دورية أكاديمية

[Release of Exosomes Derived from Leukocyte-Depleted Red Cell Suspension and Its Regulation on Hematological Tumor Cells].

التفاصيل البيبلوغرافية
العنوان: [Release of Exosomes Derived from Leukocyte-Depleted Red Cell Suspension and Its Regulation on Hematological Tumor Cells].
المؤلفون: Huang HB; Department of Blood Transfusion, Fujian Medical University Union Hospital, Fuzhou 350001, Fujian Province, China., Fan LP; Department of Blood Transfusion, Fujian Medical University Union Hospital, Fuzhou 350001, Fujian Province, China., Lin QY; Department of Blood Transfusion, Fujian Medical University Union Hospital, Fuzhou 350001, Fujian Province, China., Huang HW; Department of Blood Transfusion, Fujian Medical University Union Hospital, Fuzhou 350001, Fujian Province, China., Fu DH; Department of Blood Transfusion, Fujian Medical University Union Hospital, Fuzhou 350001, Fujian Province, China,Department of Hematology, Fujian Medical University Union Hospital, Fuzhou 350001, Fujian Province, China,E-mail: fudanhui@189.cn.
المصدر: Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2022 Aug; Vol. 30 (4), pp. 1188-1192.
نوع المنشور: Journal Article
اللغة: Chinese
بيانات الدورية: Publisher: Zhongguo shi yan xue za zhi she Country of Publication: China NLM ID: 101084424 Publication Model: Print Cited Medium: Print ISSN: 1009-2137 (Print) Linking ISSN: 10092137 NLM ISO Abbreviation: Zhongguo Shi Yan Xue Ye Xue Za Zhi Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Beijing : Zhongguo shi yan xue za zhi she,
مواضيع طبية MeSH: Exosomes*/metabolism , Hematologic Neoplasms*/metabolism, Cell Proliferation ; Erythrocytes ; Humans ; Leukocytes
مستخلص: Objective: To investigate the release of exosome (Exo) from leukocyte-depleted red cell suspension (LDRCS) at different storage time and its regulation on proliferation of hematological tumor cells and possible mechanism.
Methods: The Exo (RBC-Exo) in LDRCS at different storage time was obtained by ultracentrifugation, and the morphology and immunological marker of RBC-Exo were detected by transmission electron microscopy and Western blot, respectively. The particle size distribution of RBC-Exo in LDRCS at different storage time was detected by Dynamic Light Scattering. CCK-8 assay was used to explore the effect of RBC-Exo on hematological tumor cell proliferation. Western blot was used to detect the expression of proliferation-related proteins in hematological tumor cells after co-culture with RBC-Exo.
Results: RBC-Exo was isolated, which was characterized by cup-like shape, particle size distribution ranged from 20 to 200 nm, CD63/TSG101 enriched, Calnexin negative, CD235a positive and CD41 negative. The particle size distribution of RBC-Exo from LDRCS between middle was not significantly different and late stored stage. But the particle size distribution of RBC-Exo at middle-late stored stage(>14 d) was larger than that at early stored stage (≤14 days). Compared with the control group, RBC-Exo could significantly promote the proliferation of HBL1, U2932 and Jurkat cells. Compared with the control group, the cycle-related protein P21 was significantly down-regulated in HBL1, U2932 and Jurkat cells after co-culture with RBC-Exo for 3 days, while the anti-apoptotic protein BCL-2 was not changed significantly.
Conclusion: The morphology of RBC-Exo from LDRCS at middle-late stored stage was different from that at early stored stage. RBC-Exo could promote the proliferation of hematological tumor cells, possibly by regulating the expression of cycle-associated protein P21.
فهرسة مساهمة: Keywords: exosome; leukocyte-depleted red cell suspension; proliferation; tumor cell
Local Abstract: [Publisher, Chinese] 去白细胞悬浮红细胞来源外泌体的释放及其对血液肿瘤细胞的调控. [Publisher, Chinese] 探讨不同储存时间去白细胞悬浮红细胞(LDRCS)中外泌体(exosome,Exo)的释放及其对血液肿瘤细胞增殖的调控与可能机制. [Publisher, Chinese] 应用超高速离心方法获得不同储存时间的LDRCS中Exo(RBC-Exo),采用透射电镜术、蛋白免疫印迹法分别对RBC-Exo的形态、免疫标记进行检测。采用动态光散射检测不同储存时间LDRCS中RBC-Exo的粒径分布变化。采用CCK-8法检测RBC-Exo对血液肿瘤细胞增殖的影响。采用蛋白免疫印迹法检测与RBC-Exo共培养后血液肿瘤细胞内增殖相关蛋白的表达变化. [Publisher, Chinese] 分离出呈类杯状、粒径分布于20-200 nm、CD63/TSG101富集、Calnexin阴性、CD235a阳性、CD41阴性的RBC-Exo。储存中晚期(>14 d)LDRCS中RBC-Exo粒径分布无显著差异,但显著大于储存早期(储存≤14 d)的RBC-Exo。与对照组相比,RBC-Exo可以明显促进血液肿瘤细胞HBL1、U2932和Jurkat的增殖。与RBC-Exo共培养3 d的HBL1、U2932和Jurkat细胞中周期相关蛋白P21的表达较对照组明显下调,而抗凋亡蛋白BCL-2并无明显变化. [Publisher, Chinese] 储存中晚期的LDRCS中RBC-Exo形态与储存早期存在差异。RBC-Exo可以促进血液肿瘤细胞的增殖,其机制可能是通过调节周期相关蛋白P21的表达.
تواريخ الأحداث: Date Created: 20220818 Date Completed: 20220822 Latest Revision: 20220822
رمز التحديث: 20240628
DOI: 10.19746/j.cnki.issn.1009-2137.2022.04.033
PMID: 35981382
قاعدة البيانات: MEDLINE
الوصف
تدمد:1009-2137
DOI:10.19746/j.cnki.issn.1009-2137.2022.04.033