- Research article
- Open Access
- Open Peer Review
Ascending central canal dilation and progressive ependymal disruption in a contusion model of rodent chronic spinal cord injury
© Radojicic et al; licensee BioMed Central Ltd. 2007
- Received: 22 December 2006
- Accepted: 07 September 2007
- Published: 07 September 2007
Chronic spinal cord injury (SCI) can lead to an insidious decline in motor and sensory function in individuals even years after the initial injury and is accompanied by a slow and progressive cytoarchitectural destruction. At present, no pathological mechanisms satisfactorily explain the ongoing degeneration.
Adult female Sprague-Dawley rats were anesthetized laminectomized at T10 and received spinal cord contusion injuries with a force of 250 kilodynes using an Infinite Horizon Impactor. Animals were randomly distributed into 5 groups and killed 1 (n = 4), 28 (n = 4), 120 (n = 4), 450 (n = 5), or 540 (n = 5) days after injury. Morphometric and immunohistochemical studies were then performed on 1 mm block sections, 6 mm cranial and 6 mm caudal to the lesion epicenter. The SPSS 11.5 t test was used to determine differences between quantitative measures.
Here, we document the first report of an ascending central canal dilation and progressive ependymal disruption cranial to the epicenter of injury in a contusion model of chronic SCI, which was characterized by extensive dural fibrosis and intraparenchymal cystic cavitation. Expansion of the central canal lumen beyond a critical diameter corresponded with ependymal cell ciliary loss, an empirically predictable thinning of the ependymal region, and a decrease in cell proliferation in the ependymal region. Large, aneurysmal dilations of the central canal were accompanied by disruptions in the ependymal layer, periependymal edema and gliosis, and destruction of the adjacent neuropil.
Cells of the ependymal region play an important role in CSF homeostasis, cellular signaling and wound repair in the spinal cord. The possible effects of this ascending pathology on ependymal function are discussed. Our studies suggest central canal dilation and ependymal region disruption as steps in the pathogenesis of chronic SCI, identify central canal dilation as a marker of chronic SCI and provide novel targets for therapeutic intervention.
- Spinal Cord Injury
- Ependymal Cell
- Central Canal
- Aneurysmal Dilation
By the end of the next decade, 300,000 people will be living with chronic spinal cord injury in the US alone . Advances in medical and rehabilitative care have improved survival rates for these individuals, but many experience clinical decline even years after the initial injury. Clinical decline is often accompanied by a slow and progressive cavitation of the central spinal cord, known as post-traumatic syringomyelia (for a review, see ). The pathogenesis of this disease remains poorly understood.
Derangements of cerebrospinal fluid (CSF) dynamics following spinal cord injury are thought to play a role in the initiation and propagation of syringomyelic cysts [3–15]. Normally, CSF circulates in the subarachnoid space, traverses the spinal cord several times a day and exhibits a craniocaudal flow pattern influenced by the cardiac cycle . Some spinal fluid, driven by systolic pulsations, is thought to enter the substance of the cord via the Virchow-Robin perivascular spaces and flow toward the central canal [17, 18], an enigmatic structure of the central spinal cord believed to function as a CSF pathway. Indeed, Storer and colleagues have suggested that fluid flow through the central canal may comprise a 'sink' function whereby harmful metabolites are removed from the cord . Others believe the spinal cord itself produces extracellular fluid, whose egress toward the subarachnoid space or central canal depends on the pressure differential between the two compartments .
Following SCI, normal CSF dynamics may be distorted by a number of possible mechanisms, including subarachnoid CSF outflow obstructions [2, 12], changes in compliance of the subarachnoid space , or elevated intraspinal pressures . Altered CSF dynamics are believed to result in localized spinal cord edema, known as the presyrinx state  that subsequently gives rise to intraspinal cavities and cysts.
The propagation of intraspinal cavities requires a driving force sufficient to propel fluid via a one-way valve mechanism into the cysts and cavities, which often contain fluid at a higher pressure than the subarachnoid space . Proposed driving forces include cardiac pulsations along vessels [4, 17], postural changes and valsalva movements , coalescence of microcysts  and elevated intraspinal pressures . We would additionally suggest consideration of the transient hypertensive episodes of autonomic dysreflexia (for a review, see [24, 25]) and the oncotic pressure of central canal fluid as potential driving forces.
