Unknown

Dataset Information

0

Endogenous miR-204 Protects the Kidney against Chronic Injury in Hypertension and Diabetes.


ABSTRACT:

Background

Aberrant microRNA (miRNA) expression affects biologic processes and downstream genes that are crucial to CKD initiation or progression. The miRNA miR-204-5p is highly expressed in the kidney but whether miR-204-5p plays any role in the development of chronic renal injury is unknown.

Methods

We used real-time PCR to determine levels of miR-204 in human kidney biopsies and animal models. We generated Mir204 knockout mice and used locked nucleic acid-modified anti-miR to knock down miR-204-5p in mice and rats. We used a number of physiologic, histologic, and molecular techniques to analyze the potential role of miR-204-5p in three models of renal injury.

Results

Kidneys of patients with hypertension, hypertensive nephrosclerosis, or diabetic nephropathy exhibited a significant decrease in miR-204-5p compared with controls. Dahl salt-sensitive rats displayed lower levels of renal miR-204-5p compared with partially protected congenic SS.13BN26 rats. Administering anti-miR-204-5p to SS.13BN26 rats exacerbated interlobular artery thickening and renal interstitial fibrosis. In a mouse model of hypertensive renal injury induced by uninephrectomy, angiotensin II, and a high-salt diet, Mir204 gene knockout significantly exacerbated albuminuria, renal interstitial fibrosis, and interlobular artery thickening, despite attenuation of hypertension. In diabetic db/db mice, administering anti-miR-204-5p exacerbated albuminuria and cortical fibrosis without influencing blood glucose levels. In all three models, inhibiting miR-204-5p or deleting Mir204 led to upregulation of protein tyrosine phosphatase SHP2, a target gene of miR-204-5p, and increased phosphorylation of signal transducer and activator of transcription 3, or STAT3, which is an injury-promoting effector of SHP2.

Conclusions

These findings indicate that the highly expressed miR-204-5p plays a prominent role in safeguarding the kidneys against common causes of chronic renal injury.

SUBMITTER: Cheng Y 

PROVIDER: S-EPMC7350998 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC6339564 | biostudies-literature
| S-EPMC10277925 | biostudies-literature
| S-EPMC3507365 | biostudies-literature
| S-EPMC7396439 | biostudies-literature
| S-EPMC2689910 | biostudies-literature
| S-EPMC3354618 | biostudies-literature
| S-EPMC2900964 | biostudies-literature
| S-EPMC3612389 | biostudies-literature
| S-EPMC3491167 | biostudies-literature
| S-EPMC4588407 | biostudies-literature