of the Glioma Group on a Histogenetic Basis with a Correlated Study of Prognosis. Philadelphia: J.P. Lippincott, (1926).

    13. Strewler, G.J., The stem cell niche and bone metastasis. BoneKEy-Osteovision, 3, 19-29 (2006).

    14. Singh, S.K., et al. Identification of a cancer stem cell in human brain tumors. Cancer Res., 63, 5821-5828 (2003).

    15. Fan, X., et al., Notch pathway inhibition depletes stem-like cells and blocks engraftment in embryonal brain tumors. Cancer Res., 66, 7445-7452 (2006).

    16. Benhaj, K., et al., Redundant expression of canonical Wnt ligands in human breast cancer cell lines. Oncol. Rep., 15, 701-707 (2006).

    17. Fodde, R., and Brabletz, T., Wnt/β-catenin signaling in cancer stemness and malignant behavior. Curr. Opin. Cell Biol., 19, 150-158 (2007).

    18. Zhou, J., et al., Activation of the PTEN/mTOR/STAT3 pathway in breast cancer stemlike cells is required for viability and maintenance. Proc. Natl. Acad. Sci. USA, 104, 16158-16163 (2007).

    19. Mimeault, M., and Batra, S.K., Interplay of distinct growth factors during epithelialmesenchymal transition of cancer progenitor cells and molecular targeting as novel cancer therapies. Ann. Oncol., 18, 1605-1619 (2007).

    20. Peacock, C.D., et al., Hedgehog signaling maintains a tumor stem cell compartment in multiple myeloma. Proc. Natl. Acad. Sci. USA, 104, 4048-4053 (2007).

    21. Bao, S., et al., Stem cell-like glioma cells promote tumor angiogenesis through vascular endothelial growth factor. Cancer Res., 66, 7843-7848 (2006).

    22. O’Neil, J., et al., FBW7 mutations in leukemic cells mediate NOTCH pathway activation and resistance to γ-secretase inhibitors. J. Exp. Med., 204, 1813-1824 (2007).

    23. He, X., and Axelrod, J.D., A WNTer wonderland in Snowbird. Development, 133, 2597-2603 (2006).

    24. Zeng, X., et al., Initiation of Wnt signaling: control of Wnt coreceptor Lrp6 phosphorylation/activation via frizzled, disheveled and axin functions. Development, 135, 367-375 (2008).

    25. Groszer, M., et al., PTEN negatively regulates neural stem cell self-renewal by modulating G0-G1 cell cycle entry. Proc. Natl. Acad. Sci. USA,103, 111-116 (2006).

    26. Hede, K., PTEN takes center stage in cancer stem cell research, works as tumor suppressor. J. Nat. Cancer Inst., 98, 808-809 (2006).

    27. A red-shifted fluorescent substrate for aldehyde dehydrogenase. Martin G. Pomper et al. Nature Communications 5, Article number: 3662 23 April 2014

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