4.7 Article

Multifunctional Natural Polymer Nanoparticles as Antifibrotic Gene Carriers for CKD Therapy

Journal

JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
Volume 31, Issue 10, Pages 2292-2311

Publisher

AMER SOC NEPHROLOGY
DOI: 10.1681/ASN.2019111160

Keywords

chronic kidney disease; fibrosis; nanoparticles; gene therapy; regenerative medicine

Funding

  1. National Natural Science Foundation of China (NSFC) International Young Scholar Research Fellowship [81850410552]
  2. NSFC Key National Project Fund [81830060]
  3. NSFC [81701840]
  4. Open Funding of the State Key Laboratory of Kidney Diseases [KF-2018-10]
  5. National Key Research and Development Program of China [2016YFA0101002]

Ask authors/readers for more resources

Background Progressive fibrosis is the underlying pathophysiological process of CKD, and targeted prevention or reversal of the profibrotic cell phenotype is an important goal in developing therapeutics for CKD. Nanoparticles offer new ways to deliver antifibrotic therapies to damaged tissues and resident cells to limit manifestation of the profibrotic phenotype. Methods We focused on delivering plasmid DNA expressing bone morphogenetic protein 7 ( BMP7) or hepatocyte growth factor (HGF)-NK1 (HGF/NK1) by encapsulation within chitosan nanoparticles coated with hyaluronan, to safely administer multifunctional nanoparticles containing the plasmid DNA to the kidneys for localized and sustained expression of antifibrotic factors. We characterized and evaluated nanoparticles in vitro for biocompatibility and antifibrotic function. To assess antifibrotic activity in vivo, we used noninvasive delivery to unilateral ureteral obstruction mouse models of CKD. Results Synthesis of hyaluronan-coated chitosan nanoparticles containing plasmid DNA expressing either BMP7 or NGF/NKI resulted in consistently sized nanoparticles, which-following endocytosis driven by CD441 cells-promoted cellular growth and inhibited fibrotic gene expression in vitro. Intravenous tail injection of these nanoparticles resulted in approximately 40%-45% of gene uptake in kidneys in vivo. The nanoparticles attenuated the development of fibrosis and rescued renal function in unilateral ureteral obstructionmousemodels ofCKD. Gene delivery ofBMP7 reversed the progression of fibrosis and regenerated tubules, whereas delivery of HGF/NK1 halted CKD progression by eliminating collagen fiber deposition. Conclusions Nanoparticle delivery of HGF/NK1 conveyed potent antifibrotic and proregenerative effects. Overall, this research provided the proof of concept on which to base future investigations for enhanced targeting and transfection of therapeutic genes to kidney tissues, and an avenue toward treatment of CKD.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available