[Study of migration and distribution of bone marrow cells transplanted animals with B16 melanoma ].

A F Poveshchenko, A O Solovieva, K E Zubareva, D N Strunkin, O B Gricyk, O V Poveshchenko, A V Shurlygina, V I Konenkov
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Abstract

Purpose. Reveal features migration and distribution of syngeneic bone marrow cells (BMC) and subpopulations (MSC) after transplantation into the recipient carrier B16 melanoma bodies. Methods. We used mouse male and female C57BL/6 mice. Induction of Tumor Growth: B16 melanoma cells implanted subcutaneously into right hind paw of female C57BL/6 mice at a dose of 2.5 x 105 cells / mouse. migration study in vivo distribution and BMC and MSC was performed using genetic markers - Y-chromosome specific sequence line male C57Bl/6 syngeneic intravenous transplantation in females using the polymerase chain reaction (PCR) in real time on Authorized Termal Cycler - Light Cycler 480 II / 96 (Roche). Introduction suspension of unseparated bone marrow cells, mesenchymal stem cells from donor to recipient male mice (syngeneic recipient female C57BL/6), followed by isolation of recipients of organs was performed at regular intervals, then of organ recipients isolated DNA. Results. It was shown that bone marrow cells positive for Y-chromosome in migrate lymphoid (lymph nodes, spleen, bone marrow) or in non-lymphoid organs (liver, heart, brain, skin) syngeneic recipients. In addition to the migration of cells from the bone marrow to other organs, there is a way back migration of cells from the circulation to the bone marrow. B16 melanoma stimulates the migration of transplanted MSCs and BMC in bone marrow. It is found that tumor growth enhanced migration of transplanted bone marrow cells, including populations of MSCs in the bone marrow. In the early stages of tumor formation MSC migration activity higher than the BMC. In the later stages of tumor formation undivided population of bone marrow cells migrate to the intense swelling compared with a population of MSCs. Conclusion. The possibility of using bone marrow MSCs for targeted therapy of tumor diseases, because migration of MSCs in tumor tissue can be used to effectively deliver anticancer drugs.

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[B16黑色素瘤移植动物骨髓细胞迁移分布的研究]。
目的。揭示同基因骨髓细胞(BMC)和亚群(MSC)移植到受体载体B16黑色素瘤体后的迁移和分布特征。方法。我们选用雄性和雌性C57BL/6小鼠。诱导肿瘤生长:雌性C57BL/6小鼠右后爪皮下植入B16黑色素瘤细胞,剂量为2.5 × 105个/只。采用遗传标记-雄性y染色体特异性序列系C57Bl/6同基因静脉移植在罗氏授权的Termal Cycler - Light Cycler 480 II / 96上进行实时聚合酶链反应(PCR),对雌性进行体内分布和BMC和MSC迁移研究。将未分离的骨髓细胞、间充质干细胞(同种雌性受体C57BL/6)从供体小鼠中引入悬液,然后定期分离器官受体,然后分离器官受体的DNA。结果。结果表明,移行淋巴细胞(淋巴结、脾脏、骨髓)和非淋巴器官(肝、心、脑、皮肤)同基因受者骨髓细胞y染色体阳性。除了将细胞从骨髓迁移到其他器官之外,还有一种方法将细胞从循环系统迁移回骨髓。B16黑色素瘤刺激移植骨髓间充质干细胞和BMC的迁移。研究发现,肿瘤的生长增强了移植骨髓细胞的迁移,包括骨髓中MSCs的群体。在肿瘤形成早期,MSC的迁移活性高于BMC。在肿瘤形成的后期,未分化的骨髓细胞群与间充质干细胞群相比迁移到强烈肿胀处。结论。利用骨髓间充质干细胞靶向治疗肿瘤疾病的可能性,因为骨髓间充质干细胞在肿瘤组织中的迁移可以用来有效地传递抗癌药物。
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[Study of migration and distribution of bone marrow cells transplanted animals with B16 melanoma ]. [Reprogrammed M1 macrophages with inhibited STAT3, STAT6 and/or SMAD3 extends lifespan of mice with experimental carcinoma]. [Activation of regeneration of red and white pulp of the spleen after the combined transplantation of HSC and MSCS in terms of exposure to ionizing radiation]. [Effect of conditioned medium from mesenchymal stem cells on regeneration of endothelium at HCl-induced damage trachea in rats]. [Matrix metalloproteinase-1, -8, -9 and the risk of cardiovascular complications in patients with CHD before and after myocardial revascularization].
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