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本文引用的文献

1
Distinct macrophage phenotypes contribute to kidney injury and repair.不同的巨噬细胞表型有助于肾脏损伤和修复。
J Am Soc Nephrol. 2011 Feb;22(2):317-26. doi: 10.1681/ASN.2009060615.
2
Macrophages and immunologic inflammation of the kidney.巨噬细胞与肾脏的免疫炎症。
Semin Nephrol. 2010 May;30(3):234-54. doi: 10.1016/j.semnephrol.2010.03.003.
3
Activator of G protein signaling 3 promotes epithelial cell proliferation in PKD.G 蛋白信号转导激活因子 3 促进 PKD 中的上皮细胞增殖。
J Am Soc Nephrol. 2010 Aug;21(8):1275-80. doi: 10.1681/ASN.2009121224. Epub 2010 May 20.
4
Molecular advances in autosomal dominant polycystic kidney disease.常染色体显性遗传性多囊肾病的分子进展。
Adv Chronic Kidney Dis. 2010 Mar;17(2):118-30. doi: 10.1053/j.ackd.2010.01.002.
5
Loss of oriented cell division does not initiate cyst formation.定向细胞分裂的丧失并不会引发囊肿的形成。
J Am Soc Nephrol. 2010 Feb;21(2):295-302. doi: 10.1681/ASN.2009060603. Epub 2009 Dec 3.
6
Bone marrow Ly6Chigh monocytes are selectively recruited to injured kidney and differentiate into functionally distinct populations.骨髓中Ly6C高表达的单核细胞被选择性募集到受损肾脏,并分化为功能不同的细胞群。
J Immunol. 2009 Nov 15;183(10):6733-43. doi: 10.4049/jimmunol.0901473. Epub 2009 Oct 28.
7
Autosomal dominant polycystic kidney disease: the last 3 years.常染色体显性多囊肾病:过去三年
Kidney Int. 2009 Jul;76(2):149-68. doi: 10.1038/ki.2009.128. Epub 2009 May 20.
8
Advances in the pathogenesis and treatment of polycystic kidney disease.多囊肾病的发病机制与治疗进展
Curr Opin Nephrol Hypertens. 2009 Mar;18(2):99-106. doi: 10.1097/MNH.0b013e3283262ab0.
9
Neutrophil gelatinase-associated lipocalin suppresses cyst growth by Pkd1 null cells in vitro and in vivo.中性粒细胞明胶酶相关脂质运载蛋白在体外和体内均可抑制Pkd1基因敲除细胞的囊肿生长。
Kidney Int. 2008 Nov;74(10):1310-1318. doi: 10.1038/ki.2008.395. Epub 2008 Aug 13.
10
Polycystic kidney disease.多囊肾病
Annu Rev Med. 2009;60:321-37. doi: 10.1146/annurev.med.60.101707.125712.

巨噬细胞促进多囊肾病囊肿生长。

Macrophages promote cyst growth in polycystic kidney disease.

机构信息

Section of Nephrology, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.

出版信息

J Am Soc Nephrol. 2011 Oct;22(10):1809-14. doi: 10.1681/ASN.2011010084. Epub 2011 Sep 15.

DOI:10.1681/ASN.2011010084
PMID:21921140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3187181/
Abstract

Polycystic kidney disease (PKD) exhibits an inflammatory component, but the contribution of inflammation to cyst progression is unknown. Macrophages promote the proliferation of tubular cells following ischemic injury, suggesting that they may have a role in cystogenesis. Furthermore, cultured Pkd1-deficient cells express the macrophage chemoattractants Mcp1 and Cxcl16 and stimulate macrophage migration. Here, in orthologous models of both PKD1 and PKD2, abnormally large numbers of alternatively activated macrophages surrounded the cysts. To determine whether pericystic macrophages contribute to the proliferation of cyst-lining cells, we depleted phagocytic cells from Pkd1(fl/fl);Pkhd1-Cre mice by treating with liposomal clodronate from postnatal day 10 until day 24. Compared with vehicle-treated controls, macrophage-depleted mice had a significantly lower cystic index, reduced proliferation of cyst-lining cells, better-preserved renal parenchyma, and improved renal function. In conclusion, these data suggest that macrophages home to cystic areas and contribute to cyst growth. Interruption of these homing and proliferative signals could have therapeutic potential for PKD.

摘要

多囊肾病(PKD)表现出炎症成分,但炎症对囊肿进展的贡献尚不清楚。巨噬细胞在缺血性损伤后促进肾小管细胞的增殖,表明它们可能在囊肿发生中起作用。此外,培养的 Pkd1 缺陷细胞表达巨噬细胞趋化因子 Mcp1 和 Cxcl16 并刺激巨噬细胞迁移。在这里,在 PKD1 和 PKD2 的同源模型中,大量的交替激活的巨噬细胞包围着囊肿。为了确定囊周巨噬细胞是否有助于囊衬细胞的增殖,我们从出生后第 10 天至第 24 天用脂质体氯膦酸盐处理 Pkd1(fl/fl);Pkhd1-Cre 小鼠以耗尽吞噬细胞。与载体处理的对照组相比,巨噬细胞耗竭小鼠的囊泡指数明显降低,囊衬细胞增殖减少,肾实质保存更好,肾功能改善。总之,这些数据表明巨噬细胞归巢到囊性区域并促进囊肿生长。阻断这些归巢和增殖信号可能对 PKD 具有治疗潜力。