The histological features of syringomyelia have been reproduced in experimental models of the disease. Experimental syringomyelia was first induced reliably with intraspinal injections of the irritant kaolin, producing histological results similar to syringomyelia and, in many respects, acute hydrocephalus . Subsequent models utilized intraspinal injections of excitotoxic compounds and produced pathological results via a physiologically relevant mechanism consistent with the neurochemical milieu known to accompany SCI [5, 26, 27]. Both experimental models suffer the limitation of being non-traumatic  and require the administration of exogenous agents . Mathematical models of syrinx formation allow the study of pressure wave propagations in an idealized cerebrospinal fluid system, but suffer the limitation of not taking into account spinal cord parenchymal changes that may influence patterns of dilation [3, 4, 8–10, 13, 29].
Here, we utilized a clinically relevant contusion model of chronic SCI in hopes of elucidating novel features of this insidious disease. Reminiscent of human syringomyelia, chronic spinal cord injured animals developed cysts and glial-lined cavities of the central spinal cord near the epicenter of injury, which was characterized by extensive dural fibrosis. A prominent ascending and progressive dilation of the central canal lumen cranial to the epicenter of injury was evident over time, presumably due to distensile forces within the canal, and was accompanied by changes in the surrounding ependyma and periependymal tissues. By Laplace's law, we reasoned that dilations in the central canal lumen would result in a wall tension being exerted on the ependymal cells lining the canal that would increase with both the radius and pressure within the canal. We therefore focused our study on the histopathological changes in the ependymal region and periependymal tissues that accompanied the progressive dilation of the central canal.
Spinal cord injury
Adult female Sprague-Dawley rats (n = 22) aged 6–8 weeks and weighing 200–220 grams were anesthetized with intraperitoneal injections of Ketamine (80 mg/kg; Phoenix Pharmaceuticals, Inc. St. Joseph, MO) and Xylazine (10 mg/kg; Phoenix Pharmaceuticals, Inc., St. Joseph, MO). The skin overlying the T8-T11 vertebral levels was shaved and disinfected with provodone scrubs. An incision was made over the T8-T11 spinous processes exposing the underlying paravertebral muscles. Blunt dissection was utilized to expose the transverse processes at T9-T11, and a complete laminectomy was performed at T10. The spinous processes of T9 and T11 were clamped and stabilized using a stereotactic device and a contusion injury with a force of 250 kilodynes was induced using an Infinite Horizon Impactor (Precision Systems and Instrumentation LLC, Fairfax, VA). The overlying muscle was then sutured in layers and the skin stapled with stainless steel wound clips. Post-operative care included bolus injections of subcutaneous saline and prophylactic enrofloxacin (2.5 mg/kg/day; Bayer Corporation, Shawnee Mission, KS). Animals received manual bladder expression twice daily and were inspected for signs of infection, dehydration or autophagia, with appropriate veterinary assistance as needed. All surgical interventions and pre- and post-operative care were conducted in accordance with institutional guidelines.
Animals were randomly distributed into 5 groups and killed 1 (n = 4), 28 (n = 4), 120 (n = 4), 450 (n = 5), or 540 (n = 5) days after injury. Animals in the 1, 28, 120 and 450-day groups were terminally anesthetized and killed by intracardiac perfusion with 4% glutaraldehyde (Fisher Scientific International Inc., Pittsburgh, PA) for resin processing. Animals in the 540-day group received intraperitoneal injections of bromodeoxyuridine (BrdU, 100 mg/kg; Sigma-Aldrich, St. Louis, MO) daily over a two week period prior to terminal anesthesia and killing by intracardiac perfusion with 4% paraformaldehyde for immunohistochemical processing; these spinal cords was dissected and cut in the transverse plane into twelve 1 mm blocks, six blocks cranial to and six blocks caudal to the lesion epicenter. Spinal cords from the 1, 28, 120 and 450-day groups were post-fixed in 4% glutaraldehyde for 72 hours, rinsed in 0.1 M phosphate buffer pH 7.4 for 30 minutes, exposed to 1% OsO4 (Electron Microscopy Sciences, Fort Washington, PA), dehydrated in ascending alcohols, soaked in propylene oxide (Electron Microscopy Sciences, Fort Washington, PA), and embedded in Spurr resin (Electron Microscopy Sciences, Fort Washington, PA), as previously described [30, 31]. Transverse semi-thin (1 um) sections were cut from the cranial face of each block, stained with alkaline toluidine blue (Sigma, St. Louis, MO), cover slipped and examined by light microscopy on an Olympus AX-80 microscope using Olympus Microsuite B3SV software (Olympus America Inc., Melville, NY). For electron microscopy, blocks were trimmed and sections were cut at 100 nm, mounted on copper grids, stained with uranyl acetate and lead citrate, and viewed under a Hitachi EM 600 electron microscope at 75 kV (Hitachi High Technologies America Inc., Schaumburg, IL). For the 540-day group, tissue blocks were cut with a cryostat into 20 μm sections and mounted on gelatin-coated slides for BrdU immunohistochemistry and hematoxylin/eosin staining (Sigma-Aldrich, St. Louis, MO).
