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本研究拟通过小分子化合物氯化钴(CoCl2)模拟的低氧环境,探讨雷帕霉素(RPM)对该低氧下人急性髓细胞白血病HL-60细胞的生物学行为的影响。低氧模拟组、低氧雷帕霉素处理组、常氧雷帕霉素处理组HL-60细胞分别采用CoCl2、CoCl2/RPM、RPM进行处理,对照组为常氧下常规培养的HL-60细胞,处理及培养24h、48h、72h后收集细胞,采用倒置相差显微镜观察细胞生长状况,常规瑞氏染色后光学显微镜下观察细胞形态;MTT比色法检测各组细胞的活性和增殖能力;AnnexinV—FITC/PI双染法流式细胞术检测细胞凋亡。结果表明,与对照组细胞形态规则,胞核呈圆形或椭圆形相比,低氧模拟组和低氧雷帕霉素处理组细胞密度降低,生长明显受抑,细胞胞核呈不规则形或杆状,染色质粗糙,伴扭曲折叠等变化。各组间不同时问细胞增殖抑制率差异显著(P〈0.05),低氧模拟组和低氧雷帕霉素处理组增殖抑制率随着处理时间延长而增大,且低氧雷帕霉素处理组的增殖抑制率大于低氧模拟组。与常氧下的对照组及雷帕霉素处理组比较,低氧的模拟组和雷帕霉素处理组诱导细胞发生较明显的凋亡,且后期72h低氧雷帕霉素处理组凋亡率显著高于模拟低氧处理组。以上结果表明,模拟低氧环境下,HL-60细胞生长明显受抑制,且诱导细胞凋亡;雷帕霉素可增强对低氧对细胞的生长抑制和诱导凋亡作用。 相似文献
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目的:探讨骨髓间充质干细胞(MSCs)移植对大鼠低氧性肺动脉高压(HPH)的影响。方法:体外分离、培养、鉴定SD大鼠骨髓MSCs、绿色荧光蛋白腺病毒标记MSCs细胞。将健康雄性SD大鼠随机分为4组:正常对照组(NC组)8只、低氧性肺动脉高压组(HPH组)8只,低氧性肺动脉高压同时骨髓间充质干细胞移植组(MSCs组)24只,低氧性肺动脉高压同时携带血管内皮生长因子(VEGF)的MSCs移植组(VEGF+MSCs组)24只。采用常压间歇低氧法建立大鼠肺动脉高压模型,干细胞转染并行干细胞移植。观察大鼠平均肺动脉压力(mPAP),计算右心室肥厚指数(RVHI),显微镜下观察各组大鼠肺小动脉形态结构改变,并在荧光显微镜下观察干细胞移植7d,14d,28d时腺病毒转染荧光标记的MSCs在肺小动脉分布及表现。结果:NC组28d时mPAP(mmHg)为15.5±1.5,而HPH组、MSCs组及MSCs+VEGF组分另q为26.1±1.9、21.6±2.7及20.1±2.9,均明显高于NC组(P〈0.01),但MSCs组及MSCs+VEGF组较HPH组明显下降(P〈0.01),MSCs组与MSCs+VEGF组无明显差别。NC组28d时RVHI为0.28±0.02,而HPH组、MSCs组及MSCs+VEGF组RVHI分别为0.43±0.07、0.34±0.03及0.35±0.01,均明显高于NC组(P〈0.01),但MSCs组及MSCs+VEGF组较HPH组明显下降(P〈0.05),MSCs组与MSCs+VEGF组无明显差别。HPH组28d时,肺小动脉管壁明显增厚,管腔明显狭窄、闭塞,内皮细胞不完整,而MSCs组血管壁较HPH组变薄,管腔通畅,内皮细胞完整性改善,MSC8组及MSCs+VEGF组的表现改变不明显。结论:骨髓间充质干细胞移植可改善肺小动脉血管重塑,从而部分逆转HPH的进程;而将VEGF与MSCs联合移植并未提高单纯MSCs移植的作用。 相似文献
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摘要目的:通过小分子化合物氯(CoCt2)模拟的低氧环境,分析低氧下及其雷帕霉素(RPM)作用下人急性髓细胞白血病细胞HL.60的低氧调控信号分子表达的变化;方法:常规方法复苏、传代、培养HL-60细胞,培养细胞进入对数生长期后用于实验。低氧模拟组、低氧雷帕霉素处理组、常氧雷帕霉素处理组分别用含2001xmol/LCoCl2、2001xmol/LCOCl2/20nmol/LRPM、20nmol/LRPM的1640培养基处理生长状态良好的细胞,对照组细胞用1640培养基培养,各组置培养箱以37℃、5%CO2培养,并于处理后24h、48h、72h收集细胞用于检测;采用实时荧光定量PCR方法检测低氧诱导因子(HIF-1α)、内皮细胞生长因于(VEGF)、雷帕霉素靶蛋白(mTOR)及GAPDH在转录水平的表达;结果:①与各时段对照组相比,低氧模拟组HIF-1α表达随时间逐渐增加,72h明显上调;与常氧雷帕霉素处理组各时段比较,低氧雷帕霉素处理组HIF-1α表达早期(24h)相对下调,后期相对上调;②.与对照组比较,各处理组mTOR表达均下调,低氧雷帕霉素处理组在早期(24h)下调显著;与常氧雷帕霉素处理组比较,低氧雷帕霉素处理组mTOR各时段的表达均相对下调;③与对照组各时段相比,低氧模拟组VEGF的表达在早期显著上调,但后期呈下调;常氧雷帕霉素处理组各时段VEGF的表达下调,与其比较,低氧雷帕霉素处理组各时段均呈相对下调。结论:常氧和低氧下RPM作用HL-60细胞后VEGF、mTOR的mRNA均表达下调,RPM可在低氧环境下增强了这种下调表达作用。 相似文献
