Prevention of Diabetes-Induced Microangiopathy by Human Tissue Kallikrein Gene Transfer

Author:

Emanueli Costanza1,Salis Maria B.1,Pinna Alessandra1,Stacca Tiziana1,Milia Anna F.1,Spano Alessandra1,Chao Julie1,Chao Lee1,Sciola Luigi1,Madeddu Paolo1

Affiliation:

1. From Cardiovascular Medicine and Gene Therapy Section, National Laboratory of the National Institute of Biostructures and Biosystems (INBB) (C.E., M.B.S., A.P., T.S., A.F.M., A.S., P.M.), Osilo, Italy; Internal Medicine (P.M.) and Physiological, Biochemical and Cellular Sciences (A.S., L.S.), University of Sassari, Sassari, Italy; and Department of Biochemistry and Molecular Biology (J.C, L.C.), Medical University of South Carolina, Charleston, SC.

Abstract

Background— Microvascular insufficiency represents a major cause of end-organ failure among diabetics. Methods and Results— In streptozotocin-induced diabetic mice, we evaluated the potential of human tissue kallikrein (hTK) gene as a sole therapy against peripheral microangiopathy. Local delivery of hTK gene halted the progression of microvascular rarefaction in hindlimb skeletal muscle by inhibiting apoptosis, thus ensuring an improved hemodynamic recovery in case of supervening vascular occlusion. The curative action of hTK did not necessitate insulin supplementation. Application of gene therapy at a stage of established microangiopathy stimulated vascular regeneration. Conclusions— Our studies indicate that hTK may represent a useful tool for the treatment of microvascular complications in diabetics.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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