For BrdU immunostaining, slide mounted sections from the 540 day group were denatured for 30 minutes using 2 N HCL (Fisher Scientific, Hampton, NH) and then incubated for 30 minutes in 0.1 M phosphate buffer pH 7.4 with 2% bovine serum albumin (Sigma-Aldrich, St. Louis, MO). Sections were incubated overnight at 4 degrees Celsius with a mouse monoclonal anti-BrdU immunoglobulin (Zymed Laboratories, San Francisco, CA). Bound antibody was visualized by incubation in goat anti-mouse Alexa Fluor 594 secondary antibody (Invitrogen, Carlsbad, CA) for 1 hour. Finally, slides were coverslipped and viewed using an Olympus AX-80 microscope using Olympus Microsuite B3SV software (Olympus America Inc., Melville, NY). Standard immunohistochemical controls were utilized and untreated sections and no-primary antibody controls were observed for evidence of autofluorescense.
Sections adjacent to those used for BrdU immunostaining were stained with hematoxylin and eosin according to standard protocol . Hematoxylin/eosin stained sections were observed to verify the presence and characteristics of ependymal region nuclei and to rule out misidentification of infiltrating autofluoresecent cells such as macrophages.
Quantitative analysis of the ependymal region
Five transverse sections sampled at successive 1 mm increments cranial and caudal to the lesion epicenter were analyzed from each animal. Sections were excluded from analyses in cases where secondary non-ependymal lined cavities disrupted the integrity of the central canal. Sections were viewed and digitally photographed with an Olympus AX-80 microscope using Olympus Microsuite B3SV software (Olympus America Inc., Melville, NY). Ependymal region area, central canal luminal area, central canal perimeter and ependymal region nuclear count measurements were made using the Olympus Microsuite B3SV software (Olympus America Inc., Melville, NY). Only clearly stained, round to oval nuclei were counted. Average ependymal region thickness was calculated as the average of eight linear measurements, taken at 8 compass points, from the apical-most ependymal cell processes in contact with the central canal lumen to the basal-most ependymal cell process in contact with the basal lamina of the ependymal region. The ependymal region cellular density was determined by dividing the total ependymal region nuclear count by the corresponding central canal luminal perimeter. Cellular coverage of the central canal was determined by multiplying ependymal region cellular density by the diameter of an average ependymal cell. The SPSS 11.5 t test was used to determine differences between quantitative measures.
The development of successful therapeutic interventions for chronic spinal cord injury necessitates a greater understanding of the pathogenesis of the disease, including the delineation of its histopathological stages. Here, we describe and provide a temporal framework for several histopathological stages of SCI disease progression.
