Transcriptional profiling predicts overwhelming homology of schwann cells, olfactory ensheathing cells, and schwann cell-like glia
Schwann cells (SCs), olfactory ensheathing cells (OECs), and central nervous system Schwann cell‐like glia (SG) represent a group of nerve growth factor receptor p75 (NGFR)‐positive cells, originating from different tissues. Because of their pro‐regenerative capacities, these cells are subjects in e...
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| Published in | Glia Vol. 62; no. 10; pp. 1559 - 1581 |
|---|---|
| Main Authors | , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Blackwell Publishing Ltd
01.10.2014
Wiley Subscription Services, Inc |
| Subjects | |
| Online Access | Get full text |
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| Abstract | Schwann cells (SCs), olfactory ensheathing cells (OECs), and central nervous system Schwann cell‐like glia (SG) represent a group of nerve growth factor receptor p75 (NGFR)‐positive cells, originating from different tissues. Because of their pro‐regenerative capacities, these cells are subjects in experimental transplantation‐based therapies of spinal cord trauma. The objective of this study was to compare the transcriptomes of uninfected and canine distemper virus‐infected OECs, SCs, SG and fibroblasts (FBs) derived from four beagle dogs and cultured under identical conditions in vitro, employing canine genome 2.0 arrays (Affymetrix). Here, we observed a complete lack of transcriptional differerences between OECs and SG, a high similarity of OECs/SG to SCs, and a marked difference of SCs and OECs/SG towards FBs. Differentially expressed genes possibly involved in the maintenance of cell type‐specific identity included an up‐regulation of HOXD8 and HOXC4 in SCs, and an up‐regulation of CNTNAP2 and EFEMP1 in OECs/SG. We identified cell type‐specific biomarkers employing supervised clustering with a K‐nearest‐neighbors algorithm and correlation‐based feature selection. Thereby AQP1 and SCRG1 were predicted to be the most powerful biomarkers distinguishing SCs from OECs/SG. Immunofluorescence confirmed a higher expression of SCRG1 in OECs and SG, and conversely a higher expression of AQP1 in SCs in vitro. Furthermore, canine and murine olfactory nerves showed SCRG1‐positive, AQP1‐negative OECs and/or axons, whereas sciatic nerves displayed multifocal non‐myelinated, AQP1‐positive, SCRG1‐negative cells. Conclusively, OECs/SG are suggested to be a uniform cell type differing only in the tissue of origin and highly related to SCs. GLIA 2014;62:1559–1581
Main Points
Microarray‐based gene expression profiling revealed a complete lack of differentially expressed genes between canine olfactory ensheathing cells and central nervous system Schwann cell‐like glia, and only minor transcriptional differences of both of these compared with peripheral Schwann cells cultured under identical conditions.
Based on the trancriptomic data, AQP1 and SCRG1 were selected as biomarkers to distinguish peripheral Schwann cells from olfactory ensheating cells/central nervous system Schwann cell‐like glia, and this was verified using immunofluorescence in vitro, and immunohistology in canine and mouse olfactory mucosa and sciatic nerve specimens in vivo.