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Akt基因转染对骨髓间充质干细胞缺氧时凋亡和增殖的影响 总被引:3,自引:0,他引:3
目的采用Akt基因转染鼠骨髓MSCs探讨Akt基因是否减轻MSCs缺氧时的凋亡和提高缺氧时的增殖能力,即耐缺氧能力。方法将转染和未转染Akt基因的MSCs置于94%N2、1%O2和5%CO2缺氧箱中37℃孵育不同时间(常氧、缺氧0.5h、1h、2h、4h和8h)后,Annexin V/PI双染法行流式细胞仪分析凋亡率(apoptoticrate,AR)和死亡率(deadrate,DR)、MTT法分析细胞增殖状态、Rt-PCR和Western blot等检测Akt和p-Akt表达以及放射同位素法检测MSCs对氚标-葡萄糖(^3H-G)的摄取等。结果1.Akt基因显著降低MSCs缺氧时AR和DR(P〈0.01),而各缺氧时间点没有统计学意义(P〉0.05);2.Akt基因显著增高MSCs常氧和缺氧(与未转染Akt基因MSCs同等条件下比较)时增殖能力(P〈0.01),缺氧时增殖能力显著低于常氧时(P〈0.01);3.Akt基因显著增高常氧时MSCsAkt mRNA(P〈0.01)和蛋白(P〈0.01)表达,而不增高p-Akt蛋白(P〉0.05)表达;Akt基因显著提高缺氧时p-Akt蛋白(P〈0.01)表达,而不提高常氧时p-Akt蛋白(P〉0.05)表达;4.Akt基因显著增高MSCs常氧和缺氧(与未转染Akt基因MSCs同等条件下比较)时^3H-G的摄取(P〈0.01),缺氧时^3H-G的摄取显著性低于常氧培养时(P〈0.01);^3H-G的摄取与细胞增殖显著正相关(r=0.79,P=0.015)而与细胞凋亡显著负相关(r=-1.47,P=0.023)。结论Akt基因转染可显著提高MSCs耐缺氧能力,此可能与缺氧时改善MSCs葡萄糖摄取等有关。 相似文献
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间充质干细胞(mesenchymal stemcells, MSCs)是具有自我更新、多向分化和强可塑性的细胞,具有分化为血液、骨、软骨、脂肪、肌肉、表皮、上皮、神经等组织的潜能,受到再生医学研究的关注。目前已有研究表明将MSCs 移植到多种损伤组织中都能改善损伤组织的功能。文章在简要回顾了低氧环境对MSCs增殖和分化的研究内容和有关理论争论基础上重点介绍了缺氧诱导因子(HIF)通路对MSCs 增殖和分化的影响。文章阐述了低氧环境对MSCs向成骨,成软骨,成脂及成神经元方向分化的影响。由于人体组织内生理条件下的氧张力远远小于大气中的氧张力(21%),采用低氧培养MSCs 的研究方法得出的结论将更加贴近实际MSCs在人体内的增殖、分化情况。因此研究MSCs 在低氧张力环境中增殖、分化的能力将为MSCs 能成功移植到体内并发挥作用提供保障。 相似文献
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目的:观察低氧对间充质干细胞(MSC)成骨相关基因表达的影响。方法:取第2代MSC,分别在常氧和3%氧浓度下培养,采用real-timeRT-PCR检测骨桥蛋白(OPN)、核心结合因子α1(Cbfal)、骨形态发生蛋白(BMP)和血管内皮生长因子(VEGF)mRNA的表达。结果:2种氧浓度下MSC的形态无明显差异,但3%氧浓度下MSC集落形成能力增强。常氧下MSC中Cbfal和BMPmRNA的表达高于3%氧浓度,差异有显著性(P〈0.05);而OPN和VEGFmRNA的表达虽高于3%氧浓度,但差异无显著性(P〉0.05)。结论:3%氧浓度对MSC的形态没有明显影响,但增强其增殖能力,抑制其成骨分化能力。 相似文献
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低氧促进神经干细胞向多巴胺能神经元分化 总被引:2,自引:0,他引:2