Spinal cord injured rats demonstrated an ascending and progressive dilation of the central canal lumen cranial to the lesion epicenter over time, which was associated with progressive degeneration of the ependymal and peri-ependymal regions. The central canal is an enigmatic structure of the central spinal cord, believed to function as a CSF pathway. Central canal dilation has been noted in autopsy studies of syringomyelic patients  and an ultrastructural analysis of post-traumatic syrinxes revealed ependymal remnants lining portions of the cavity . Using serial MR imaging, Takamura and colleagues have documented a case of post-traumatic progressive central canal dilation leading to syrinx formation in a young adult , but until now this feature has not been fully appreciated in an experimental model of the disease. In our studies, mild to moderate dilations of the central canal lumen were not associated with gross degeneration of the ependymal and peri-ependymal regions, whereas large aneurysmal dilations of the central canal lumen were consistently associated with a circumferential degeneration of the ependymal and peri-ependymal regions, indicating that gray matter degeneration in chronic SCI is preceded by changes in the ependymal region and/or intraluminal cerebrospinal fluid (CSF) dynamics. This pathogenic sequence is consistent with that seen in development of chronic hydrocephalus and suggests that distensile forces within fluid compartments resulting from obstruction may be common feature of the two diseases. Furthermore, the central canal dilation we observed was ascending and asymmetric from the point of injury suggesting a pathologic process beyond the mere loss of volume of surrounding tissue. In spinal cord injury, this ascending pathology may represent a tertiary form of injury arising from disturbances in CSF flow near the epicenter of injury arising from dural fibrosis. Moreover, the slow and progressive nature of the phenomenon may result from transient spikes in hydrostatic pressure, leading to a water hammer effect, and/or changes in intraluminal oncotic pressures that would precede ischemic changes in the cord. In humans, the cystic and cavitary lesions of syringomyelia are known to progress over time and thus the transmission of distensile pressures along the central canal may represent a mechanism by which these lesions can spread to adjacent, uninjured spinal cord segments. Our rodent data indicate that the progression occurred cranial to the lesion epicenter, whereas in humans progression occurs both cranial and caudal to the lesion epicenter. This difference may be influenced by the effects of gravity on the upright posture of humans.
Spinal cord injured rats demonstrated progressive ependymal cell ciliary loss cranial to the lesion epicenter, and a loss of ependymal cell cilia with large dilations of the central canal lumen. Cilia are specialized projections of ependymal cells that promote the flow of CSF within the central canal. Ependymal ciliary loss is known to predispose to hydrocephalus and is a feature of the disease . Therefore, this loss of ependymal cell cilia in the spinal cord may result in altered local CSF homeostasis, resulting in an accumulation of toxic metabolites and oncotic pressures, which could result in damage to the ependymal and periependymal regions. Notably, the ependymal cell layer disruption noted in our study is reminiscent of the ependymal denudation that proceeds the development of severe hydrocephalus in the hyh mouse .
At late time points, large aneurysmal dilations of the central canal lumen were accompanied by denudation of the ependymal cell layer. Normally, ependymal cells form a pseudostratified monolayer of epithelium that regulates fluid and electrolyte balance between the CSF and neuropil . Disruption of the ependymal layer could therefore result in the loss of a protective epithelium. This loss of integrity and competence of the canal could result in exposure of the adjacent grey and white matter to hydrostatic and oncotic pressure gradients, leading to a dissection of stagnant CSF from within the canal into the gray and white matter of the cord, leading to structural and conductive deficits. Indeed, fluid from syringomyelia cysts is known to differ from normal CSF , usually having a higher protein content  and prolonged exposure of peri-ependymal tissues to this microenvironment may lead to its degeneration. In our studies, areas of ependymal denudation were consistently opposed to regions of peri-ependymal edema, gliosis, macrophage infiltration and loss of neuropil. Furthermore, local disruption of the blood brain barrier may contribute to the edema  and subsequent ischemic injury, but may also represent a source of inflammatory molecules and plasma proteins that may adversely influence the microenvironment of nearby cells, including cells with stem/progenitor characteristics, thereby influencing their viability and patterns of differentiation.
It is intriguing to note that large, aneurysmal dilations of the central canal lumen were also associated with decreased proliferation of ependymal region cells. Cells of the ependymal region are vestiges of neuroepithelial cells that give rise to neurons and glia during mammalian development  and are known to orchestrate the regenerative response in tailed amphibians . Ependymal region cells have been shown to proliferate [42, 44–46] and migrate [47–49] following spinal cord injury. This finding has led some authors to speculate on their role in endogenous repair in humans . Indeed, the kinetics of ependymal region cell proliferation and differentiation have been correlated with the recovery of lower limb motor function in rats following contusion injuries . Of note, neural stem cells have been isolated from the CNS [47, 51, 52], including regions near the central canal . Unlike the subventricular zone, the prototypical stem cell niche of the CNS (for a review, see ), multipotent cells of the ependymal region appear restricted to glial lineages [46, 47, 49]. Gliogenesis near the central canal includes the generation of ependymal cells , reactive astrocytes [46, 47, 49], oligodendrocyte precursors  and microglia . Glia are supportive cells of the CNS and are critical for maintaining the structural and functional integrity of the spinal cord after injury . Even reactive astrocytes, long thought to be inhibitory to axonal regeneration, appear to play a role in repair of SCI lesions [46, 58, 59]. Therefore, it stands to reason that disruption of the ependymal stromal epithelium, along with periependymal stem/progenitor cells, may represent a heretofore unrecognized pathogenic mechanism in spinal cord injury, which would hinder gliogenesis in the ependymal region and subsequently wound repair in the spinal cord. Indeed, the progressive disruption of this cell layer, through mechanical and cytotoxic means, could represent a disease mechanism that tips the balance between injury and repair in the spinal cord toward further cytoarchitectural destruction of lesions over time. In principle, this conceptualized disease process should be investigated in other multipotent niches as a basis for understanding related degenerative disorders and sequelae.