Conclusively, findings suggest that olfactory ensheathing cells and central nervous system Schwann cell‐like glia are a uniform cell type differing only in the tissue of origin and highly related to peripheral Schwann cells. |
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| AbstractList | Schwann cells (SCs), olfactory ensheathing cells (OECs), and central nervous system Schwann cell-like glia (SG) represent a group of nerve growth factor receptor p75 (NGFR)-positive cells, originating from different tissues. Because of their pro-regenerative capacities, these cells are subjects in experimental transplantation-based therapies of spinal cord trauma. The objective of this study was to compare the transcriptomes of uninfected and canine distemper virus-infected OECs, SCs, SG and fibroblasts (FBs) derived from four beagle dogs and cultured under identical conditions in vitro, employing canine genome 2.0 arrays (Affymetrix). Here, we observed a complete lack of transcriptional differerences between OECs and SG, a high similarity of OECs/SG to SCs, and a marked difference of SCs and OECs/SG towards FBs. Differentially expressed genes possibly involved in the maintenance of cell type-specific identity included an up-regulation of HOXD8 and HOXC4 in SCs, and an up-regulation of CNTNAP2 and EFEMP1 in OECs/SG. We identified cell type-specific biomarkers employing supervised clustering with a K-nearest-neighbors algorithm and correlation-based feature selection. Thereby AQP1 and SCRG1 were predicted to be the most powerful biomarkers distinguishing SCs from OECs/SG. Immunofluorescence confirmed a higher expression of SCRG1 in OECs and SG, and conversely a higher expression of AQP1 in SCs in vitro. Furthermore, canine and murine olfactory nerves showed SCRG1-positive, AQP1-negative OECs and/or axons, whereas sciatic nerves displayed multifocal non-myelinated, AQP1-positive, SCRG1-negative cells. Conclusively, OECs/SG are suggested to be a uniform cell type differing only in the tissue of origin and highly related to SCs. GLIA 2014;62:1559-1581 Main Points Microarray-based gene expression profiling revealed a complete lack of differentially expressed genes between canine olfactory ensheathing cells and central nervous system Schwann cell-like glia, and only minor transcriptional differences of both of these compared with peripheral Schwann cells cultured under identical conditions. Based on the trancriptomic data, AQP1 and SCRG1 were selected as biomarkers to distinguish peripheral Schwann cells from olfactory ensheating cells/central nervous system Schwann cell-like glia, and this was verified using immunofluorescence in vitro, and immunohistology in canine and mouse olfactory mucosa and sciatic nerve specimens in vivo. Conclusively, findings suggest that olfactory ensheathing cells and central nervous system Schwann cell-like glia are a uniform cell type differing only in the tissue of origin and highly related to peripheral Schwann cells. [PUBLICATION ABSTRACT] Schwann cells (SCs), olfactory ensheathing cells (OECs), and central nervous system Schwann cell-like glia (SG) represent a group of nerve growth factor receptor p75 (NGFR)-positive cells, originating from different tissues. Because of their pro-regenerative capacities, these cells are subjects in experimental transplantation-based therapies of spinal cord trauma. The objective of this study was to compare the transcriptomes of uninfected and canine distemper virus-infected OECs, SCs, SG and fibroblasts (FBs) derived from four beagle dogs and cultured under identical conditions in vitro, employing canine genome 2.0 arrays (Affymetrix). Here, we observed a complete lack of transcriptional differerences between OECs and SG, a high similarity of OECs/SG to SCs, and a marked difference of SCs and OECs/SG towards FBs. Differentially expressed genes possibly involved in the maintenance of cell type-specific identity included an up-regulation of HOXD8 and HOXC4 in SCs, and an up-regulation of CNTNAP2 and EFEMP1 in OECs/SG. We identified cell type-specific biomarkers employing supervised clustering with a K-nearest-neighbors algorithm and correlation-based feature selection. Thereby AQP1 and SCRG1 were predicted to be the most powerful biomarkers distinguishing SCs from OECs/SG. Immunofluorescence confirmed a higher expression of SCRG1 in OECs and SG, and conversely a higher expression of AQP1 in SCs in vitro. Furthermore, canine and murine olfactory nerves showed SCRG1-positive, AQP1-negative OECs and/or axons, whereas sciatic nerves displayed multifocal non-myelinated, AQP1-positive, SCRG1-negative cells. Conclusively, OECs/SG are suggested to be a uniform cell type differing only in the tissue of origin and highly related to SCs.Schwann cells (SCs), olfactory ensheathing cells (OECs), and central nervous system Schwann cell-like glia (SG) represent a group of nerve growth factor receptor p75 (NGFR)-positive cells, originating from different