Proteomic Analysis of Cerebrospinal Fluid in Canine Cervical Spondylomyelopathy. Issue 9 (1st May 2015)
- Record Type:
- Journal Article
- Title:
- Proteomic Analysis of Cerebrospinal Fluid in Canine Cervical Spondylomyelopathy. Issue 9 (1st May 2015)
- Main Title:
- Proteomic Analysis of Cerebrospinal Fluid in Canine Cervical Spondylomyelopathy
- Authors:
- Martin-Vaquero, Paula
da Costa, Ronaldo C.
Allen, Matthew J.
Moore, Sarah A.
Keirsey, Jeremy K.
Green, Kari B. - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Study Design.</title> <p>Prospective study.</p> </sec> <sec> <title>Objective.</title> <p>To identify proteins with differential expression in the cerebrospinal fluid (CSF) from 15 clinically normal (control) dogs and 15 dogs with cervical spondylomyelopathy (CSM).</p> </sec> <sec> <title>Summary of Background Data.</title> <p>Canine CSM is a spontaneous, chronic, compressive cervical myelopathy similar to human cervical spondylotic myelopathy. There is a limited knowledge of the molecular mechanisms underlying these conditions. Differentially expressed CSF proteins may contribute with novel information about the disease pathogenesis in both dogs and humans.</p> </sec> <sec> <title>Methods.</title> <p>Protein separation was performed with 2-dimensional electrophoresis. A Student <italic>t</italic> test was used to detect significant differences between groups (<italic>P</italic> &lt; 0.05). Three comparisons were made: (1) control <italic>versus</italic> CSM-affected dogs, (2) control <italic>versus</italic> non–corticosteroid-treated CSM-affected dogs, and (3) non–corticosteroid-treated CSM-affected <italic>versus</italic> corticosteroid-treated CSM-affected dogs. Protein spots exhibiting at least a statistically significant 1.25-fold change between groups were selected for subsequent identification with capillary-liquid chromatography tandem mass spectrometry.</p> </sec> <sec><abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Study Design.</title> <p>Prospective study.</p> </sec> <sec> <title>Objective.</title> <p>To identify proteins with differential expression in the cerebrospinal fluid (CSF) from 15 clinically normal (control) dogs and 15 dogs with cervical spondylomyelopathy (CSM).</p> </sec> <sec> <title>Summary of Background Data.</title> <p>Canine CSM is a spontaneous, chronic, compressive cervical myelopathy similar to human cervical spondylotic myelopathy. There is a limited knowledge of the molecular mechanisms underlying these conditions. Differentially expressed CSF proteins may contribute with novel information about the disease pathogenesis in both dogs and humans.</p> </sec> <sec> <title>Methods.</title> <p>Protein separation was performed with 2-dimensional electrophoresis. A Student <italic>t</italic> test was used to detect significant differences between groups (<italic>P</italic> &lt; 0.05). Three comparisons were made: (1) control <italic>versus</italic> CSM-affected dogs, (2) control <italic>versus</italic> non–corticosteroid-treated CSM-affected dogs, and (3) non–corticosteroid-treated CSM-affected <italic>versus</italic> corticosteroid-treated CSM-affected dogs. Protein spots exhibiting at least a statistically significant 1.25-fold change between groups were selected for subsequent identification with capillary-liquid chromatography tandem mass spectrometry.</p> </sec> <sec> <title>Results.</title> <p>A total of 96 spots had a significant average change of at least 1.25-fold in 1 of the 3 comparisons. Compared with the CSF of control dogs, CSM-affected dogs demonstrated increased CSF expression of 8 proteins including vitamin D-binding protein, gelsolin, creatine kinase B-type, angiotensinogen, α-2-HS-glycoprotein, SPARC (secreted protein, acidic, rich in cysteine), calsyntenin-1, and complement C3, and decreased expression of pigment epithelium-derived factor, prostaglandin-H2 D-isomerase, apolipoprotein E, and clusterin. In the CSF of CSM-affected dogs, corticosteroid treatment increased the expression of haptoglobin, transthyretin isoform 2, cystatin C-like, apolipoprotein E, and clusterin, and decreased the expression of angiotensinogen, α-2-HS-glycoprotein, and gelsolin.</p> </sec> <sec> <title>Conclusion.</title> <p>Many of the differentially expressed proteins are associated with damaged neural tissue, bone turnover, and/or compromised blood-spinal cord barrier. The knowledge of the protein changes that occur in CSM and upon corticosteroid treatment of CSM-affected patients will aid in further understanding the pathomechanisms underlying this disease.</p> <p> <bold>Level of Evidence:</bold> N/A</p> </sec> </abstract> … (more)
- Is Part Of:
- Spine. Volume 40:Issue 9(2015)
- Journal:
- Spine
- Issue:
- Volume 40:Issue 9(2015)
- Issue Display:
- Volume 40, Issue 9 (2015)
- Year:
- 2015
- Volume:
- 40
- Issue:
- 9
- Issue Sort Value:
- 2015-0040-0009-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-05-01
- Subjects:
- Spine -- Abnormalities -- Periodicals
Spine -- Diseases -- Periodicals
Spine -- Surgery -- Periodicals
616.73005 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00007632-000000000-00000 ↗
http://journals.lww.com/spinejournal/pages/default.aspx ↗
http://www.spinejournal.com/ ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/BRS.0000000000000831 ↗
- Languages:
- English
- ISSNs:
- 0362-2436
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8413.903000
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British Library HMNTS - ELD Digital store - Ingest File:
- 4112.xml