This study documents an ascending and progressive central canal dilation and ependymal region destruction rostral to the epicenter of injury in a contusion model of SCI, which was characterized by extensive dural fibrosis near the epicenter of injury. We suggest progressive ependymal region disruption as a novel step in the pathogenesis of chronic spinal cord injury, identify central canal dilation as a potential marker of chronic spinal cord injury and document the ependymal region as a therapeutic target, through cellular rescue or replacement. Our findings share many histological features with chronic hydrocephalus  and suggest that early restoration of favorable CSF hydrodynamics in SCI may prevent further degeneration and provide an environment more hospitable for repair.
We thank Kelly Sharp, Charles Mendoza and Julio Espinoza for assistance with animal surgery and care and Valentina Ciobanu for assistance with histology. This study was funded by the Roman Reed Spinal Cord Injury Research Fund of California, Research for Cure and individual donations to the Reeve-Irvine Research Center.
- Houle JD, Tessler A: Repair of chronic spinal cord injury. ExpNeurol. 2003, 182 (2): 247-260.Google Scholar
- Klekamp J: The pathophysiology of syringomyelia – historical overview and current concept. Acta Neurochir(Wien). 2002, 144 (7): 649-664. 10.1007/s00701-002-0944-3.View ArticleGoogle Scholar
- Berkouk K, Carpenter PW, Lucey AD: Pressure wave propagation in fluid-filled co-axial elastic tubes. Part 1: Basic theory. JBiomechEng. 2003, 125 (6): 852-856.Google Scholar
- Bilston LE, Fletcher DF, Brodbelt AR, Stoodley MA: Arterial pulsation-driven cerebrospinal fluid flow in the perivascular space: a computational model. ComputMethods BiomechBiomedEngin. 2003, 6 (4): 235-241.Google Scholar
- Brodbelt AR, Stoodley MA, Watling A, Rogan C, Tu J, Brown CJ, Burke S, Jones NR: The role of excitotoxic injury in post-traumatic syringomyelia. JNeurotrauma. 2003, 20 (9): 883-893. 10.1089/089771503322385818.View ArticleGoogle Scholar
- Brodbelt AR, Stoodley MA, Watling AM, Tu J, Burke S, Jones NR: Altered subarachnoid space compliance and fluid flow in an animal model of posttraumatic syringomyelia. Spine. 2003, 28 (20): E413-E419. 10.1097/01.BRS.0000092346.83686.B9.View ArticlePubMedGoogle Scholar
- Brodbelt AR, Stoodley MA, Watling AM, Tu J, Jones NR: Fluid flow in an animal model of post-traumatic syringomyelia. EurSpine J. 2003, 12: 300-306.Google Scholar
- Carpenter PW, Berkouk K, Lucey AD: Pressure wave propagation in fluid-filled co-axial elastic tubes. Part 2: Mechanisms for the pathogenesis of syringomyelia. JBiomechEng. 2003, 125 (6): 857-863.Google Scholar
- Chang HS, Nakagawa H: Hypothesis on the pathophysiology of syringomyelia based on simulation of cerebrospinal fluid dynamics. JNeurolNeurosurgPsychiatry. 2003, 74 (3): 344-347.Google Scholar
- Chang HS, Nakagawa H: Theoretical analysis of the pathophysiology of syringomyelia associated with adhesive arachnoiditis. JNeurolNeurosurgPsychiatry. 2004, 75 (5): 754-757.Google Scholar
- Cosan TE, Tel E, Durmaz R, Gulec S, Baycu C: Non-hindbrain-related syringomyelia. Obstruction of the subarachnoid space and the central canal in rats. An experimental study. JNeurosurgSci. 2000, 44 (3): 123-127.Google Scholar
- Klekamp J, Volkel K, Bartels CJ, Samii M: Disturbances of cerebrospinal fluid flow attributable to arachnoid scarring cause interstitial edema of the cat spinal cord. Neurosurgery. 2001, 48 (1): 174-185. 10.1097/00006123-200101000-00031.PubMedGoogle Scholar