神经干细胞(neural stem cells,NSCs)作为具有多向分化潜能的神经前体细胞,被广泛应用于细胞移植等研究,而低氧不但调节干细胞的体外增殖,在干细胞分化中也具有重要的作用。本文着重探讨了低氧对NSCs分化的调节作用。采用Wistar孕大鼠(E13.5d),分离胚胎中脑NSCs,加入无血清DMEM/F12培养液(含20ng/mL EGF、20ng/mL bFGF、1% N2和B27),3~5d后传代,细胞培养至第三代进行诱导分化,分别在低氧(3%O2)和常氧(20%O2)条件下诱导分化3d,然后在常氧条件下分化成熟5~7d(DMEM/F12含1%FBS、N2和B27)后进行检测。Nestin、NeuN以及TH免疫组织化学鉴定NSCs;流式细胞术分析测定NSCs向TH阳性神经元方向的分化;高效液相色谱测定细胞培养上清液中多巴胺(dopamine,DA)含量。结果显示,分离培养的NSCs均为nestin阳性细胞;低氧可明显促进NSCs向神经元方向的分化;TH阳性神经元比例在常氧和低氧组分别为(10.25±1.03)%和(19.88±1.44)%。NSCs诱导分化7d后,低氧组细胞培养上清液中DA浓度明显增加,约为常氧组的2倍(P〈0.05,n=8)。上述结果表明,3%低氧可促进NSCs向神经元方向,特别是向DA能神经元方向分化。这为NSCs应用于临床治疗帕金森病提供了基础。 相似文献
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低氧条件下大鼠肺动脉平滑肌细胞中活性氧与低氧诱导因子-1α和细胞增殖的关系 总被引:2,自引:0,他引:2
在低氧条件下,观察大鼠肺动脉平滑肌细胞(pulmonary arterial smooth muscle cells,PASMCs)中活性氧(reactive oxygen species,ROS)的变化,探讨ROS的变化是否通过调控低氧诱导因子-4α(hypoxia-inducible factor 1α, HIF-1α)的表达影响PASMCs的增殖。采用组织块法原代培养大鼠PASMCs,分成3组:常氧组(21%O2,24h),低氧组(5%O2,24h),低氧+Mn-TBAP组(5%O2,24h,Mn-TBAP是一种ROS清除剂)。用激光共聚焦显微镜荧光染色法检测细胞内ROS的变化;用RT-PCR和免疫组织化学方法分别测定HIF-1α mRNA和蛋白的表达;用MTT法检测细胞增殖程度。结果显示:(1)低氧组PASMCs内ROS水平明显高于常氧组(P〈0.05),低氧+Mn-TBAP组ROS水平明显低于低氧组(P〈0.05),但仍高于常氧组(P〈0.05);(2)低氧组及低氧+Mn-TBAP组的HIF-1α mRNA和蛋白表达均高于常氧组(P〈0.05),且低氧组表达高于低氧+Mn-TBAP组(P〈0.05);(3)低氧组细胞增殖明显高于常氧组和低氧+Mn-TBAP组(P〈0.05),低氧+Mn-TBAP组细胞增殖高于常氧组(P〈0.05)。结果表明:在低氧条件下大鼠PASMCs中ROS水平明显升高,RROS的变化能够调节HIF-1α的表达,进而影响平滑肌细胞的增殖,提示ROS可能在肺动脉高压的发病机制和低氧信号转导中具有重要作用。 相似文献
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摘要: 间充质干细胞(mesenchymal stem cells, MSCs)是具有自我更新、 多向分化和强可塑性的细胞, 具有分化为血液、 骨、 软骨、 脂
肪、 肌肉、 表皮、 上皮、 神经等组织的潜能, 受到再生医学研究的关注。目前已有研究表明将 MSCs 移植到多种损伤组织中都能改
善损伤组织的功能。文章在简要回顾了低氧环境对 MSCs 增殖和分化的研究内容和有关理论争论基础上重点介绍了缺氧诱导因
子 ( HIF )通路对 MSCs 增殖和分化的影响。文章阐述了低氧环境对 MSCs 向成骨,成软骨,成脂及成神经元方向分化的影响。 由于
人体组织内生理条件下的氧张力远远小于大气中的氧张力 (21% ), 采用低氧培养 MSCs 的研究方法得出的结论将更加贴近实际
MSCs 在人体内的增殖、分化情况。因此研究 MSCs 在低氧张力环境中增殖、分化的能力将为 MSCs 能成功移植到体内并发挥作
用提供保障。 相似文献
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该研究体外分离山羊颞下颌关节盘(temporomandibular joint disc,TMJ disc)细胞并培养至p2代。通过HE(Hematoxylin-Eosin)染色、Hoechst 33258和丹磺酰戊二胺(dansylcadaverine,MDC)荧光染色观察血清剥夺后细胞的形态学变化以及是否存在自噬和凋亡。随后,通过流式细胞术和实时荧光定量聚合酶链反应(Real-time PCR)分别检测血清剥夺0 h、12 h、24 h、36 h、48 h和60 h后细胞的凋亡率和自噬水平的变化以及加入自噬抑制剂3-MA(3-methyladenine)后的凋亡变化。检测给予血清(10%FBS)或血清剥夺(0%FBS)的细胞在常氧(21%O2)或低氧(2%O2)条件下的凋亡和自噬的变化。结果发现:血清剥夺后,凋亡率随时间的延长逐渐上升,自噬率先上升后下降;当血清剥夺诱导的自噬被3-MA抑制后,细胞的凋亡率明显上升。自噬能够抑制血清剥夺引起的细胞凋亡,说明自噬在细胞的存活中有很重要的作用。与常氧培养的细胞相比,低氧条件下细胞的凋亡率和自噬率均下降。低氧通过降低细胞的过度自噬减少长期血清剥夺引起的细胞凋亡,比常氧更有利于细胞的存活。 相似文献
