본문 바로가기
KERD
논문KCI 등재

배양한 사구체 상피세포에서 고농도 당과 후기 당화합물에 의한 P-cadherin의 변화

High Glucose and Advanced Glycosylation Endproducts(AGE) Modulate the P-cadherin Expression in Glomerular Epithelial Cells(GEpC)

1

조회

0

다운로드

2

인용

0

참고문헌

주제분류소아과학

초록

목 적:단백뇨 질환에서 볼 수 있는 사구체 상피세포(glomerular epithelial cells, GEpC) 족돌기 사이에 위치한 세극막(slit diaphragm)의 P-cadherin의 당뇨조건에 따른 병리학적 변화를 알아보고자 하였다. 방 법:백서 GEpC을 배양하고 고농도의 당과 후기당화합물(advanced glycosylation endproducts, AGE)을 적용하여 당뇨병 환경에 가까운 조건을 설정한 후, P-cadherin 단백양은 Western 분석으로, 유전자 표현의 변화는 RT-PCR로 관찰하였다. 실험군은 당의 농도를 5 또는 30 mM로, AGE와 BSA를 첨가하고 osmotic control로서 당 5 mM에 mannitol 25 mM을 섞은 것을 조합하여 A5, A30, B5, B30, Aosm로 하였다. 결 과:P-cadherin 단백양은 B5 결과를 대조군으로 비교하여 당을 첨가한 B30에서 50.4%의 감소, AGE를 추가한 조건인 A5와 A30에서 각각 7.4%와 30.4%의 의미 있는 감소를 보였다. 또한 P-cadherin mRNA의 표현은 B30에서 40.3%의 감소, A30에서 27.2%의 의의 있는 감소를 보였다. 이러한 감소 소견은 osmotic control(Aosm)에서는 관찰할 수 없었다. 결 론:고농도의 당과 AGE에 의한 GEpC의 P-cadherin을 유전자 수준에서의 억제로 단백의 생성 감소를 초래함으로써, 당뇨환경에서 세극막 성분의 변화를 설명할 수 있으며, 추후 이의 변화 기전에 대한 연구가 필요할 것으로 사료된다.

Abstract

Purpose : Podocytes are critical in maintaining the filtration barrier of the glomerulus and are dependent on the integrity of slit diaphragm(SD) proteins including nephrin, P-cadherin, and others. Diabetic proteinuric condition demonstrates defects in SD molecules as well as ultrastructural changes in podocytes. We examined the molecular basis for this alteration of SD molecules especially on P-cadherin as a candidate regulating the modulation of pathogenic changes in the barrier to protein filtration. Methods : To investigate whether high glucose and AGE induce changes in SD, we cultured rat GEpC under normal(5 mM) or high glucose(30 mM) and AGE- or BSA-added conditions and measured the change of P-cadherin expression by Western blotting and RT- PCR. Results : We found that administration of high glucose decreased the P-cadherin production significantly in the presence or absence of AGE by Western blotting. In RT-PCR high glucose with or without AGE also significantly decreased the expression of P-cadherin mRNA compared to those of controls. Such changes were not seen in the osmotic control. Conclusion : We suggest that high glucose with or without AGE suppresses the production of P-cadherin at the transcriptional level and that these changes may explain the functional changes of SD in diabetic conditions.

참고문헌 (39)