tissues. Because of their pro-regenerative capacities, these cells are subjects in experimental transplantation-based therapies of spinal cord trauma. The objective of this study was to compare the transcriptomes of uninfected and canine distemper virus-infected OECs, SCs, SG and fibroblasts (FBs) derived from four beagle dogs and cultured under identical conditions in vitro, employing canine genome 2.0 arrays (Affymetrix). Here, we observed a complete lack of transcriptional differerences between OECs and SG, a high similarity of OECs/SG to SCs, and a marked difference of SCs and OECs/SG towards FBs. Differentially expressed genes possibly involved in the maintenance of cell type-specific identity included an up-regulation of HOXD8 and HOXC4 in SCs, and an up-regulation of CNTNAP2 and EFEMP1 in OECs/SG. We identified cell type-specific biomarkers employing supervised clustering with a K-nearest-neighbors algorithm and correlation-based feature selection. Thereby AQP1 and SCRG1 were predicted to be the most powerful biomarkers distinguishing SCs from OECs/SG. Immunofluorescence confirmed a higher expression of SCRG1 in OECs and SG, and conversely a higher expression of AQP1 in SCs in vitro. Furthermore, canine and murine olfactory nerves showed SCRG1-positive, AQP1-negative OECs and/or axons, whereas sciatic nerves displayed multifocal non-myelinated, AQP1-positive, SCRG1-negative cells. Conclusively, OECs/SG are suggested to be a uniform cell type differing only in the tissue of origin and highly related to SCs. Schwann cells (SCs), olfactory ensheathing cells (OECs), and central nervous system Schwann cell-like glia (SG) represent a group of nerve growth factor receptor p75 (NGFR)-positive cells, originating from different tissues. Because of their pro-regenerative capacities, these cells are subjects in experimental transplantation-based therapies of spinal cord trauma. The objective of this study was to compare the transcriptomes of uninfected and canine distemper virus-infected OECs, SCs, SG and fibroblasts (FBs) derived from four beagle dogs and cultured under identical conditions in vitro, employing canine genome 2.0 arrays (Affymetrix). Here, we observed a complete lack of transcriptional differerences between OECs and SG, a high similarity of OECs/SG to SCs, and a marked difference of SCs and OECs/SG towards FBs. Differentially expressed genes possibly involved in the maintenance of cell type-specific identity included an up-regulation of HOXD8 and HOXC4 in SCs, and an up-regulation of CNTNAP2 and EFEMP1 in OECs/SG. We identified cell type-specific biomarkers employing supervised clustering with a K-nearest-neighbors algorithm and correlation-based feature selection. Thereby AQP1 and SCRG1 were predicted to be the most powerful biomarkers distinguishing SCs from OECs/SG. Immunofluorescence confirmed a higher expression of SCRG1 in OECs and SG, and conversely a higher expression of AQP1 in SCs in vitro. Furthermore, canine and murine olfactory nerves showed SCRG1-positive, AQP1-negative OECs and/or axons, whereas sciatic nerves displayed multifocal non-myelinated, AQP1-positive, SCRG1-negative cells. Conclusively, OECs/SG are suggested to be a uniform cell type differing only in the tissue of origin and highly related to SCs. Schwann cells (SCs), olfactory ensheathing cells (OECs), and central nervous system Schwann cell‐like glia (SG) represent a group of nerve growth factor receptor p75 (NGFR)‐positive cells, originating from different tissues. Because of their pro‐regenerative capacities, these cells are subjects in experimental transplantation‐based therapies of spinal cord trauma. The objective of this study was to compare the transcriptomes of uninfected and canine distemper virus‐infected OECs, SCs, SG and fibroblasts (FBs) derived from four beagle dogs and cultured under identical conditions in vitro , employing canine genome 2.0 arrays (Affymetrix). Here, we observed a complete lack of transcriptional differerences between OECs and SG, a high similarity of OECs/SG to SCs, and a marked difference of SCs and OECs/SG towards FBs. Differentially expressed genes possibly involved in the maintenance of cell type‐specific identity included an up‐regulation of HOXD8 and HOXC4 in SCs, and an up‐regulation of CNTNAP2 and EFEMP1 in OECs/SG. We identified cell type‐specific biomarkers employing supervised clustering with a K‐nearest‐neighbors algorithm and correlation‐based feature selection. Thereby AQP1 and SCRG1 were predicted to be the most powerful biomarkers distinguishing SCs from OECs/SG. Immunofluorescence confirmed a higher expression of SCRG1 in OECs and SG, and conversely a higher expression of AQP1 in SCs in vitro . Furthermore, canine and murine olfactory nerves showed SCRG1‐positive, AQP1‐negative OECs and/or axons, whereas sciatic nerves displayed multifocal non‐myelinated, AQP1‐positive, SCRG1‐negative cells. Conclusively, OECs/SG are suggested to be a uniform cell type differing