Single-cell printing to form three-dimensional lines of olfactory ensheathing cells

Biological laser printing (BioLP) is a unique tool capable of printing high resolution two- and three-dimensional patterns of living mammalian cells, with greater than 95% viability. These results have been extended to primary cultured olfactory ensheathing cells (OECs), harvested from adult Sprague-Dawley rats. OECs have been found to provide stimulating environments for neurite outgrowth in spinal cord injury models. BioLP is unique in that small load volumes ( approximately microLs) are required to achieve printing, enabling low numbers of OECs to be harvested, concentrated and printed. BioLP was used to form several 8 mm lines of OECs throughout a multilayer hydrogel scaffold. The line width was as low as 20 microm, with most lines comprising aligned single cells. Fluorescent confocal microscopy was used to determine the functionality of the printed OECs, to monitor interactions between printed OECs, and to determine the extent of cell migration throughout the 3D scaffold. High-resolution printing of low cell count, harvested OECs is an important advancement for in vitro study of cell interactions and functionality. In addition, these cell-printed scaffolds may provide an alternative for spinal cord repair studies, as the single-cell patterns formed here are on relevant size scales for neurite outgrowth.

[1]  G. Raisman,et al.  Transplantation of Olfactory Ensheathing Cells into Spinal Cord Lesions Restores Breathing and Climbing , 2003, The Journal of Neuroscience.

[2]  B. R. Ringeisen,et al.  Cell patterning without chemical surface modification: Cell-cell interactions between printed bovine aortic endothelial cells (BAEC) on a homogeneous cell-adherent hydrogel , 2006 .

[3]  R. Cortesini,et al.  Stem cells, tissue engineering and organogenesis in transplantation. , 2005, Transplant immunology.

[4]  L. Liotta,et al.  Isolation and characterization of type IV procollagen, laminin, and heparan sulfate proteoglycan from the EHS sarcoma. , 1982, Biochemistry.

[5]  B R Ringeisen,et al.  Printing of protein microarrays via a capillary‐free fluid jetting mechanism , 2005, Proteomics.

[6]  T. Kosaka,et al.  How simple is the organization of the olfactory glomerulus?: the heterogeneity of so-called periglomerular cells , 1998, Neuroscience Research.

[7]  F. Valverde,et al.  Olfactory bulb ensheathing glia: A unique cell type with axonal growth‐promoting properties , 1995, Glia.

[8]  D J Williams,et al.  Tissue engineering and regenerative medicine: manufacturing challenges. , 2005, IEE proceedings. Nanobiotechnology.

[9]  G W Plant,et al.  Long-Distance Axonal Regeneration in the Transected Adult Rat Spinal Cord Is Promoted by Olfactory Ensheathing Glia Transplants , 1998, The Journal of Neuroscience.

[10]  W. Saltzman Tissue Engineering: Engineering Principles for the Design of Replacement Organs and Tissues , 2004 .

[11]  A. Ramón-Cueto,et al.  Olfactory ensheathing glia transplantation into the injured spinal cord. , 2000, Progress in brain research.

[12]  Jike Lu,et al.  Olfactory Ensheathing Cells: Their Potential Use for Repairing the Injured Spinal Cord , 2002, Spine.

[13]  M. Nieto‐Sampedro,et al.  Glial cells from adult rat olfactory bulb: Immunocytochemical properties of pure cultures of ensheathing cells , 1992, Neuroscience.

[14]  Barber Pc Neurogenesis and regeneration in the primary olfactory pathway of mammals. , 1982 .

[15]  M. Oudega,et al.  Delayed transplantation of olfactory ensheathing glia promotes sparing/regeneration of supraspinal axons in the contused adult rat spinal cord. , 2003, Journal of neurotrauma.

[16]  Bradley R. Ringeisen,et al.  Laser Printing of Single Cells: Statistical Analysis, Cell Viability, and Stress , 2005, Annals of Biomedical Engineering.

[17]  M. Schwab Myelin-associated inhibitors of neurite growth , 1990, Experimental Neurology.

[18]  J. Anders,et al.  New method of purification for establishing primary cultures of ensheathing cells from the adult olfactory bulb , 2001, Glia.

[19]  P. Dijkhuizen,et al.  Ex Vivo Adenoviral Vector-Mediated Neurotrophin Gene Transfer to Olfactory Ensheathing Glia: Effects on Rubrospinal Tract Regeneration, Lesion Size, and Functional Recovery after Implantation in the Injured Rat Spinal Cord , 2003, The Journal of Neuroscience.

[20]  R. Nash Prospects of Stem Cell Transplantation in Autoimmune Diseases , 2004, Journal of Clinical Immunology.

[21]  P M Field,et al.  Repair of adult rat corticospinal tract by transplants of olfactory ensheathing cells. , 1997, Science.

[22]  J A Barron,et al.  Biological Laser Printing: A Novel Technique for Creating Heterogeneous 3-dimensional Cell Patterns , 2004, Biomedical microdevices.

[23]  Bradley R Ringeisen,et al.  Laser printing of pluripotent embryonal carcinoma cells. , 2004, Tissue engineering.

[24]  W. B. Adams,et al.  Why does the central nervous system not regenerate after injury? , 1999, Survey of ophthalmology.

[25]  P. Graziadei,et al.  Continuous Nerve Cell Renewal in the Olfactory System , 1978 .