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. 2020 Jun 9;21(11):4113. doi: 10.3390/ijms21114113

Table 1.

Aberrant DNA-methylation in diabetic nephropathy (DN) and cells cultured under high glucose (HG) conditions.

Change in DN * Effect in Target Gene ** Model Cell or Tissue Reference
↓ DNA-methylation MIOX STZ mice Kidney [64]
HG in human cells Tubular (HK-2)
MMP9 HG in human cells Podocytes [66]
CLDN-1 STZ mice Kidney [69]
HG in human cells Renal epithelial cells
CTGF HG in human cells Mesangial cells [70]
TGFB1 db/db mice Mesangial cells from diabetic mice [74,75]
db/db mice Kidney
HG in human cells Mesangial cells
Agt, Abcc4, Slco1a1 db/db mice Proximal tubules [63]
↑ DNA-methylation ↓ mTOR upstream inhibitors db/db mice Immune cells from diabetic mice [81]
NPHS1 db/db mice Kidney [67,68]
STZ and db/db mice Kidney and isolated podocytes
HG in human cells Podocytes
Trim13 STZ and db/db mice Kidney [71]
KLF4 TGF-β1 in human cells HK-2 [79]
RCAN1 HG in human cells Podocytes [80]
Rasal1 STZ mice Kidney [82]
ESX1, GRIA3 HG in human cells Podocytes [65]

Streptozotocin (STZ) induces insulin-deficient diabetes that resembles type 1 DM, although there is no autoimmune component, while db/db mice are a model for type 2 DM. * Downward looking arrows mean decreased DNA-methylation and upward looking arrows mean increased DNA-methylation. ** Upward looking arrows mean increased gene expression and downward looking arrows mean decreased gene expression.