only in the tissue of origin and highly related to SCs. GLIA 2014;62:1559–1581 Microarray‐based gene expression profiling revealed a complete lack of differentially expressed genes between canine olfactory ensheathing cells and central nervous system Schwann cell‐like glia, and only minor transcriptional differences of both of these compared with peripheral Schwann cells cultured under identical conditions. Based on the trancriptomic data, AQP1 and SCRG1 were selected as biomarkers to distinguish peripheral Schwann cells from olfactory ensheating cells/central nervous system Schwann cell‐like glia, and this was verified using immunofluorescence in vitro, and immunohistology in canine and mouse olfactory mucosa and sciatic nerve specimens in vivo. Conclusively, findings suggest that olfactory ensheathing cells and central nervous system Schwann cell‐like glia are a uniform cell type differing only in the tissue of origin and highly related to peripheral Schwann cells. Schwann cells (SCs), olfactory ensheathing cells (OECs), and central nervous system Schwann cell-like glia (SG) represent a group of nerve growth factor receptor p75 (NGFR)-positive cells, originating from different tissues. Because of their pro-regenerative capacities, these cells are subjects in experimental transplantation-based therapies of spinal cord trauma. The objective of this study was to compare the transcriptomes of uninfected and canine distemper virus-infected OECs, SCs, SG and fibroblasts (FBs) derived from four beagle dogs and cultured under identical conditions in vitro, employing canine genome 2.0 arrays (Affymetrix). Here, we observed a complete lack of transcriptional differerences between OECs and SG, a high similarity of OECs/SG to SCs, and a marked difference of SCs and OECs/SG towards FBs. Differentially expressed genes possibly involved in the maintenance of cell type-specific identity included an up-regulation of HOXD8 and HOXC4 in SCs, and an up-regulation of CNTNAP2 and EFEMP1 in OECs/SG. We identified cell type-specific biomarkers employing supervised clustering with a K-nearest-neighbors algorithm and correlation-based feature selection. Thereby AQP1 and SCRG1 were predicted to be the most powerful biomarkers distinguishing SCs from OECs/SG. Immunofluorescence confirmed a higher expression of SCRG1 in OECs and SG, and conversely a higher expression of AQP1 in SCs in vitro. Furthermore, canine and murine olfactory nerves showed SCRG1-positive, AQP1-negative OECs and/or axons, whereas sciatic nerves displayed multifocal non-myelinated, AQP1-positive, SCRG1-negative cells. Conclusively, OECs/SG are suggested to be a uniform cell type differing only in the tissue of origin and highly related to SCs. GLIA 2014; 62:1559-1581 Main Points * Microarray-based gene expression profiling revealed a complete lack of differentially expressed genes between canine olfactory ensheathing cells and central nervous system Schwann cell-like glia, and only minor transcriptional differences of both of these compared with peripheral Schwann cells cultured under identical conditions. * Based on the trancriptomic data, AQP1 and SCRG1 were selected as biomarkers to distinguish peripheral Schwann cells from olfactory ensheating cells/central nervous system Schwann cell-like glia, and this was verified using immunofluorescence in vitro, and immunohistology in canine and mouse olfactory mucosa and sciatic nerve specimens in vivo. * Conclusively, findings suggest that olfactory ensheathing cells and central nervous system Schwann cell-like glia are a uniform cell type differing only in the tissue of origin and highly related to peripheral Schwann cells. Schwann cells (SCs), olfactory ensheathing cells (OECs), and central nervous system Schwann cell‐like glia (SG) represent a group of nerve growth factor receptor p75 (NGFR)‐positive cells, originating from different tissues. Because of their pro‐regenerative capacities, these cells are subjects in experimental transplantation‐based therapies of spinal cord trauma. The objective of this study was to compare the transcriptomes of uninfected and canine distemper virus‐infected OECs, SCs, SG and fibroblasts (FBs) derived from four beagle dogs and cultured under identical conditions in vitro, employing canine genome 2.0 arrays (Affymetrix). Here, we observed a complete lack of transcriptional differerences between OECs and SG, a high similarity of OECs/SG to SCs, and a marked difference of SCs and OECs/SG towards FBs. Differentially expressed genes possibly involved in the maintenance of cell type‐specific identity included an up‐regulation of HOXD8 and HOXC4 in SCs, and an up‐regulation of CNTNAP2 and EFEMP1 in OECs/SG. We identified cell type‐specific biomarkers employing supervised clustering with a K‐nearest‐neighbors algorithm and correlation‐based feature selection. Thereby AQP1 and SCRG1 were predicted to be the most powerful biomarkers distinguishing SCs from OECs/SG. Immunofluorescence