无异种培养条件对脂肪组织来源干细胞血管生成和脂肪生成分化特性的影响

IF 3.4 3区 环境科学与生态学 Q3 CELL & TISSUE ENGINEERING
Anne Therese Lauvrud , Maria Vittoria Giraudo , Rebecca Wiberg , Mikael Wiberg , Paul J. Kingham , Maria Brohlin
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引用次数: 0

摘要

导言在进行细胞疗法临床试验之前,了解细胞如何受到不同生长条件的影响以及找到最佳无异诺培养基配方非常重要。在这项研究中,我们调查了在无异诺条件下培养的脂肪组织源性干细胞(ASCs)的特性。方法将人脂肪抽吸样本消化后得到基质血管部分细胞,然后将其播种在 i) 补充 10 % (v/v) 胎牛血清 (FBS)的最小必需培养基-α (MEM-α)、ii) 补充 2 % (v/v) 人血小板裂解液 (PLT) 的 MEM-α 或 iii) PRIME-XV 间充质干细胞扩增 XSFM 无异种、无血清培养基 (XV)。对 ASCs 标记 CD73、CD90 和 CD105 以及推测的周细胞标记 CD146 进行流式细胞术检测。在多次传代培养过程中对生长率进行了监测,并在早期和扩大传代培养过程中进行了成脂分化。结果在 FBS 和 PLT 中培养的细胞生长速度相似,而在 XV 培养基中培养的细胞在培养 60 天后增殖速度明显加快。所有培养物的 CD73、CD90 和 CD105 阳性率均为 98%,而 XV 细胞的 CD146 表达明显更高。在 XV 培养基中培养的细胞成脂分化最明显,而在 PLT 培养基中培养的细胞与 FBS 培养基中培养的细胞相比则较差。用 PLT 培养的细胞中 IGF1 基因表达量最高,而用 XV 培养基培养的细胞中 IGF1 基因表达量比用 FBS 培养的细胞低 10 倍。相比之下,在 XV 培养基中培养的细胞的 HGF 基因表达量是在 FBS 培养基中培养的细胞的 90 倍。XV培养细胞的条件培养基显示出最强的血管生成活性,诱导了最大的内皮细胞网络形成和成熟。不同条件下的培养会改变 ASCs 的特性。由于在 XV 培养基中培养的细胞显示出最佳的脂肪生成和血管生成特性,因此这可能是制备重建外科应用(如细胞辅助脂肪移植)所需细胞的首选培养基配方。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The influence of xeno-free culture conditions on the angiogenic and adipogenic differentiation properties of adipose tissue-derived stem cells

Introduction

Before performing cell therapy clinical trials, it is important to understand how cells are influenced by different growth conditions and to find optimal xeno-free medium formulations. In this study we have investigated the properties of adipose tissue-derived stem cells (ASCs) cultured under xeno-free conditions.

Methods

Human lipoaspirate samples were digested to yield the stromal vascular fraction cells which were then seeded in i) Minimum Essential Medium-α (MEM-α) supplemented with 10 % (v/v) fetal bovine serum (FBS), ii) MEM-α supplemented with 2 % (v/v) human platelet lysate (PLT) or iii) PRIME-XV MSC expansion XSFM xeno-free, serum free medium (XV). Flow cytometry for ASCs markers CD73, CD90 and CD105 together with the putative pericyte marker CD146 was performed. Growth rates were monitored over multiple passages and adipogenic differentiation performed at early and expanded passage culture. Growth factor gene expression was analyzed and an in vitro angiogenesis assay performed.

Results

Cells in FBS and PLT grew at similar rates whereas the cells cultured in XV medium proliferated significantly faster up to 60 days in culture. All cultures were >98 % positive for CD73, CD90 and CD105, whereas CD146 expression was significantly higher in XV cells. Adipogenic differentiation was most pronounced in cells which had been cultured in XV medium whilst cells grown in PLT were inferior compared with cells from the FBS cultures. IGF1 gene expression was highest in cells cultured in PLT whilst cells grown in XV medium showed 10-fold lower expression compared with FBS cells. In contrast, HGF gene expression was 90-fold greater in cells cultured in XV medium compared with those cultured in FBS. Conditioned medium from XV cultured cells showed the most angiogenic activity, inducing the greatest endothelial cell network formation and maturation.

Conclusion

Culture under different conditions alters the ASCs characteristics. Since cells cultured in XV medium showed the best adipogenic and angiogenic profile this might be a preferred medium formulation for preparing cells required for reconstructive surgical applications such as cell-assisted fat grafting.
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来源期刊
Regenerative Therapy
Regenerative Therapy Engineering-Biomedical Engineering
CiteScore
6.00
自引率
2.30%
发文量
106
审稿时长
49 days
期刊介绍: Regenerative Therapy is the official peer-reviewed online journal of the Japanese Society for Regenerative Medicine. Regenerative Therapy is a multidisciplinary journal that publishes original articles and reviews of basic research, clinical translation, industrial development, and regulatory issues focusing on stem cell biology, tissue engineering, and regenerative medicine.
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