Transplantation of olfactory ensheathing cells to evaluate functional recovery after peripheral nerve injury

• Published in: Journal of visualized experiments 2014-02 (84), p.e50590-e50590
• Main Authors: Guerout, Nicolas, Paviot, Alexandre, Bon-Mardion, Nicolas, Honoré, Axel, Obongo, Rais, Duclos, Célia, Marie, Jean-Paul
• Format: Article
• Language: English
• Subjects: Anastomosis, Surgical; Animals; Cell Culture Techniques - methods; Cell Transplantation - methods; Laryngeal Nerve Injuries - physiopathology; Laryngeal Nerve Injuries - surgery; Larynx - physiopathology; Neuroscience; Olfactory Bulb - cytology; Olfactory Mucosa - cytology; Rats
• ISSN: 1940-087X; 1940-087X
• DOI: 10.3791/50590

Olfactory ensheathing cells (OECs) are neural crest cells which allow growth and regrowth of the primary olfactory neurons. Indeed, the primary olfactory system is characterized by its ability to give rise to new neurons even in adult animals. This particular ability is partly due to the presence of OECs which create a favorable microenvironment for neurogenesis. This property of OECs has been used for cellular transplantation such as in spinal cord injury models. Although the peripheral nervous system has a greater capacity to regenerate after nerve injury than the central nervous system, complete sections induce misrouting during axonal regrowth in particular after facial of laryngeal nerve transection. Specifically, full sectioning of the recurrent laryngeal nerve (RLN) induces aberrant axonal regrowth resulting in synkinesis of the vocal cords. In this specific model, we showed that OECs transplantation efficiently increases axonal regrowth. OECs are constituted of several subpopulations present in both the olfactory mucosa (OM-OECs) and the olfactory bulbs (OB-OECs). We present here a model of cellular transplantation based on the use of these different subpopulations of OECs in a RLN injury model. Using this paradigm, primary cultures of OB-OECs and OM-OECs were transplanted in Matrigel after section and anastomosis of the RLN. Two months after surgery, we evaluated transplanted animals by complementary analyses based on videolaryngoscopy, electromyography (EMG), and histological studies. First, videolaryngoscopy allowed us to evaluate laryngeal functions, in particular muscular cocontractions phenomena. Then, EMG analyses demonstrated richness and synchronization of muscular activities. Finally, histological studies based on toluidine blue staining allowed the quantification of the number and profile of myelinated fibers. All together, we describe here how to isolate, culture, identify and transplant OECs from OM and OB after RLN section-anastomosis and how to evaluate and analyze the efficiency of these transplanted cells on axonal regrowth and laryngeal functions.