Human Cord Blood CD133+ Stem Cells Transplanted to Nod-Scid Mice Provide Conditions for Regeneration of Olfactory Neuroepithelium After Permanent Damage Induced by Dichlobenil

Author:

Franceschini Valeria1,Bettini Simone1,Pifferi Simone2,Rosellini Alfredo3,Menini Anna2,Saccardi Ricardo4,Ognio Emanuela5,Jeffery Rosemary6,Poulsom Richard6,Revoltella Roberto P.3

Affiliation:

1. Department of Experimental Evolutionary Biology, University of Bologna, Bologna, Italy

2. Neurobiology Sector, International School for Advanced Studies S.I.S.S.A., Italian Institute of Technology, Trieste, Italy

3. National Research Council of Italy (CNR) and Foundation ONLUS “Stem Cells and Life,” Pisa, Italy

4. Department of Hematology, Bone Marrow Transplantation Center, University Hospital of Careggi, Firenze, Italy

5. Animal Model Facility, National Institute for Cancer Research (IST), Genova, Italy

6. Histopathology Laboratory, Cancer Research United Kingdom, London Research Institute, London, United Kingdom

Abstract

Abstract The herbicide dichlobenil selectively causes necrosis of the dorsomedial part of olfactory neuroepithelium (NE) with permanent damage to the underlying mucosa, whereas the lateral part of the olfactory region and the nasal respiratory mucosa remain undamaged. We investigated here whether human umbilical cord blood CD133+ stem cells (HSC) injected intravenously to nod-scid mice pretreated with dichlobenil may engraft the olfactory mucosa and contribute to the regeneration of the damaged NE. We tested HLA-DQα1 DNA and three human microsatellites (Combined DNA Index System) as indicators of engrafted cells, finding polymerase chain reaction evidence of chimaerism in various tissues of the host, including the olfactory mucosa and bulb, at 7 and 31 days following HSC transplantation. Histology, immunohistochemistry, and lectin staining revealed the morphological recovery of the dorsomedial region of the NE in dichlobenil-treated mice that received HSC, contrasting with the lack of regeneration in similarly injured areas as these remained damaged in control nontransplanted mice. FISH analysis, to detect human genomic sequences from different chromosomes, confirmed persistent engraftment of the regenerating olfactory area with chimeric cells. Electro-olfactograms in response to odorants, to test the functionality of the olfactory NE, confirmed the functional damage of the dorsomedial area in dichlobenil-treated mice and the functional recovery of the same area in transplanted mice. These findings support the concept that transplanted HSC migrating to the damaged olfactory area provide conditions facilitating the recovery from olfactory receptor cell loss. Disclosure of potential conflicts of interest is found at the end of this article.

Funder

Italian Ministry of University and Research

Cancer Research UK-London Research Institute

C.N.R., project RSTL 2007

Italian Ministry of Health and Istituto Zooprofilattico Sperimentale Lazio e Toscana

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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