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首页> 外文期刊>American Journal of Pathology: Official Publication of the American Association of Pathologists >Proteoglycan 4, a novel immunomodulatory factor, regulates parathyroid hormone actions on hematopoietic cells.
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Proteoglycan 4, a novel immunomodulatory factor, regulates parathyroid hormone actions on hematopoietic cells.

机译:蛋白聚糖4是一种新型的免疫调节因子,可调节甲状旁腺激素对造血细胞的作用。

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Proteoglycan 4 (PRG4), a critical protective factor in articular joints, is implicated in hematopoietic progenitor cell expansion and megakaryopoiesis. PRG4 loss-of-function mutations result in camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome, which is characterized primarily by precocious joint failure. PRG4 was identified as a novel parathyroid hormone (PTH) responsiveness gene in osteoblastic cells in bone, and was investigated as a potential mediator of PTH actions on hematopoiesis. Sixteen-week-old Prg4(-/-) mutant and Prg4(+/+) wild-type mice were treated daily with intermittent PTH (residues 1-34) or vehicle for 6 weeks. At 22 weeks of age, Prg4 mutant mice had increased peripheral blood neutrophils and decreased marrow B220(+) (B-lymphocytic) cells, which were normalized by PTH. The PTH-induced increase in marrow Lin(-)Sca-1(+)c-Kit(+) (hematopoietic progenitor) cells was blunted in mutant mice. Basal and PTH-stimulated stromal cell-derived factor-1 (SDF-1) was decreased in mutant mice, suggesting SDF-1 as a candidate regulator of proteoglycan 4 actions on hematopoiesis in vivo. PTH stimulation of IL-6 mRNA was greater in mutant than in wild-type calvaria and bone marrow, suggesting a compensatory mechanism in the PTH-induced increase in marrow hematopoietic progenitor cells. In summary, proteoglycan 4 is a novel PTH-responsive factor regulating immune cells and PTH actions on marrow hematopoietic progenitor cells.
机译:蛋白聚糖4(PRG4)是关节中的关键保护因子,与造血祖细胞扩增和巨核细胞生成有关。 PRG4功能丧失的突变会导致Campodactyly关节病-柯萨伐拉性心包炎(CACP)综合征,其主要特征是性早熟关节衰竭。 PRG4被鉴定为骨骼中成骨细胞中一种新型的甲状旁腺激素(PTH)反应基因,并已被研究为PTH对造血作用的潜在介体。每天用间歇性PTH(残基1-34)或溶媒治疗16周龄的Prg4(-/-)突变体和Prg4(+ / +)野生型小鼠6周。在22周龄时,Prg4突变小鼠的外周血中性粒细胞增加,骨髓B220(+)(B-淋巴细胞)细胞减少,PTH可将其正常化。在突变小鼠中,PTH诱导的骨髓Lin(-)Sca-1(+)c-Kit(+)(造血祖细胞)细胞的增加受到抑制。在突变小鼠中基础和PTH刺激的基质细胞衍生因子1(SDF-1)减少,表明SDF-1作为蛋白聚糖4在体内对造血作用的候选调节剂。 PTH刺激突变体中IL-6 mRNA的作用大于野生型颅盖和骨髓,提示PTH诱导的骨髓造血祖细胞增加具有补偿机制。总之,蛋白聚糖4是一种新型的PTH反应因子,可调节免疫细胞和PTH对骨髓造血祖细胞的作用。

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