Gene Therapy for Neuropathic Pain through siRNA-IRF5 Gene Delivery with Homing Peptides to Microglia

• Published in: Molecular therapy. Nucleic acids Vol. 11; no. C; pp. 203 - 215
• Main Authors: Terashima, Tomoya, Ogawa, Nobuhiro, Nakae, Yuki, Sato, Toshiyuki, Katagi, Miwako, Okano, Junko, Maegawa, Hiroshi, Kojima, Hideto
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.06.2018; Elsevier Limited; American Society of Gene & Cell Therapy; Elsevier
• Subjects: astrocyte; Astrocytes; Conflicts of interest; Experiments; Funding; gene delivery; Gene therapy; Gene transfer; homing peptides; Hyperalgesia; Interferon; Interferon regulatory factor; interferon regulatory factor 5; IRF; Microglia; Neuralgia; Neurons; Pain; Pain perception; Pathogenesis; Peptides; Phage display; Plaques; siRNA; Spinal cord; Vectors (Biology); gene delivery; interferon regulatory factor 5; homing peptides; IRF; microglia; astrocyte
• ISSN: 2162-2531; 2162-2531
• DOI: 10.1016/j.omtn.2018.02.007

Astrocyte- and microglia-targeting peptides were identified and isolated using phage display technology. A series of procedures, including three cycles of both in vivo and in vitro biopanning, was performed separately in astrocytes and in M1 or M2 microglia, yielding 50–58 phage plaques in each cell type. Analyses of the sequences of this collection identified one candidate homing peptide targeting astrocytes (AS1[C-LNSSQPS-C]) and two candidate homing peptides targeting microglia (MG1[C-HHSSSAR-C] and MG2[C-NTGSPYE-C]). To determine peptide specificity for the target cell in vitro, each peptide was synthesized and introduced into the primary cultures of astrocytes or microglia. Those peptides could bind to the target cells and be selectively taken up by the corresponding cell, namely, astrocytes, M1 microglia, or M2 microglia. To confirm cell-specific gene delivery to M1 microglia, the complexes between peptide MG1 and siRNA-interferon regulatory factor 5 were prepared and intrathecally injected into a mouse model of neuropathic pain. The complexes successfully suppressed hyperalgesia with high efficiency in this neuropathic pain model. Here, we describe a novel gene therapy for the treatment neuropathic pain, which has a high potential to be of clinical relevance. This strategy will ensure the targeted delivery of therapeutic genes while minimizing side effects to non-target tissues or cells.