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The fate of bone marrow-derived cells carrying a polycystic kidney disease mutation in the genetically normal kidney

机译:遗传性正常肾脏中携带多囊肾疾病突变的骨髓来源细胞的命运

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Background Polycystic Kidney Disease (PKD) is a genetic condition in which dedifferentiated and highly proliferative epithelial cells form renal cysts and is frequently treated by renal transplantation. Studies have reported that bone marrow-derived cells give rise to renal epithelial cells, particularly following renal injury as often occurs during transplantation. This raises the possibility that bone marrow-derived cells from a PKD-afflicted recipient could populate a transplanted kidney and express a disease phenotype. However, for reasons that are not clear the reoccurrence of PKD has not been reported in a genetically normal renal graft. We used a mouse model to examine whether PKD mutant bone marrow-derived cells are capable of expressing a disease phenotype in the kidney. Methods Wild type female mice were transplanted with bone marrow from male mice homozygous for a PKD-causing mutation and subjected to renal injury. Y chromosome positive, bone marrow-derived cells in the kidney were assessed for epithelial markers. Results Mutant bone marrow-derived cells were present in the kidney. Some mutant cells were within the bounds of the tubule or duct, but none demonstrated convincing evidence of an epithelial phenotype. Conclusions Bone marrow-derived cells appear incapable of giving rise to genuine epithelial cells and this is the most likely reason cysts do not reoccur in kidneys transplanted into PKD patients.
机译:背景技术多囊肾病(PKD)是一种遗传疾病,其中去分化和高度增殖的上皮细胞形成肾囊肿,并经常通过肾移植进行治疗。研究报道,骨髓来源的细胞会产生肾上皮细胞,特别是在移植过程中经常发生的肾损伤后。这增加了来自受PKD影响的受体的骨髓来源的细胞可能会植入移植的肾脏并表达疾病表型的可能性。但是,由于尚不清楚的原因,尚未在遗传上正常的肾移植物中报道PKD的复发。我们使用小鼠模型来检查PKD突变体骨髓来源的细胞是否能够在肾脏中表达疾病表型。方法野生型雌性小鼠从纯合的雄性小鼠的骨髓中移植导致PKD的突变,并遭受肾损伤。评估肾中Y染色体阳性,骨髓来源的细胞的上皮标记。结果肾脏中存在突变的骨髓来源的细胞。一些突变细胞位于肾小管或导管的界限内,但没有一个显示出令人信服的上皮表型证据。结论骨髓来源的细胞似乎无法产生真正的上皮细胞,这是移植到PKD患者肾脏中囊肿未复发的最可能原因。

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