confirmed a higher expression of SCRG1 in OECs and SG, and conversely a higher expression of AQP1 in SCs in vitro. Furthermore, canine and murine olfactory nerves showed SCRG1‐positive, AQP1‐negative OECs and/or axons, whereas sciatic nerves displayed multifocal non‐myelinated, AQP1‐positive, SCRG1‐negative cells. Conclusively, OECs/SG are suggested to be a uniform cell type differing only in the tissue of origin and highly related to SCs. GLIA 2014;62:1559–1581 Main Points Microarray‐based gene expression profiling revealed a complete lack of differentially expressed genes between canine olfactory ensheathing cells and central nervous system Schwann cell‐like glia, and only minor transcriptional differences of both of these compared with peripheral Schwann cells cultured under identical conditions. Based on the trancriptomic data, AQP1 and SCRG1 were selected as biomarkers to distinguish peripheral Schwann cells from olfactory ensheating cells/central nervous system Schwann cell‐like glia, and this was verified using immunofluorescence in vitro, and immunohistology in canine and mouse olfactory mucosa and sciatic nerve specimens in vivo. Conclusively, findings suggest that olfactory ensheathing cells and central nervous system Schwann cell‐like glia are a uniform cell type differing only in the tissue of origin and highly related to peripheral Schwann cells. |
| Author | Deschl, Ulrich Baumgärtner, Wolfgang Kalkuhl, Arno Becker, Kathrin Lehmbecker, Annika Kegler, Kristel Ulrich, Reiner Ziege, Susanne Imbschweiler, Ilka Wewetzer, Konstantin |
| Author_xml | – sequence: 1 givenname: Reiner surname: Ulrich fullname: Ulrich, Reiner email: reiner.ulrich@tiho-hannover.de organization: Department of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany – sequence: 2 givenname: Ilka surname: Imbschweiler fullname: Imbschweiler, Ilka organization: Department of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany – sequence: 3 givenname: Arno surname: Kalkuhl fullname: Kalkuhl, Arno organization: Department of Non-Clinical Drug Safety, Boehringer Ingelheim Pharma GmbH&Co KG, Biberach (Riß), Germany – sequence: 4 givenname: Annika surname: Lehmbecker fullname: Lehmbecker, Annika organization: Department of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany – sequence: 5 givenname: Susanne surname: Ziege fullname: Ziege, Susanne organization: Department of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany – sequence: 6 givenname: Kristel surname: Kegler fullname: Kegler, Kristel organization: Department of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany – sequence: 7 givenname: Kathrin surname: Becker fullname: Becker, Kathrin organization: Department of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany – sequence: 8 givenname: Ulrich surname: Deschl fullname: Deschl, Ulrich organization: Department of Non-Clinical Drug Safety, Boehringer Ingelheim Pharma GmbH&Co KG, Biberach (Riß), Germany – sequence: 9 givenname: Konstantin surname: Wewetzer fullname: Wewetzer, Konstantin organization: Department of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany – sequence: 10 givenname: Wolfgang surname: Baumgärtner fullname: Baumgärtner, Wolfgang organization: Department of Pathology, University of Veterinary Medicine Hannover, Hannover, Germany |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24889922$$D View this record in MEDLINE/PubMed |
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| CODEN | GLIAEJ |
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| Snippet | Schwann cells (SCs), olfactory ensheathing cells (OECs), and central nervous system Schwann cell‐like glia (SG) represent a group of nerve growth factor... Schwann cells (SCs), olfactory ensheathing cells (OECs), and central nervous system Schwann cell-like glia (SG) represent a group of nerve growth factor... |
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| SubjectTerms | Animals aquaporin 1 Axons - metabolism Axons - ultrastructure Axons - virology biomarker Biomarkers Biomarkers - metabolism canine distemper virus Cells, Cultured Distemper - metabolism Distemper Virus, Canine Dogs Fibroblasts - metabolism Fibroblasts - ultrastructure Fibroblasts - virology Gene expression Gene Expression Profiling Immunohistochemistry Medical research Mice microarray Microarray Analysis Microscopy, Electron nerve growth factor receptor p75 Nervous system Neuroglia - metabolism Neuroglia - ultrastructure Neuroglia - virology Olfactory Nerve - metabolism Olfactory Nerve - ultrastructure Olfactory Nerve - virology Schwann Cells - metabolism Schwann Cells - ultrastructure Schwann Cells - virology Sciatic Nerve - metabolism Sciatic Nerve - ultrastructure stimulator of chondrogenesis 1 Transcription, Genetic |
| Title | Transcriptional profiling predicts overwhelming homology of schwann cells, olfactory ensheathing cells, and schwann cell-like glia |
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