- Loth F, Yardimci MA, Alperin N: Hydrodynamic modeling of cerebrospinal fluid motion within the spinal cavity. JBiomechEng. 2001, 123 (1): 71-79.Google Scholar
- Milhorat TH, Nobandegani F, Miller JI, Rao C: Noncommunicating syringomyelia following occlusion of central canal in rats. Experimental model and histological findings. JNeurosurg. 1993, 78 (2): 274-279.View ArticleGoogle Scholar
- Stoodley MA, Gutschmidt B, Jones NR: Cerebrospinal fluid flow in an animal model of noncommunicating syringomyelia. Neurosurgery. 1999, 44 (5): 1065-1075. 10.1097/00006123-199905000-00068.View ArticlePubMedGoogle Scholar
- Menick BJ: Phase-contrast magnetic resonance imaging of cerebrospinal fluid flow in the evaluation of patients with Chiari I malformation. Neurosurg Focus. 2001, 11 (1): 1-4.View ArticleGoogle Scholar
- Stoodley MA, Brown SA, Brown CJ, Jones NR: Arterial pulsation-dependent perivascular cerebrospinal fluid flow into the central canal in the sheep spinal cord. JNeurosurg. 1997, 86 (4): 686-693.View ArticleGoogle Scholar
- Stoodley MA, Jones NR, Brown CJ: Evidence for rapid fluid flow from the subarachnoid space into the spinal cord central canal in the rat. Brain Res. 1996, 707 (2): 155-164. 10.1016/0006-8993(95)01228-1.View ArticlePubMedGoogle Scholar
- Storer KP, Toh J, Stoodley MA, Jones NR: The central canal of the human spinal cord: a computerised 3-D study. JAnat. 1998, 192 (Pt 4): 565-572.Google Scholar
- Fischbein NJ, Dillon WP, Cobbs C, Weinstein PR: The "presyrinx" state: a reversible myelopathic condition that may precede syringomyelia. AJNR AmJNeuroradiol. 1999, 20 (1): 7-20.Google Scholar
- Lederhaus SC, Pritz MB, Pribram HF: Septation in syringomyelia and its possible clinical significance. Neurosurgery. 1988, 22 (6 Pt 1): 1064-1067. 10.1097/00006123-198806010-00015.View ArticlePubMedGoogle Scholar
- Gardner WJ, Angel J: The cause of syringomyelia and its surgical treatment. CleveClinQ. 1958, 25 (1): 4-8.Google Scholar
- Leys D, Petit H, Lesoin F, Combelles G, Jomin M: [Late posttraumatic syringomyelic syndromes. Pathogenetic theories apropos of 3 cases]. Acta neurologica Belgica. 1986, 86 (1): 11-19.PubMedGoogle Scholar
- Bravo G, Guizar-Sahagun G, Ibarra A, Centurion D, Villalon CM: Cardiovascular alterations after spinal cord injury: an overview. CurrMedChemCardiovascHematolAgents. 2004, 2 (2): 133-148.Google Scholar
- Krassioukov AV, Weaver LC: Episodic hypertension due to autonomic dysreflexia in acute and chronic spinal cord-injured rats. AmJPhysiol. 1995, 268 (5 Pt 2): H2077-H2083.Google Scholar
- Schwartz ED, Yezierski RP, Pattany PM, Quencer RM, Weaver RG: Diffusion-weighted MR imaging in a rat model of syringomyelia after excitotoxic spinal cord injury. AJNR AmJNeuroradiol. 1999, 20 (8): 1422-1428.Google Scholar
- Yang L, Jones NR, Stoodley MA, Blumbergs PC, Brown CJ: Excitotoxic model of post-traumatic syringomyelia in the rat. Spine. 2001, 26 (17): 1842-1849. 10.1097/00007632-200109010-00004.View ArticlePubMedGoogle Scholar
- Lee GY, Jones NR, Mayrhofer G, Brown C, Cleland L: Origin of macrophages in a kaolin-induced model of rat syringomyelia: a study using radiation bone marrow chimeras. Spine. 2005, 30 (2): 194-200. 10.1097/01.brs.0000150502.10660.e4.View ArticlePubMedGoogle Scholar
