Survival of retinal ganglion cells in slice culture provides a rapid screen for olfactory ensheathing cell preparations (original) (raw)

Transplanted olfactory ensheathing cells promote regeneration of cut adult rat optic nerve axons

The Journal of neuroscience : the official journal of the Society for Neuroscience, 2003

Transplantation of olfactory ensheathing cells into spinal cord lesions promotes regeneration of cut axons into terminal fields and functional recovery. This repair involves the formation of a peripheral nerve-like bridge in which perineurial-like fibroblasts are organized into a longitudinal stack of parallel tubular channels, some of which contain regenerating axons enwrapped by Schwann-like olfactory ensheathing cells. The present study examines whether cut retinal ganglion cell axons will also respond to these cells, and if so, whether they form the same type of arrangement. In adult rats, the optic nerve was completely severed behind the optic disc, and a matrix containing cultured olfactory ensheathing cells was inserted between the proximal and distal stumps. After 6 months, the transplanted cells had migrated for up to 10 mm into the distal stump. Anterograde labeling with cholera toxin B showed that cut retinal ganglion cell axons had regenerated through the transplants, en...

Ensheathing cell cultures from the olfactory bulb and mucosa

Glia, 2004

Transplantation of cells cultured from the nerve layers of the adult rat olfactory bulb has been shown to repair CNS tract injuries. The precise cellular composition of the culture appears to be important for this effect. Comparison was made of tissue cultured from the adult rat olfactory mucosa with that from the olfactory bulb. Both yielded mixtures of p75 immunoreactive cells and fibronectin immunoreactive cells. In sequential observations over 21 days in culture, the population of p75-expressing cells was maintained and continued to proliferate for longer in the samples from the olfactory mucosa. For derivation of cells for transplantation, the mucosa can be accessed without the need for intracranial surgery.

New method of purification for establishing primary cultures of ensheathing cells from the adult olfactory bulb

Glia, 2001

Ensheathing cells exclusively enfold olfactory axons. The ability of olfactory axons to reinnervate the adult mammalian olfactory bulb throughout the lifetime of an organism is believed to result from the presence of this unique glial cell in the olfactory system. This theory has been substantiated by research demonstrating the ability of transplanted ensheathing cells to promote axonal regrowth in areas of the central nervous system that are normally nonpermissive. A simple method for purifying ensheathing cells resulting in a large yield of cells is therefore invaluable for transplantation studies. We have developed such a method based on the differing rates of attachment of the various harvested cell types. The greatest percentage of cells (70.4%) that attached during the first step of the separation was determined to be fibroblasts. The remainder of the cells were classified as astrocytes (20.8%) and ensheathing cells (6.8%). The percentage of attached astrocytes (67.6%) was greatly increased during the second purification step while the percentage of fibroblasts decreased greatly (27.9%) and the percentage of ensheathing cells (5.3%) slightly decreased. In the final cultures, 93.2 % of the attached cells were ensheathing cells, while astrocytes (5.9%) and fibroblasts (1.4%) were only minor components. This simple, inexpensive method of purifying ensheathing cells will facilitate their use in central nervous system regeneration research. GLIA 34:81-87,

In vitro Maintenance of Olfactory Mucosa: with Enriched Olfactory Ensheathing Cells

Journal of Stem Cell Research & Therapy, 2013

Human Olfactory Mucosa (OM) regulates olfaction through axonal regeneration and myelination mediated by stem cells and Olfactory Ensheathing Cells (OECs) resident in the niche. Purified OECs/olfactory biopsies have been utilized for functional recovery in different Spinal Cord Injury (SCI) models. However, recent reports find this debatable where we propose primary culture of OM, basal cells of olfactory epithelium and olfactory ecto-mesenchymal stem cells. Our defined culture conditions improve the life span of OM with enrichment of OECs providing a strategy for employment for SCI/cochlear damage repair. Briefly, OM post-collection, was non-enzymatically sliced, cultured for 6 weeks and cells characterized morphologically, immuno-cytochemically and western blotting. By day 21, ~70% GFAP and p75NTR stained, spindle shaped astrocyte-like and flattened sheet-like OECs displayed axonal remyelination. By day 30, caspase 3, 8, 9 (gene-product and activity), phospho-p53 negative; GFAP and p75NTR positive dense, overlapping mass of cells was found. This was accompanied with degenerative changes by 6 weeks through GFAP staining. Conversely, trypsination on day 21 resulted in >95% OECs with flattened morphology, GFAP and p75NTR positivity. The human derived OECs were compared with the 2-day SD rat Olfactory Bulb Cells cultured for 2 weeks in F12 media (GFAP and p75NTR positive). Hence, cultured olfactory mucosa displaying axonal regeneration with OECs in culture provides a vehicle for SCI/cochlear damage repair studies.

