Glomerular Endothelial Cell Injury and Focal Segmental Glomerulosclerosis Lesion in Idiopathic Membranous Nephropathy

被引:27
作者
Morita, Megumi [1 ]
Mii, Akiko [1 ]
Shimizu, Akira [2 ]
Yasuda, Fumihiko [1 ]
Shoji, Jun [3 ]
Masuda, Yukinari [2 ]
Ohashi, Ryuji [4 ]
Nagahama, Kiyotaka [2 ]
Kaneko, Tomohiro [1 ]
Tsuruoka, Shuichi [1 ]
机构
[1] Nippon Med Sch, Dept Nephrol, Tokyo 113, Japan
[2] Nippon Med Sch, Dept Analyt Human Pathol, Tokyo 113, Japan
[3] George Washington Univ, Dept Neurol, Washington, DC 20037 USA
[4] Nippon Med Sch, Div Diagnost Pathol, Tokyo 113, Japan
关键词
GROWTH-FACTOR; NEPHROTIC SYNDROME; PROGNOSTIC-FACTORS; VEGF INHIBITION; EXPRESSION; GLOMERULONEPHRITIS; HYPERTROPHY; PODOCYTES; URINE;
D O I
10.1371/journal.pone.0116700
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Focal segmental glomerulosclerosis (FSGS) lesions have often been discussed as a negative predictor in idopathic membranous nephropathy (MN). The mechanism of the development of FSGS lesion in MN is still uncertain. Methods From 250 cases of MN, 26 cases contained FSGS lesion. We compared the clinicopathological characteristics between MN cases with FSGS lesion [MN-FSGS(+)] and MN without FSGS lesion [MN-FSGS(-)], matched for gender, age, stage of MN. Results The glomerular filtration rate (eGFR) was significantly lower in MN-FSGS(+) cases compared to MN-FSGS(-), although nephrotic syndrome, hematuria, and systolic blood pressure levels were not significantly different between the two groups. Pathologically, glomeruli in MN-FSGS(+) cases showed narrowing and loss of glomerular capillaries with separating from GBM or disappearance of CD34+ endothelial cells, and accumulation of extracellular matrix (ECM) in capillary walls, indicating the development of glomerular capillary injury. These findings of endothelial injury were seen even in MN-FSGS(-) cases, but they were more prominent in MN-FSGS(+) than MN-FSGS(-) by computer assessed morphometric analysis. In MN-FSGS(+) cases, 44 out of 534 glomeruli (8.2%) contained FSGS lesions (n = 31, NOS lesion; n = 13, perihilar lesion). Significant thickness of GBM with ECM accumulation was evident in MN-FSGS(+) cases. Podocyte injury with effacement of foot processes was also noted, but the expression of VEGF on podocytes was not different between the two groups, which suggests that the significant thickness of capillary walls may influence the function of VEGF from podocyte resulting in the glomerular capillary injury that contribute to the development of FSGS lesion in MN. Conclusion Glomerular capillary injury was seen in all MN cases. Furthermore, the prominent injuries of glomerular capillaries may be associated with the deterioration of eGFR and the formation of FSGS lesions in MN.
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