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Nadri S Soleimani M Kiani J Atashi A Izadpanah R 《Differentiation; research in biological diversity》2008,76(3):223-231
Abstract Identification of mesenchymal stem cells (MSCs) derived from alternative sources has provided an exciting prospect for intensive investigation. This work focused on characterizing a new source of MSCs from stromal cells from human eye conjunctiva. In this study, after conjunctiva biopsies and culture of stromal segment of this tissue, fibroblast-like (SH2+ , SH3+ , CD29+ , CD44+ , CD166+ , CD13+ ) human stromal cells, which can be differentiated toward the osteogenic, adipogenic, chondrogenic, and neurogenic lineages, were obtained. These cells expressed Oct-4, Nanog, Rex-1 genes, and some lineage-specific markers like cardiac actin and Keratin. Taken together, the results indicate that conjunctiva stromal-derived cells are a new source of multipotent MSCs and despite originating from an adult source, they express undifferentiated stem cell markers. 相似文献
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Nadja Zeltner Fabien G. Lafaille Faranak Fattahi Lorenz Studer 《Journal of visualized experiments : JoVE》2014,(87)
Human pluripotent stem cells (hPSCs) have great potential for studying human embryonic development, for modeling human diseases in the dish and as a source of transplantable cells for regenerative applications after disease or accidents. Neural crest (NC) cells are the precursors for a large variety of adult somatic cells, such as cells from the peripheral nervous system and glia, melanocytes and mesenchymal cells. They are a valuable source of cells to study aspects of human embryonic development, including cell fate specification and migration. Further differentiation of NC progenitor cells into terminally differentiated cell types offers the possibility to model human diseases in vitro, investigate disease mechanisms and generate cells for