Suppr超能文献

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.

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。

相似文献

1
Macrophages promote cyst growth in polycystic kidney disease.巨噬细胞促进多囊肾病囊肿生长。
J Am Soc Nephrol. 2011 Oct;22(10):1809-14. doi: 10.1681/ASN.2011010084. Epub 2011 Sep 15.
5
Macrophages promote polycystic kidney disease progression.巨噬细胞促进多囊肾病的进展。
Kidney Int. 2013 May;83(5):855-64. doi: 10.1038/ki.2012.446. Epub 2013 Feb 20.

引用本文的文献

6
Physiologic mechanisms underlying polycystic kidney disease.多囊肾病的生理机制。
Physiol Rev. 2025 Jul 1;105(3):1553-1607. doi: 10.1152/physrev.00018.2024. Epub 2025 Feb 12.
7
The impact of maternal obesity on polycystic kidney disease progression in a mouse model.母体肥胖对小鼠模型中多囊肾病进展的影响。
Am J Physiol Renal Physiol. 2025 Mar 1;328(3):F316-F327. doi: 10.1152/ajprenal.00227.2024. Epub 2025 Feb 5.
9
Intestinal barrier function declines during polycystic kidney disease progression.在多囊肾病进展过程中,肠道屏障功能会下降。
Am J Physiol Renal Physiol. 2025 Feb 1;328(2):F218-F229. doi: 10.1152/ajprenal.00058.2024. Epub 2024 Dec 18.
10
Adamts1 and Cyst Expansion in Polycystic Kidney Disease.Adamts1与多囊肾病中的囊肿扩张
J Am Soc Nephrol. 2025 Apr 1;36(4):559-570. doi: 10.1681/ASN.0000000557. Epub 2024 Nov 8.

本文引用的文献

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.
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.
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.
10
Polycystic kidney disease.多囊肾病
Annu Rev Med. 2009;60:321-37. doi: 10.1146/annurev.med.60.101707.125712.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验