Investigate the co-culture effects of BM-mesenchymal stem cells on the promotion of apoptotic pathways of CD34+leukemic stem cells.

IF 2.2 4区 工程技术 Q3 PHARMACOLOGY & PHARMACY
Bioimpacts Pub Date : 2025-08-25 eCollection Date: 2025-01-01 DOI:10.34172/bi.31302
Mei Ding, Chuanhua Jia
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引用次数: 0

Abstract

Introduction: The potential clinical application of mesenchymal stem cells (MSCs) in cell-based treatment makes them particularly interesting. The use of MSC-engaged therapies in cancer treatment is becoming more and more promising. Although the specifics of their activity have not yet been conclusively established, a variety of growth factors released by these cells are known to provide such multifunctional qualities.

Methods: Through the measurement of cytokine levels, Annexin-V, and possible signaling pathways linked to apoptosis, we have assessed the impact of MSCs on CD34+leukemic stem cells (LSCs) enriched from the KG1-a cell line. Additionally, culture medium was taken from the experimental and control groups for the IL-2 and IL-4 measurement following a 7-day co-culture.

Results: Co-culture conditions were observed to promote early and late apoptosis, although this increase just was statistically significant in late apoptosis. The co-cultured conditioned media clearly showed a large amount of IL-2, but there was an insignificant rise in IL-4. Also, MSCs significantly increased the protein expression of P16, P21, and p-P38 and significantly decreased C-Myc, and TERC.

Conclusion: It can be concluded that the mentioned effects of IL-2 cytokine released from MSCs on CD34+LSCs maybe were applied by the components of P16, P21, and p-P38, C-Myc signaling pathways.

探讨脑-间充质干细胞共培养对促进CD34+白血病干细胞凋亡通路的影响。
间充质干细胞(MSCs)在基于细胞的治疗中的潜在临床应用使它们特别有趣。利用间充质干细胞治疗癌症的前景越来越广阔。虽然其活性的具体细节尚未最终确定,但已知这些细胞释放的各种生长因子具有这种多功能特性。方法:通过测量细胞因子水平、膜联蛋白v和与凋亡相关的可能信号通路,我们评估了MSCs对KG1-a细胞系富集的CD34+白血病干细胞(LSCs)的影响。另外,在共培养7天后,分别取实验组和对照组的培养基进行IL-2和IL-4的测定。结果:共培养条件对早期和晚期细胞凋亡均有促进作用,但仅对晚期细胞凋亡有统计学意义。共培养条件培养基中IL-2明显增多,IL-4明显升高。此外,MSCs显著提高了P16、P21和p-P38的蛋白表达,显著降低了C-Myc和TERC的表达。结论:MSCs释放IL-2细胞因子对CD34+LSCs的作用可能是通过P16、P21、p-P38、C-Myc信号通路的组分发挥作用的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Bioimpacts
Bioimpacts Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.80
自引率
7.70%
发文量
36
审稿时长
5 weeks
期刊介绍: BioImpacts (BI) is a peer-reviewed multidisciplinary international journal, covering original research articles, reviews, commentaries, hypotheses, methodologies, and visions/reflections dealing with all aspects of biological and biomedical researches at molecular, cellular, functional and translational dimensions.
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