  1. Fauci AS,, "Pathogenetic mechanisms of glomerular injury. In : Brady HR, Brenner BM, editors. Harrison's Internal Medicine", pp.1534~6 (1998)
  2. Scandling J, "Glomerular size- selectivity and micro-albuminuria in early diabetic glomerular disease", 41, pp.840~6 (1992)
  3. Westberg NG, "Human glomerular basement membrane chemical composition in diabetes mellitus", 194, pp.39~47 (1973)
  4. Ha TS, "Researches on the pathophysiology of proteinuria in diabetic nephropathy", 41(1), pp.69~74 (1998)
  5. Sharma K, "Biochemical events and cytokine interactions linking glucose metabolism to the development of diabetic nephropathy", 17, pp.80~92 (1997)
  6. Vlassara H, "Protein glycation in the kidney:Role in diabetes and aging", 49, pp.1795~804 (1996)
  7. Tryggvason K, "Unraveling the mechanisms of glomerular ultrafiltration:nephrin,a key component of the slit diaphragm", 10, pp.2440~5 (1999)
  8. Reiser J, "The glomerular slit diaphragm is a modified adherens junction", 11, pp.1~8 (2000)
  9. Mundel P, "Podocyte biology and response to injury", 13, pp.3005~15 (2002)
  10. Asanuma K, "The role of podocytes in glomerular pathobiology", 7, pp.255~9 (2003)
  11. Ha TS, "Pathophysiology of Proteinuria", 47(4), pp.877~85 (2004)
  12. Shimoyama Y, "Cadherin cell adhesion molecules in human epithelial tissues and carcinomas", 49, pp.2128~33 (1989)
  13. Bains R, "A quantitative immunofluorescence study of glomerular cell adhesion proteins in proteinuric states", 183, pp.272~80 (1997)
  14. Singh AK, "Effect of glycated proteins on the matrix of glomerular epithelial cells", 9, pp.802~10 (1998)
  15. Xu ZG, "P-Cadherin is decreased in diabetic glomeruli and in glucose-stimulated podocytes in vivo and in vitro studies", 20, pp.524~31 (2005)
  16. Kreisberg JI, "Isolation and characterization of rat glomerular epithelial cells in vitro", 14, pp.21~30 (1978)
  17. Song CJ, "Effects of angiotensin II on glomerular epithelial cells permeability model;role of oxidative stress", 23, pp.396~404 (2004)
  18. Ha TS, "Effects of high glucose and advanced glycosylation endproducts on the α-actinin-4 expressed by glomerular epithelial cells", 23, pp.694~702 (2004)
  19. Ha TS, "Regulation of glomerular endothelial cell proteoglycans by glucose", 19, pp.245~52 (2004)
  20. Ha TS, "Effects of advanced glycation endproducts on rat glomerular epithelial cells:Roles of reactive oxygen species", 22, pp.285~93 (2003)
  21. Ha TS, "modulate the CD2AP expression in glomerular epithelial cells", 24 (2005)
  22. Ha TS, "Effects of high glucose and advanced glycosylation endproducts on the ZO-1 expression in glomerular epithelial cells", 8, pp.138~48 (2004)
  23. Chugh SS, "Molecular structure-function relationship in the slit diaphragm", 23, pp.544~55 (2003)
  24. Oh J, "Dynamic(re)organization of the podocyte actin cytoskeleton in the nephrotic syndrome", 19, pp.130~7 (2004)
  25. Rodewald R, "Porous substructure of the glomerular slit diaphragm in the rat and mouse", 60, pp.423~33 (1974)
  26. Schnabel E, "The tight junction protein ZO-1 is concentrated along slit diaphragms of the glomerular epithelium", 111, pp.1255~63 (1990)
  27. Dreyer SD, "LMX1B transactivation and expression in nail-patella syndrome", 9, pp.1067~74 (2000)
  28. Tryggvason K, "Molecular basis of glomerular permselectivity", 10, pp.543~9 (2001)
  29. Grunwald GB, "The structural and functional analysis of cadherin calcium-dependent cell adhesion molecules", 5, pp.797~805 (1993), Curr Opin Cell Biol
  30. Vleminckx K, "Genetic manipulation of E- cadherin expression by epithelial tumour cells reveals an invasion suppressor role", 66, pp.107~19 (1991)
  31. Geiger B, "Cadherins", 8, pp.307~32 (1992)
  32. Goodwin M, "Classical cadherin adhesion molecules : coordinating cell adhesion, signaling and the cytoskeleton J Mol Histol", 35, pp.839~44 (2004)
  33. Yaoita E,, "Cadherin and catenin staining in podocytes in development and puromycin aminonucleoside nephrosis Nephrol Dial Transplant", 17(9), pp.9 16~9 (2002)
  34. Goto S, "Involvement of R-cadherin in the early stage of glomerulogenesis", 9, pp.1234~41 (1998)
  35. Nakopoulou L, "Evaluation of E-cadherin", catenin complex in primary and secondary glomerulonephritis, 2002, pp.39, 469~74
  36. Ruotsalainen V, "Role of nephrin in cell junction formation in human nephrogenesis", 157, pp.1905~16 (2000)
  37. Radice GL, "Precocious mammary gland development in P-cadherin-deficient mice", 139, pp.1025~32 (1997)
  38. Otero K, "Albumin- derived advanced glycation end-products trigger the disruption of the vascular endothelial cadherin complex in cultured human and murine endothelial cells", 359, pp.567~74 (2001)
  39. Ha TS, "Effects of high glucose and advanced glycosylation endproducts on the in vitro permeability model using semipermeable membrane", 12, pp.835~ (2001)

관련 논문AI추천

이 간행물의 다른 논문 (20건)