The role of olfactory ensheating cells in regenerative medicine: review of the literature

Romanian Journal of Rhinology, 2015

Olfactory ensheathing cells (OECs) join olfactory axons in their entrance to the central nervous system, representing a unique population of glial cells with functions in olfactory neurogenesis, axonal growth and olfactory bulb formation. Olfactory ensheathing cells have a great potential to induce repair for neural injuries, in central nervous system and peripheral nervous system, existing numerous experimental and clinical studies lately, reporting beneficial effects in anatomical and functional recovery. Studies are also conducted in order to establish possible pro-regenerative effects of the OECs, their potential in tissue repair and ability to modulate the immune system. The aim of this paper was to review the properties of olfactory ensheathing cells and their potential therapeutic role in regenerative medicine.

Death of Axotomized Retinal Ganglion Cells Delayed After Intraoptic Nerve Transplantation of Olfactory Ensheathing Cells in Adult Rats

Cell Transplantation, 2010

Intraorbital transection of the optic nerve (ON) always induces ultimate apoptosis of retinal ganglion cells (RGCs) and consequently irreversible defects of vision function. It was demonstrated that transplanted olfactory ensheathing cells (OECs) in partially injured spinal cord have a distant in vivo neuroprotective effect on descending cortical and brain stem neurons. However, this study gave no answers to the question whether OECs can protect the central sensitive neurons with a closer axonal injury because different neurons respond variously to similar axonal injury and the distance between the neuronal soma and axonal injury site has a definite effect on the severity of neuronal response and apoptosis. In the present study, we investigated the effect of transplanted OECs on RGCs after intraorbital ON transection in adult rats. Green fluorescent protein (GFP)-OECs were injected into the ocular stumps of transected ON and a significantly higher number of surviving RGCs was found ...

Morphological and functional plasticity of olfactory ensheathing cells

Journal of Neurocytology, 2005

In the primary olfactory pathway, olfactory ensheathing cells (OECs) extend processes to envelop bundles of olfactory axons as they course towards their termination in the olfactory bulb. The expression of growth-promoting adhesion and extracellular matrix molecules by OECs, and their spatially close association with olfactory axons are consistent with OECs being involved in promoting and guiding olfactory axon growth. Because of this, OECs have been employed as a possible tool for inducing axonal regeneration in the injured adult CNS, resulting in significant functional recovery in some animal models and promising outcomes from early clinical applications. However, fundamental aspects of OEC biology remain unclear. This brief review discusses some of the experimental data that have resulted in conflicting views with regard to the identity of OECs. We present here recent findings which support the notion of OECs as a single but malleable phenotype which demonstrate extensive morphological and functional plasticity depending on the environmental stimuli. The review includes a discussion of the normal functional role of OECs in the developing primary olfactory pathway as well as their interaction with regenerating axons and reactive astrocytes in the novel environment of the injured CNS. The use of OECs to induce repair in the injured nervous system reflects the functional plasticity of these cells. Finally, we will explore the possibility that recent microarray data could point to OECs assuming an innate immune function or playing a role in modulating neuroinflammation.

A Novel Approach for Mucosal and Bulbar Olfactory Ensheathing Cell Isolation Based on the Non-Adherent Subculture Technique

Basic and clinical neuroscience, 2022

Olfactory ensheathing cells (OECs) are widely used in transplantation studies. Therefore, the high purification of this unique cell type will be valuable for medical applications. Although recent improvements in OEC isolation procedures opened a new era in this field, the high purification efficacy and viability rate are still needed to be considered. The most widely used OECs isolation techniques can be broadly classified as based on adherence properties in particular in the case of olfactory bulbderived OECs isolation. Considering the invasive nature of harvesting OECs from human olfactory bulbs, hence the high efficient purification of these cells from olfactory mucosa can be beneficial in clinical trials. In this study, we isolated OECs from both the olfactory bulb and mucosa of rats due to their differential adherence properties and compared them. Cell preparations were characterized by NGFR p75 and S100β antibodies, the specific markers for OECs using immunocytochemistry and western blot analysis respectively. OECs morphology and viability were monitored over time by microscopy and MTT assay. We found that utilizing our suggested method, OECs could be purified from the olfactory mucosa as efficiently as the olfactory bulb. Both sources-derived OECs showed high levels of NGFR p75 and S100β expression, although the S100β expression was higher in olfactory mucosa-derived OECs preparations (P<0.05). Moreover, there was no significant difference between the two sources in cell viability in our suggested protocol. Hence due to the non-invasive harvesting method, olfactory mucosa-derived OECs are preferred from a clinical point of view for transplantation studies.