derivation of chondrogenically-committed cells from human embryonic cells for cartilage tissue regeneration推导chondrogenically-committed细胞从人类胚胎细胞的软骨组织再生.pdfVIP
- 3
- 0
- 约6.29万字
- 约 10页
- 2017-09-01 发布于上海
- 举报
derivation of chondrogenically-committed cells from human embryonic cells for cartilage tissue regeneration推导chondrogenically-committed细胞从人类胚胎细胞的软骨组织再生
Derivation of Chondrogenically-Committed Cells from
Human Embryonic Cells for Cartilage Tissue
Regeneration
¤
Nathaniel S. Hwang, Shyni Varghese , Jennifer Elisseeff*
Department of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland, United States of America
Abstract
Background: Heterogeneous and uncontrolled differentiation of human embryonic stem cells (hESCs) in embryoid bodies
(EBs) limits the potential use of hESCs for cell-based therapies. More efficient strategies are needed for the commitment and
differentiation of hESCs to produce a homogeneous population of specific cell types for tissue regeneration applications.
Methodology/Principal Findings: We report here that significant chondrocytic commitment of feeder-free cultured human
embryonic stem cells (FF-hESCs), as determined by gene expression and immunostaining analysis, was induced by co-
culture with primary chondrocytes. Furthermore, a dynamic expression profile of chondrocyte-specific genes was observed
during monolayer expansion of the chondrogenically-committed cells. Chondrogenically-committed cells synergistically
responded to transforming growth factor-b1 (TGF-b1) and b1-integrin activating antibody by increasing tissue mass in
pellet culture. In addition, when encapsulated in hydrogels, these cells formed cartilage tissue both in vitro and in vivo. In
contrast, the absence of chondrocyte co-culture did not result in an expandable cell population from FF-hESCs.
Conclusions/Significance: The direct chondrocytic commitment of FF-hESCs can be induced by morphogenetic factors
from chondrocytes without EB formation and homogenous cartilage tissue can be formed in vitro and in vivo.
Citation: Hwang NS, Varghese S, Elisseeff J (2008) Derivation of Chondrogenically-Committed Cells from H
您可能关注的文档
- curcumin-loaded apotransferrin nanoparticles provide efficient cellular uptake and effectively inhibit hiv-1 replication in vitrocurcumin-loaded apotransferrin纳米粒子提供有效的体外细胞摄取和有效地抑制hiv - 1复制.pdf
- cx3cr1 is expressed by human b lymphocytes and meditates cx3cl1 driven chemotaxis of tonsil centrocytes二分法cx3cl1 cx3cr1所表达的是人类b淋巴细胞和驱动扁桃体中央细胞的趋化作用.pdf
- cxcl8 chemokines in teleost fish two lineages with distinct expression profiles during early phases of inflammationcxcl8趋化因子在硬骨鱼鱼两个血统与不同的表达谱在炎症的早期阶段.pdf
- cxc chemokine receptor 7 (cxcr7) regulates cxcr4 protein expression and capillary tuft development in mouse kidney科学家趋化因子受体7(cxcr7)调节趋化因子受体cxcr4蛋白表达和老鼠肾脏毛细血管丛发展.pdf
- cxcl10 is critical for the generation of protective cd8 t cell response induced by antigen pulsed cpg-odn activated dendritic cellscxcl10至关重要的一代保护性cd8 t细胞反应抗原引起的脉冲cpg-odn激活树突状细胞.pdf
- cutaneous larva migrans among devotees of the nallur temple in jaffna, sri lanka皮肤幼虫迁移动物在贾夫纳nallur神殿的信徒中,斯里兰卡.pdf
- cxcl12 chemokine expression and secretion regulates colorectal carcinoma cell anoikis through bim-mediated intrinsic apoptosiscxcl12趋化因子表达和分泌调节通过bim-mediated内在女性结直肠癌细胞凋亡.pdf
- custom design and analysis of high-density oligonucleotide bacterial tiling microarrays定制的设计和分析高密度寡核苷酸细菌花砖微阵列.pdf
- cxcl12cxcr4 axis triggers the activation of egf receptor and erk signaling pathway in csa-induced proliferation of human trophoblast cellscxcl12cxcr4轴触发egf受体的激活和erk信号通路csa-induced人类滋养层细胞的增殖.pdf
- cxcl17 expression by tumor cells recruits cd11b+gr1highf480? cells and promotes tumor progressioncxcl17肿瘤细胞表达的新兵cd11b + gr1highf480 细胞和促进肿瘤的进展.pdf
最近下载
- 安全个人防护用品使用教程PPT课件.pptx VIP
- 部编人教版三年级下册语文全册教案.docx VIP
- 学前教育学 教案.docx VIP
- 高级英语(第四版)1_教学课件Lesson 2 Blackmail.ppt VIP
- Thompson_Motif-Index(翻译版).doc VIP
- 2025年商汤科技商业计划书.pptx VIP
- 一文读懂2026年中央一号文件PPT关于锚定农业农村现代化+扎实推进乡村全面振兴的意见课件.pptx VIP
- BYD比亚迪交流充电桩ACC01-07G S50-F说明书.pdf
- 郑桂华《安塞腰鼓》课堂实录.docx VIP
- 实验六视图的操作.docx VIP
原创力文档

文档评论(0)