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Collagenase, Type 2

胶原酶II

Company: Worthington Biochemical
Catalog#: LS004176
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Isolation, Culturing, and Differentiation of Primary Myoblasts from Skeletal Muscle of Adult Mice
Author:
Date:
2017-05-05
[Abstract]  Myogenesis is a multi-step process that leads to the formation of skeletal muscle during embryonic development and repair of injured myofibers. In this process, myoblasts are the main effector cell type which fuse with each other or to injured myofibers leading to the formation of new myofibers or regeneration of skeletal muscle in adults. Many steps of myogenesis can be recapitulated through in vitro differentiation of myoblasts into myotubes. Most laboratories use immortalized myogenic cells lines that also differentiate into myotubes. Although these cell lines have been found quite useful to delineating the regulatory mechanisms of myogenesis, they often show a great degree of variability depending on the origin of the cells and culture conditions. Primary myoblasts have been ... [摘要]  造血是一种多步骤过程,导致在损伤的肌纤维的胚胎发育和修复期间骨骼肌的形成。在这个过程中,成肌细胞是主要的效应细胞类型,彼此融合或损伤肌纤维,导致新成肌纤维的形成或成年人骨骼肌的再生。通过体外成骨细胞分化成肌管可以概括出许多发生肌肉发育的步骤。大多数实验室使用也分化成肌管的永生化肌原细胞系。虽然已经发现这些细胞系对于描绘造血的调节机制非常有用,但是它们通常依赖于细胞的来源和培养条件而显示出很大的变异性。原代成肌细胞被认为是体外研究肌生成的最生理学相关模型。然而,由于成体骨骼肌的丰度低,原代成肌细胞的分离在技术上是有挑战性的。在本文中,我们描述了一种用于从小鼠的成年骨骼肌分离原代成肌细胞的改进方案。我们还描述了其培养和分化成肌管的方法。


背景 造血是一个复杂而高度协调的过程,其涉及多潜能中胚层细胞的测定,以产生成肌细胞,成肌细胞从细胞周期中排出,以及它们最终分化为骨骼肌纤维。 Myogen-5,MyoD,myogenin和MRF4的基因螺旋 - 环 - 螺旋转录因子的一组基因调控因子(MRFs)的顺序表达调控。 Myf-5和MyoD是成肌细胞形成,增殖和存活所需的主要MRFs,而其他MRF(如肌细胞生成素和MRF-4)在肌发生过程中起作用迟发,激活收缩蛋白和其他结构和代谢蛋白的基因表达(白金汉,2003; ...

Mimicking Angiogenesis in vitro: Three-dimensional Co-culture of Vascular Endothelial Cells and Perivascular Cells in Collagen Type I Gels
Author:
Date:
2017-04-20
[Abstract]  Angiogenesis defines the process of formation of new vascular structures form existing blood vessels, involved during development, repair processes like wound healing but also linked to pathological changes. During angiogenic processes, endothelial cells build a vascular network and recruit perivascular cells to form mature, stable vessels. Endothelial cells and perivascular cells secret and assemble a vascular basement membrane and interact via close cell-cell contacts. To mimic these processes in vitro we have developed a versatile three-dimensional culture system where perivascular cells (PVC) are co-cultured with human umbilical cord vascular endothelial cells (HUVEC) in a collagen type I gel. This co-culture system can be used to determine biochemical and cellular processes ... [摘要]  血管发生定义了形成现有血管的新血管结构的形成过程,涉及发育过程中的修复过程,如伤口愈合,还与病理变化有关。 在血管生成过程中,内皮细胞建立血管网络并招募血管周围细胞以形成成熟稳定的血管。 内皮细胞和血管周围细胞秘密并组装血管基底膜,并通过细胞间接触进行相互作用。 为了体外模拟这些过程,我们开发了一种通用的三维培养系统,其中血管周围细胞(PVC)与胶原I型凝胶中的人脐带血管内皮细胞(HUVEC)共培养。 这种共培养系统可用于通过广泛的分析选项来确定新生血管生成事件期间的生物化学和细胞过程。
【背景】内皮细胞和血管周围细胞之间的协调相互作用对于根据给定组织内的局部需要形成稳定的血管网是非常重要的。多个分子组分有助于相互作用,但仍然很少了解。需要各种生长因子来吸引内皮细胞到低氧浓度的位点,并建立新的血管,然后被血管周围细胞覆盖。两种细胞类型相互作用以分泌特定的细胞外基质并稳定新形成的血管。在过去已经建立了多个测定法来分析二维基质胶底物上的血管细胞相互作用和血管样网络形成,但是这些测定在三维细胞内提供关于血管内血管周围细胞相互作用和血管基底膜形成的初始步骤的信息是有限的维度微环境。此外,缺乏适合于培养实验的良好表征的血管周围细胞。
我们以前分离出具有血管周围特征的细胞,因为它们表达周细胞特异性标记,产生和分泌细胞外基质蛋白并在体内刺激血管生成过程(Brachvogel等,2005和2007)。这些细胞用于与人脐静脉内皮细胞建立共培养系统,并研究三维微环境中两种细胞类型相互作用后新生血管发生的关键步骤(Pitzler等,2016; ...

Isolation, Culture, and Staining of Single Myofibers
Author:
Date:
2016-10-05
[Abstract]  Adult skeletal muscle regeneration is orchestrated by a specialized population of adult stem cells called satellite cells, which are localized between the basal lamina and the plasma membrane of myofibers. The process of satellite cell-activation, proliferation, and subsequent differentiation that occurs during muscle regeneration can be recapitulated ex vivo by isolation of single myofibers from skeletal muscles and culturing them under suspension conditions. Here, we describe an improved protocol to evaluate ex vivo satellite cells activation through isolation of single myofibers from extensor digitorum longus (EDL) muscle of mice and culturing and staining of myofiber-associated satellite cells with the markers of self-renewal, proliferation, and differentiation. [摘要]  成年骨骼肌再生由被称为卫星细胞的成人干细胞的专门群体协调,其被定位在基底层和肌纤维的质膜之间。在肌肉再生期间发生的卫星细胞激活,增殖和随后分化的过程可以通过从骨骼肌中分离单个肌纤维并在悬浮条件下培养它们而在体外重现。在这里,我们描述了一种改进的协议,通过从小鼠的伸肌腱长肌(EDL)肌肉中分离单个肌纤维来评价离体细胞的活化,并培养和染色肌纤维相关的卫星细胞的标记物自我更新,增殖和分化。

[背景] 虽然骨骼肌是一种完全分化的有丝分裂后组织,但是它保持了内在的能力,以对遗传和获得性肌肉纤维损伤的形式Grand和Rudnicki,2007)。成年人的肌肉再生由称为卫星细胞的干细胞群体介导,所述细胞位于有丝分裂静止状态的肌纤维的基底层和肌纤维膜之间(Le Grand和Rudnicki,2007)。响应于肌肉创伤,卫星细胞变得活化和增殖以产生与预先存在的纤维融合的成肌细胞,并彼此相互修复或产生新的肌纤维。一小部分卫星细胞不分化,而是重新进入静止以维持干细胞库。所有哺乳动物物种的卫星细胞表达配对盒(Pax)转录因子Pax7,其也用作确定与其他生肌因子如MyoD相关的卫星细胞命运的关键标记(Le Grand和Rudnicki,2007; et al。,2006; Kuang and Rudnicki,2008)。
  可以通过肌纤维外植体的悬浮培养部分地重现关于卫星细胞活化,增殖和分化的肌肉再生的体内过程(Rosenblatt等人,1995; ...

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