RGD Reference Report - Role of MKK3-p38 MAPK signalling in the development of type 2 diabetes and renal injury in obese db/db mice. - Rat Genome Database

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Role of MKK3-p38 MAPK signalling in the development of type 2 diabetes and renal injury in obese db/db mice.

Authors: Lim, AK  Nikolic-Paterson, DJ  Ma, FY  Ozols, E  Thomas, MC  Flavell, RA  Davis, RJ  Tesch, GH 
Citation: Lim AK, etal., Diabetologia. 2009 Feb;52(2):347-58. Epub 2008 Dec 9.
RGD ID: 2311566
Pubmed: PMID:19066844   (View Abstract at PubMed)
DOI: DOI:10.1007/s00125-008-1215-5   (Journal Full-text)

AIMS/HYPOTHESIS: Obesity and diabetes are associated with increased intracellular p38 mitogen-activated protein kinase (MAPK) signalling, which may promote tissue inflammation and injury. Activation of p38 MAPK can be induced by either of the immediate upstream kinases, MAP kinase kinase (MKK)3 or MKK6, and recent evidence suggests that MKK3 has non-redundant roles in the pathology attributed to p38 MAPK activation. Therefore, this study examined whether MKK3 signalling influences the development of obesity, type 2 diabetes and diabetic nephropathy. METHODS: Wild-type and Mkk3 (also known as Map2k3) gene-deficient db/db mice were assessed for the development of obesity, type 2 diabetes and renal injury from 8 to 32 weeks of age. RESULTS: Mkk3 (+/+) db/db and Mkk3 (-/-) db/db mice developed comparable obesity and were similar in terms of incidence and severity of type 2 diabetes. At 32 weeks, diabetic Mkk3 (+/+) db/db mice had increased kidney levels of phospho-p38 and MKK3 protein. In comparison, kidney levels of phospho-p38 in diabetic Mkk3 ( -/- ) db/db mice remained normal, despite a fourfold compensatory increase in MKK6 protein levels. The reduced levels of p38 MAPK signalling in the diabetic kidneys of Mkk3 ( -/- ) db/db mice was associated with protection against the following: declining renal function, increasing albuminuria, renal hypertrophy, podocyte loss, mesangial cell activation and glomerular fibrosis. Diabetic Mkk3 ( -/- ) db/db mice were also significantly protected from tubular injury and interstitial fibrosis, which was associated with reduced Ccl2 mRNA expression and interstitial macrophage accumulation. CONCLUSIONS/INTERPRETATION: MKK3-p38 MAPK signalling is not required for the development of obesity or type 2 diabetes, but plays a distinct pathogenic role in the progression of diabetic nephropathy in db/db mice.

RGD Manual Disease Annotations    Click to see Annotation Detail View
TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
Diabetic Nephropathies  ISOMapk14 (Mus musculus)2311566; 2311566associated with Diabetes Mellitus more ...RGD 
Diabetic Nephropathies  IEP 2311566associated with Diabetes Mellitus more ...RGD 

Objects Annotated

Genes (Rattus norvegicus)
Mapk14  (mitogen activated protein kinase 14)

Genes (Mus musculus)
Mapk14  (mitogen-activated protein kinase 14)

Genes (Homo sapiens)
MAPK14  (mitogen-activated protein kinase 14)


Additional Information