4.6 Article

Intranasal Delivery of Neural Stem/Progenitor Cells: A Noninvasive Passage to Target Intracerebral Glioma

Journal

STEM CELLS TRANSLATIONAL MEDICINE
Volume 1, Issue 12, Pages 866-873

Publisher

ALPHAMED PRESS
DOI: 10.5966/sctm.2012-0045

Keywords

Cell transplantation; Clinical translation; Neural stem cell; Glioma

Funding

  1. Deutsche Forschungsgemeinschaft [Schm 1631/3-1, SE 2052/1-1]
  2. Hamburger Krebshilfe e.V.
  3. Stiftung zur Bekampfung neuroviraler Erkrankungen

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Stem cell-based therapies for neurological disorders, including brain tumors, advance continuously toward clinical trials. Optimized cell delivery to the central nervous system remains a challenge since direct intracerebral injection is an invasive method with low transplantation efficiency. We investigated the feasibility of intranasal administration of neural stem/progenitor cells (NSPCs) as an alternative, noninvasive, and direct passage for the delivery of stem cells to target malignant gliomas. Tumor-targeting and migratory pathways of murine and human NSPCs were investigated by intravital magnetic resonance imaging and in histological time course analyses in the intracerebral U87, NCE-G55T2, and syngenic GI261 glioblastoma models. Intranasally administered NSPCs displayed a rapid, targeted tumor tropism with significant numbers of NSPCs accumulating specifically at the intracerebral glioma site within 6 hours after intranasal delivery. Histological time series analysis revealed that NSPCs migrated within the first 24 hours mainly via olfactory pathways but also by systemic distribution via the microvasculature of the nasal mucosa. Intranasal application of NSPCs leads to a rapid, targeted migration of cells toward intracerebral gliomas. The directional distribution of cells accumulating intra- and peritumorally makes the intranasal delivery of NSPCs a promising noninvasive and convenient alternative delivery method for the treatment of malignant gliomas with the possibility of multiple dosing regimens. STEM CELLS TRANSLATIONAL MEDICINE 2012;1:866-873

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