控制干细胞的分化通过生物活性失序的线索
Yujie Zhang1, Murielle Rémy1, Evgeny Apartsin1
1Univ. Bordeaux, CNRS, Bordeaux INP, CBMN, UMR 5248, F-33600 Pessac, France. marie-christine.durrieu@inserm.fr.
Biomaterials science
|August 21, 2023
概括
在PET表面上随机微型的可以增强人间介质干细胞 (hMSC) 的骨质分化,促进骨再生. 这种生物材料方法改善了用于组织工程应用的细胞行为.
科学领域:
- 生物材料科学 生物材料科学
- 组织工程是组织工程.
- 细胞生物学 细胞生物学
背景情况:
- 骨组织工程旨在通过支架,细胞和生长因子再生骨.
- 生物模拟性支架模仿细胞外基质 (ECM),用于研究细胞-ECM相互作用.
- 在活体中,细胞微环境对细胞行为进行了关键调节.
研究的目的:
- 研究聚合物表面独特的生物活性微/纳米模式是否增强人间介质干细胞 (hMSC) 差异化.
- 使用功能化的PET表面促进hMSC粘附和骨质分化.
- 探索随机微模式对细胞形态和血统承诺的影响.
主要方法:
- 聚乙烯二甲 (PET) 表面被RGD和BMP-2模仿激活和功能化,使用喷雾技术.
- 表面特征包括原子力显微镜,光显微镜和X射线光电谱学.
- 通过通过免疫光测量量骨质母细胞和骨细胞标志物表达的量化来评估hMSC差异化.
主要成果:
- 在DMEM中14天后,带有RGD和BMP-2的无序微型图案表面比同质表面显示出更高的骨质母细胞标志物表达.
- 在骨质分化介质 (ODM) 中在随机微型的PET表面上培养的hMSCs表现出加速分化.
- 在PET表面上播种的hMSC中观察到骨质细胞标记物的表达,在ODM中随机微模式.
结论:
- 在PET表面上随机微模式生物活性有效促进hMSC骨质的分化.
- 这种方法为开发用于骨再生的先进生物材料提供了一个有前途的战略.
- 这项研究强调了量身定制的表面地形在指导组织工程细胞命运方面的潜力.
相关概念视频
Stem Cell Niche
5.2K
The stem cell niche is the dynamic microenvironment where stem cells reside. Inside these niches, the cells may remain undifferentiated, undergo high self-renewal, or become lineage-specific progenitors. Stem cells coexist with other niche cells, such as stromal cells. They also interact closely with the ECM. Cell-cell and cell-matrix communication occur via adhesion molecules or soluble factors that signal the stem cells and determine their fate. Stromal cells also provide survival signals to...
5.2K
Stem Cell Culture
5.2K
Stem cell research aims to find ways to use stem cells to regenerate and repair cellular damage. Over time, most adult cells undergo the wear and tear of aging and lose their ability to divide and repair themselves. Stem cells do not display a particular morphology or function. Adult stem cells, which exist as a small subset of cells in most tissues, keep dividing and can differentiate into a number of specialized cells generally formed by that tissue. These cells enable the body to renew and...
5.2K
Forced Transdifferentiation
1.9K
Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
Artificial...
Artificial...
1.9K
iPS Cell Differentiation
2.7K
The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
2.7K
Maintenance of the ES Cell State
2.2K
The cells of the blastocyst inner cell mass only remain pluripotent for a short time. This state of pluripotency and self-renewal can be maintained in embryonic stem (ES) cell culture by adding specific chemicals or growth factors to ensure the cells can continue dividing and later differentiate into different cell types. In some cases, the cells are grown on a feeder layer of differentiated cells, which provides the growth factors and extracellular matrix components necessary for stem cell...
2.2K
Regulation of Hematopoietic Stem Cells
3.2K
All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...
3.2K


