½Å »ç±¸Ã¼ Áúȯ¿¡¼ Nephrin, Glomerular Epithelial Cell Protein-1 [GLEPP1]
Altered Expression of Nephrin, Glomerular Epithelial Cell Protein-1, (GLEPP1) and WT-1 in Glomerular Disease
±èº´±Ç, ±èÁöÈÆ, ÀÌÇö¼ø,
¼Ò¼Ó »ó¼¼Á¤º¸
±èº´±Ç ( Kim Byoung-Kwon )
¼¿ï´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
±èÁöÈÆ ( Kim Ji-Hoon )
¼¿ï´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
ÀÌÇö¼ø ( Lee Hyun-Soon )
¼¿ï´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
KMID : 0357920020360010021
Abstract
Background: Glomerular epithelial cell protein-1 (GLEPP1)and WT-1 expressed in mature visceral glomerular epithelial cell(VGEC)is required for maintenance of the mature status of VGEC. Nephrin protein is located at the filtration slit and regarded as a molecular component of the slit diaphragm. Alterations of these proteins in proteinuric diseases are not clearlydefined.
Methods: We investigated the expression of GLEPP1, WT-1 and nephrin in 28 renal biopsies diagnosed with minimal change nephropathy (n=10), focal glomerulosclerosis(n=10) and membranous nephritis (n=8) by immunohistochemical staining. Normal control biopsies were obtained from six nephrectomy specimens.
Results: The patients consisted of 15 males and 13 females. The mean age was 40.7 years. Nephrotic range proteinuria (¡Ã3.5 g/day) was noted in 15(54%) patients. GLEPP1 and nephrin expression were significantly decreased in patients as compared with those of the controls (p£¼0.05). The mean number of WT-1 expressing cells per glomerulus was also significantly decreased in patients as compared with those of the controls (p£¼0.05). However, there was no significant difference in the number of WT-1 expressing cells among the disease groups.
Conclusions: These results suggest that the loss of biological markers of mature VGEC may play an important role in the pathogenesis of proteinuria.
Å°¿öµå
Nephrosis;Lipoid;Glomerulo Nephritis;Biological Markers
¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸
µîÀçÀú³Î Á¤º¸