细胞内透明质酸合成损害糖尿病患者造血功能,可通过肝素预防

A. Wang, V. Hascall
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摘要

摘要糖尿病中的高血糖会导致造血功能受损,这是导致晚期糖尿病慢性并发症的骨髓(BM)的一个重要后果。与糖尿病(DM)病理相关的血细胞改变已被仔细和广泛地记录,但其潜在机制仍不清楚。我们最近的出版物表明,高血糖分裂的骨髓祖细胞异常合成透明质酸(HA)是相关的中心机制。这项研究表明,在高血糖状态下从祖细胞分裂出来的巨噬细胞具有促炎性(Mpi),并且低浓度肝素(~20nM)的存在阻止了细胞内HA的合成并促进了组织修复(Mtr)表型。在这里,我们简要介绍了我们对细胞内透明质酸合成异常如何损害糖尿病造血及其肝素调节的新研究
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Intracellular Hyaluronan Synthesis Impairs Hematopoiesis in Diabetes that can be Prevented by Heparin
in Abstract Hyperglycemia in diabetes induces impairment of hematopoiesis, an important consequence in bone marrow (BM) that contributes to chronic complications in advanced diabetes. The alterations to blood cells associated with diabetes mellitus (DM) pathologies have been carefully and extensively documented, but the underlying mechanism(s) is still unclear. Our recent publication indicates that aberrant intracellular synthesis of hyaluronan (HA) by hyperglycemic dividing BM progenitors is the central mechanism involved. This study demonstrated that macrophages that divided from progenitor cells in hyperglycemia are pro-inflammatory (Mpi) and that the presence of low concentrations of heparin (~20 nM) prevented the intracellular HA synthesis and promoted a tissue repair (Mtr) phenotype. Here, we briefly describe how our new studies of abnormal intracellular hyaluronan synthesis impairs hematopoiesis in diabetes and its regulation by heparin
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