The Protective Effects of Neurotrophins and MicroRNA in Diabetic Retinopathy, Nephropathy and Heart Failure via Regulating Endothelial Function

Biomolecules. 2022 Aug 12;12(8):1113. doi: 10.3390/biom12081113.

Abstract

Diabetes mellitus is a common disease affecting more than 537 million adults worldwide. The microvascular complications that occur during the course of the disease are widespread and affect a variety of organ systems in the body. Diabetic retinopathy is one of the most common long-term complications, which include, amongst others, endothelial dysfunction, and thus, alterations in the blood-retinal barrier (BRB). This particularly restrictive physiological barrier is important for maintaining the neuroretina as a privileged site in the body by controlling the inflow and outflow of fluid, nutrients, metabolic end products, ions, and proteins. In addition, people with diabetic retinopathy (DR) have been shown to be at increased risk for systemic vascular complications, including subclinical and clinical stroke, coronary heart disease, heart failure, and nephropathy. DR is, therefore, considered an independent predictor of heart failure. In the present review, the effects of diabetes on the retina, heart, and kidneys are described. In addition, a putative common microRNA signature in diabetic retinopathy, nephropathy, and heart failure is discussed, which may be used in the future as a biomarker to better monitor disease progression. Finally, the use of miRNA, targeted neurotrophin delivery, and nanoparticles as novel therapeutic strategies is highlighted.

Keywords: diabetes mellitus; diabetic nephropathy; diabetic retinopathy; heart failure; microRNA; microvascular complications; neurotrophins.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Blood-Retinal Barrier / metabolism
  • Diabetes Mellitus* / metabolism
  • Diabetic Retinopathy* / metabolism
  • Heart Failure* / metabolism
  • Humans
  • Kidney Diseases* / metabolism
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Nerve Growth Factors

Substances

  • MicroRNAs
  • Nerve Growth Factors

Grants and funding

This work was supported by the DFG grant Fo 315/5-1 to C.Y.F., the DFG grant BR 4957/3-1 and to B.M.B., and grant from foundation Forschung hilft to C.Y.F.