Hydrogel nanoparticles covered by neuroligin-2-derived peptide-protected β cells under oxidative stress and increase their proliferation

Efrat Shtriker, Sharon Bretler, Anna Munder, Gerardo Byk, Guy Cohen, Michal Kolitz-Domb, Arie Gruzman

Research output: Contribution to journalArticlepeer-review


Protein complexes that mediate secretion and adhesion are located on the plasma membrane of pancreatic β cells. Neuroligins and their binding partners, the neurexins, are among these complexes. β cell maturation and physiologically regulated insulin secretion, as a response to high levels of blood glucose, are dependent on their three-dimensional (3D) arrangement. Both insulin secretion and the proliferation rates of β cells dramatically increase when β cells are co-cultured with clusters of a member of the neuroligin family: NL-2. A membranal protein, such as NL-2, has very limited drugability owing to its low biostability and bioavailability. Thus, based on in silico modeling, a short NL-2 peptide (HSA-28), which was able to mimic NL-2-positive effects on β cells, was designed, as we described in previous publication. However, the peptide was active only as a cluster, created by the covering the maghemite (γ-Fe2O3)-based nanoparticles (NPs) with limited biocompatibility. In this brief communication, we will show that conjugation of HSA-28 to biocompatible hydrogel NPs exhibits an impressive protective effect on INS-1E β cells under oxidative stress and induces their proliferation rate via augmentation of PDX1 nuclear translocation. The diameter of coated by the peptide NPs was 206 ± 63 nm (DLS) and 114 ± 27 nm (cryo-TEM). This significant change in size can be explained by the very hydrophilic character of the proteinoid NPs, inducing adsorption of many water molecules on their surface, which are accounted only by the DLS. The ability of biocompatible hydrogel NPs to prevent apoptosis and increase β cell mass might be used for developing novel β cell protective therapies. [Figure not available: see fulltext.].

Original languageEnglish
Article number221
JournalJournal of Nanoparticle Research
Issue number8
StatePublished - 1 Aug 2018

Bibliographical note

Funding Information:
Funding This study was supported by a Bar-Ilan University new faculty grant, a D-cure (Diabetes Care in Israel) Young Investigator Award, a NOFAR program (Israel Ministry of Industry), and The Israel Science Foundation (application number 117/2014) for A.G. G.C. is partially supported by Israel Ministry of Science and Technology.

Publisher Copyright:
© 2018, Springer Nature B.V.


  • Hydrogel nanoparticles
  • INS-1E β cells
  • Nanobiomedicine
  • Neuroligin-2
  • Oxidative stress
  • Peptide conjugation


Dive into the research topics of 'Hydrogel nanoparticles covered by neuroligin-2-derived peptide-protected β cells under oxidative stress and increase their proliferation'. Together they form a unique fingerprint.

Cite this