regenerative medicine. This article presents the adaptation of a currently available in vitro differentiation protocol for the derivation of NC cells from hPSCs. This new protocol requires 18 days of differentiation, is feeder-free, easily scalable and highly reproducible among human embryonic stem cell (hESC) lines as well as human induced pluripotent stem cell (hiPSC) lines. Both old and new protocols yield NC cells of equal identity. 相似文献
15.
目的寻找可以维持人胚胎干细胞未分化生长的人源性细胞作为饲养层细胞,从而解决使用鼠源性细胞作为饲养层带来的安全问题。方法尝试以人脐带间充质干细胞作为饲养层细胞来培养人胚胎干细胞,检验其是否可以维持人胚胎干细胞的未分化生长状态。用胶原酶消化法分离人脐带间充质干细胞,光镜下观察细胞形态;流式细胞仪检测其表面标志;诱导人脐带间充质干细胞向成骨细胞和脂肪细胞进行分化。将人胚胎干细胞系H1接种于丝裂霉素C灭活后的人脐带间充质干细胞上,每隔5d进行一次传代。培养20代后,对人胚胎干细胞特性进行相关检测,包括细胞形态、碱性磷酸酶染色、相关多能性基因的表达、分化能力。结果从人脐带中分离出的间充质干细胞为梭形,呈平行排列生长或漩涡状生长;细胞高表达CD44、CD29、CD73、CD105、CD90、CD86、CD147、CD117,不表达CD14、CD38、CD133、CD34、CD45、HLA-DR;具有分化成脂肪细胞和成骨细胞的潜能。人胚胎干细胞在人脐带间充质干细胞饲养层上培养20代后,继续保持人胚胎干细胞的典型形态,碱性磷酸酶染色为阳性,免疫荧光染色显示OCT4、Nanog、SSEA4、TRA-1-81、TRA-1-60的表达为阳性,SSEA1表达为阴性,体外悬浮培养可以形成拟胚体。结论人脐带间充质干细胞可以作为人胚胎干细胞的饲养层细胞,支持其生长,并维持其未分化生长状态。 相似文献
16.
Merriwether DA 《Philosophical transactions of the Royal Society of London. Series B, Biological sciences》1999,354(1379):121-129
Archived blood fractions (plasma, settled red cells, white cells) have proved to be a rich and valuable source of DNA for human genetic studies. Large numbers of such samples were collected between 1960 and the present for protein and blood group studies, many of which are languishing in freezers or have already been discarded. More are discarded each year because the usefulness of these samples is not widely understood. Data from DNA derived from 10-35-year-old blood samples have been used to address the peopling of the New World and of the Pacific. Mitochondrial DNA haplotypes from studies using this source DNA support a single wave of migration into the New World (or a single source population for the New World), and that Mongolia was the likely source of the founding population. Data from Melanesia have shown that Polynesians are recent immigrants into the Pacific and did not arise from Melanesia. 相似文献
17.