- Bhadelia RA, Bogdan AR, Kaplan RF, Wolpert SM: Cerebrospinal fluid pulsation amplitude and its quantitative relationship to cerebral blood flow pulsations: a phase-contrast MR flow imaging study. Neuroradiology. 1997, 39 (4): 258-264. 10.1007/s002340050404.View ArticlePubMedGoogle Scholar
- Keirstead HS, Blakemore WF: Identification of post-mitotic oligodendrocytes incapable of remyelination within the demyelinated adult spinal cord. JNeuropatholExpNeurol. 1997, 56 (11): 1191-1201.Google Scholar
- Totoiu MO, Keirstead HS: Spinal cord injury is accompanied by chronic progressive demyelination. JCompNeurol. 2005Google Scholar
- Gonzalez R, Glaser J, Liu MT, Lane TE, Keirstead HS: Reducing inflammation decreases secondary degeneration and functional deficit after spinal cord injury. Exp Neurol. 2003, 184 (1): 456-463. 10.1016/S0014-4886(03)00257-7.View ArticlePubMedGoogle Scholar
- Milhorat TH, Capocelli AL, Anzil AP, Kotzen RM, Milhorat RH: Pathological basis of spinal cord cavitation in syringomyelia: analysis of 105 autopsy cases. JNeurosurg. 1995, 82 (5): 802-812.View ArticleGoogle Scholar
- Reddy KK, Del Bigio MR, Sutherland GR: Ultrastructure of the human posttraumatic syrinx. JNeurosurg. 1989, 71 (2): 239-243.View ArticleGoogle Scholar
- Takamura Y, Kawasaki T, Takahashi A, Nunomura K, Tiba K, Hasunuma M, Itou T: A craniocervical injury-induced syringomyelia caused by central canal dilation secondary to acquired tonsillar herniation. Case report. JNeurosurgSpine. 2001, 95 (1): 122-127.View ArticleGoogle Scholar
- Afzelius BA: Cilia-related diseases. JPathol. 2004, 204 (4): 470-477. 10.1002/path.1652.View ArticleGoogle Scholar
- Kiefer M, Eymann R, von TS, Muller A, Steudel WI, Booz KH: The ependyma in chronic hydrocephalus. Childs NervSyst. 1998, 14 (6): 263-270. 10.1007/s003810050222.View ArticleGoogle Scholar
- Jimenez AJ, Tome M, Paez P, Wagner C, Rodriguez S, Fernandez-Llebrez P, Rodriguez EM, Perez-Figares JM: A programmed ependymal denudation precedes congenital hydrocephalus in the hyh mutant mouse. JNeuropatholExpNeurol. 2001, 60 (11): 1105-1119.Google Scholar
- Bruni JE: Ependymal development, proliferation, and functions: a review. MicroscResTech. 1998, 41 (1): 2-13.Google Scholar
- Levine DN: The pathogenesis of syringomyelia associated with lesions at the foramen magnum: a critical review of existing theories and proposal of a new hypothesis. JNeurolSci. 2004, 220 (1–2): 3-21.Google Scholar
- Rossier AB, Foo D, Shillito J, Dyro FM: Posttraumatic cervical syringomyelia. Incidence, clinical presentation, electrophysiological studies, syrinx protein and results of conservative and operative treatment. Brain. 1985, 108 (Pt 2): 439-461. 10.1093/brain/108.2.439.View ArticlePubMedGoogle Scholar
- Vaquero J, Ramiro MJ, Oya S, Cabezudo JM: Ependymal reaction after experimental spinal cord injury. Acta Neurochir(Wien). 1981, 55 (3–4): 295-302. 10.1007/BF01808445.View ArticleGoogle Scholar
- Chernoff EA, Stocum DL, Nye HL, Cameron JA: Urodele spinal cord regeneration and related processes. DevDyn. 2003, 226 (2): 295-307.Google Scholar
- Bruni JE, Anderson WA: Ependyma of the rat fourth ventricle and central canal: response to injury. Acta Anat(Basel). 1987, 128 (4): 265-273.View ArticleGoogle Scholar
- Matthews MA, St Onge MF, Faciane CL: An electron microscopic analysis of abnormal ependymal cell proliferation and envelopment of sprouting axons following spinal cord transection in the rat. Acta Neuropathol(Berl). 1979, 45 (1): 27-36. 10.1007/BF00691801.View ArticleGoogle Scholar
- Takahashi M, Arai Y, Kurosawa H, Sueyoshi N, Shirai S: Ependymal cell reactions in spinal cord segments after compression injury in adult rat. JNeuropatholExpNeurol. 2003, 62 (2): 185-194.Google Scholar
- Johansson CB, Momma S, Clarke DL, Risling M, Lendahl U, Frisen J: Identification of a neural stem cell in the adult mammalian central nervous system. Cell. 1999, 96 (1): 25-34. 10.1016/S0092-8674(00)80956-3.View ArticlePubMedGoogle Scholar
- Kojima A, Tator CH: Intrathecal administration of epidermal growth factor and fibroblast growth factor 2 promotes ependymal proliferation and functional recovery after spinal cord injury in adult rats. JNeurotrauma. 2002, 19 (2): 223-238. 10.1089/08977150252806974.View ArticleGoogle Scholar
- Mothe AJ, Tator CH: Proliferation, migration, and differentiation of endogenous ependymal region stem/progenitor cells following minimal spinal cord injury in the adult rat. Neuroscience. 2005, 131 (1): 177-187. 10.1016/j.neuroscience.2004.10.011.View ArticlePubMedGoogle Scholar
- Beattie MS, Bresnahan JC, Komon J, Tovar CA, Van MM, Anderson DK, Faden AI, Hsu CY, Noble LJ, Salzman S, et al: Endogenous repair after spinal cord contusion injuries in the rat. ExpNeurol. 1997, 148 (2): 453-463.Google Scholar
- Weiss S, Dunne C, Hewson J, Wohl C, Wheatley M, Peterson AC, Reynolds BA: Multipotent CNS stem cells are present in the adult mammalian spinal cord and ventricular neuroaxis. JNeurosci. 1996, 16 (23): 7599-7609.Google Scholar
- Yamamoto S, Yamamoto N, Kitamura T, Nakamura K, Nakafuku M: Proliferation of parenchymal neural progenitors in response to injury in the adult rat spinal cord. ExpNeurol. 2001, 172 (1): 115-127.Google Scholar
- Martens DJ, Seaberg RM, van der KD: In vivo infusions of exogenous growth factors into the fourth ventricle of the adult mouse brain increase the proliferation of neural progenitors around the fourth ventricle and the central canal of the spinal cord. EurJNeurosci. 2002, 16 (6): 1045-1057.Google Scholar
- Doetsch F: A niche for adult neural stem cells. CurrOpinGenetDev. 2003, 13 (5): 543-550.Google Scholar
- Miller RH, Ono K: Morphological analysis of the early stages of oligodendrocyte development in the vertebrate central nervous system. MicroscResTech. 1998, 41 (5): 441-453.Google Scholar
- Carbonell WS, Murase SI, Horwitz AF, Mandell JW: Infiltrative microgliosis: activation and long-distance migration of subependymal microglia following periventricular insults. JNeuroinflammation. 2005, 2 (1): 5-10.1186/1742-2094-2-5.View ArticleGoogle Scholar
- Hauwel M, Furon E, Canova C, Griffiths M, Neal J, Gasque P: Innate (inherent) control of brain infection, brain inflammation and brain repair: the role of microglia, astrocytes, "protective" glial stem cells and stromal ependymal cells. Brain ResBrain ResRev. 2005, 48 (2): 220-233.View ArticleGoogle Scholar
- Faulkner JR, Herrmann JE, Woo MJ, Tansey KE, Doan NB, Sofroniew MV: Reactive astrocytes protect tissue and preserve function after spinal cord injury. JNeurosci. 2004, 24 (9): 2143-2155. 10.1523/JNEUROSCI.3547-03.2004.View ArticleGoogle Scholar
- Talbott JF, Loy DN, Liu Y, Qiu MS, Bunge MB, Rao MS, Whittemore SR: Endogenous Nkx2.2+/Olig2+ oligodendrocyte precursor cells fail to remyelinate the demyelinated adult rat spinal cord in the absence of astrocytes. Experimental Neurology. 2005, 192 (1): 11-24. 10.1016/j.expneurol.2004.05.038.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2377/7/30/prepub
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