Luisa Bertolini Richard H. Butler Roberto P. Revoltella 《Journal of cellular physiology》1984,119(1):65-70
CM-S is an autonomous cell line of human hemopoietic precursor cells inducible to monocyte-macrophage differentiation in response to appropriate inducing agents. CM-S cells produce factors that stimulate their own growth and proliferation, and are also capable of stimulating clonal proliferation of human, but not mouse, monocytic and granulocytic bone marrow progenitor cells in viscous medium. Preliminary purification steps have demonstrated at least two species, one of which (MW 30,000–50,000) retains both these activities, while the other (MW ≤ 10,000) apparently retains only the autostimulatory activity. CM-S cells could thus be a useful source for the purification of human colony stimulating factors (CSFs). CM-S cells also respond to factors present in human placenta conditioned medium, known to contain human CSF. This suggests that CM-S cells could provide a homogeneous target cell population for testing CSFs from other human sources. 相似文献
18.
M Noureddini J Verdi SA Mortazavi-Tabatabaei S Sharif A Azimi P Keyhanvar A Shoae-Hassani 《Cell biology international》2012,36(10):961-966
The potential of cell therapy is promising in nerve regeneration, but is limited by ethical considerations about the proper and technically safe source of stem cells. We report the successful differentiation of human EnSCs (endometrial stem cells) as a rich source of renewable and safe progenitors into high-efficiency cholinergic neurons. The extracellular signals of NGF (nerve growth factor) and bFGF (basic fibroblast growth factor) could induce cholinergic neuron differentiation. ChAT (choline acetyltransferase), MAP2 (microtubule associated protein 2) and NF-l (neurofilament L) increased after administration of bFGF and NGF to the EnSC cultures. trkC and FGFR2 (fibroblast growth factor receptor 2), which belong to the NGF and bFGF receptors respectively, were determined in populations of EnSCs. NGF, bFGF and their combination differentially influenced human EnSCs high efficiency differentiation. By inducing cholinergic neurons from EnSCs in a chemically defined medium, we could produce human neural cells without resorting to primary culture of neurons. This in vitro method provides an unlimited source of human neural cells and facilitates clinical applications of EnSCs for neurological diseases. 相似文献
19.
Pierre-Yves Collart-Dutilleul Franck Chaubron John De Vos Frédéric J Cuisinier 《World journal of stem cells》2015,7(7):1010-1021
Medical research in regenerative medicine and cell-based therapy has brought encouraging perspectives for the use of stem cells in clinical trials. Multiple types of stem cells, from progenitors to pluripotent stem cells, have been investigated. Among these, dental pulp stem cells (DPSCs) are mesenchymal multipotent cells coming from the dental pulp, which is the soft tissue within teeth. They represent an interesting adult stem cell source because they are recovered in large amount in dental pulps with non-invasive techniques compared to other adult stem cell sources. DPSCs can be obtained from discarded teeth, especially wisdom teeth extracted for orthodontic reasons. To shift from promising preclinical results to therapeutic applications to human, DPSCs must be prepared in clinical grade lots and transformed into advanced therapy medicinal products (ATMP). As the production of patient-specific stem cells is costly and time-consuming, allogenic biobanking of clinical grade human leukocyte antigen (HLA)-typed DPSC lines provides efficient innovative therapeutic products. DPSC biobanks represent industrial and therapeutic innovations by using discarded biological tissues (dental pulps) as a source of mesenchymal stem cells to produce and store, in good manufacturing practice (GMP) conditions, DPSC therapeutic batches. In this review, we discuss about the challenges to transfer biological samples from a donor to HLA-typed DPSC therapeutic lots, following regulations, GMP guidelines and ethical principles. We also present some clinical applications, for which there is no efficient therapeutics so far, but that DPSCs-based ATMP could potentially treat. 相似文献
20.
Hori Naohiro; Endo Yuichi; Okubo Kousaku; Murakawa Katsuji; Yokoyama Masahiro; Matoba Ryo; Matsubara Kenichi 《DNA research》1997,4(5):315-319
Expression sequence tags (EST) obtained by sequencing a randomlyprimed cDNA library and gene signatures (GS) obtained by sequencinga 3'-directed cDNA library can identify genes that are activein the source cells. Eight ESTs and ten GSs which representnovel human genes, except for one GS, and which have been assignedto human chromosome 11 were used to select cosmids from a chromosome11-specific cosmid library. These cosmids were regionally mappedusing the fluorescence in situ hybridization technique. 相似文献