18 research outputs found
NG2 and phosphacan are present in the astroglial scar after human traumatic spinal cord injury
BACKGROUND: A major class of axon growth-repulsive molecules associated with CNS scar tissue is the family of chondroitin sulphate proteoglycans (CSPGs). Experimental spinal cord injury (SCI) has demonstrated rapid re-expression of CSPGs at and around the lesion site. The pharmacological digestion of CSPGs in such lesion models results in substantially enhanced axonal regeneration and a significant functional recovery. The potential therapeutic relevance of interfering with CSPG expression or function following experimental injuries seems clear, however, the spatio-temporal pattern of expression of individual members of the CSPG family following human spinal cord injury is only poorly defined. In the present correlative investigation, the expression pattern of CSPG family members NG2, neurocan, versican and phosphacan was studied in the human spinal cord. METHODS: An immunohistochemical investigation in post mortem samples of control and lesioned human spinal cords was performed. All patients with traumatic SCI had been clinically diagnosed as having "complete" injuries and presented lesions of the maceration type. RESULTS: In sections from control spinal cord, NG2 immunoreactivity was restricted to stellate-shaped cells corresponding to oligodendrocyte precursor cells. The distribution patterns of phosphacan, neurocan and versican in control human spinal cord parenchyma were similar, with a fine reticular pattern being observed in white matter (but also located in gray matter for phosphacan). Neurocan staining was also associated with blood vessel walls. Furthermore, phosphacan, neurocan and versican were present in the myelin sheaths of ventral and dorsal nerve roots axons. After human SCI, NG2 and phosphacan were both detected in the evolving astroglial scar. Neurocan and versican were detected exclusively in the lesion epicentre, being associated with infiltrating Schwann cells in the myelin sheaths of invading peripheral nerve fibres from lesioned dorsal roots. CONCLUSION: NG2 and phosphacan were both present in the evolving astroglial scar and, therefore, might play an important role in the blockade of successful CNS regeneration. Neurocan and versican, however, were located at the lesion epicentre, associated with Schwann cell myelin on regenerating peripheral nerve fibres, a distribution that was unlikely to contribute to failed CNS axon regeneration. The present data points to the importance of such correlative investigations for demonstrating the clinical relevance of experimental data
A brief history of muscular dystrophy research: A personal perspective
The field of myology has undergone remarkable changes. From the period
of early clinical descriptions and clinical classifications, new
knowledge of these disorders has come from the developments of
histopathology, enzyme histochemistry and later, immunocytochemistry
and electron microscopy. These techniques have enhanced the
understanding of the pathophysiology of myopathies at the cellular
level. The parallel evolution of molecular genetics has taken the
science further not only by way of understanding and accuracy of
diagnosis, but has opened up exciting possibilities of modulation of
these chronic debilitating diseases. This review gives a personal
perspective of the developments in the field of myology
Binary masses of the earth crust and biosphere
ΠΠΊΡΡΠ°Π»ΡΠ½ΠΎΡΡΡ ΡΠ°Π±ΠΎΡΡ ΠΎΠ±ΡΡΠ»ΠΎΠ²Π»Π΅Π½Π° Π½Π΅ΠΎΠ±Ρ
ΠΎΠ΄ΠΈΠΌΠΎΡΡΡΡ ΡΠΎΠ·Π΄Π°Π½ΠΈΡ ΠΈ Π²Π΅ΡΠΈΡΠΈΠΊΠ°ΡΠΈΠΈ ΠΌΠ°ΡΠ΅ΠΌΠ°ΡΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΌΠΎΠ΄Π΅Π»Π΅ΠΉ Π³Π΅ΠΎΠ»ΠΎΠ³ΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΏΡΠΎΡΠ΅ΡΡΠΎΠ². Π¦Π΅Π»Ρ ΡΠ°Π±ΠΎΡΡ: ΠΎΠΏΡΠ΅Π΄Π΅Π»Π΅Π½ΠΈΠ΅ ΠΏΡΠΈΡΠΎΠ΄Π½ΡΡ
ΠΏΡΠΎΡΠ΅ΡΡΠΎΠ² ΠΈ ΠΎΠ±ΡΠ΅ΠΊΡΠΎΠ², ΠΊΠΎΡΠΎΡΡΠΌ ΡΠΎΠΎΡΠ²Π΅ΡΡΡΠ²ΡΡΡ ΠΌΠ°ΡΠ΅ΠΌΠ°ΡΠΈΡΠ΅ΡΠΊΠΈΠ΅ ΠΌΠΎΠ΄Π΅Π»ΠΈ ΡΠ°Π²Π½ΡΡ
Π°ΡΠΎΠΌΠ½ΡΡ
ΠΌΠ°ΡΡ. ΠΠ΅ΡΠΎΠ΄ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΡ: Π»ΠΎΠ³ΠΈΠΊΠΎ-ΠΌΠ°ΡΠ΅ΠΌΠ°ΡΠΈΡΠ΅ΡΠΊΠΈΠΉ Π°Π½Π°Π»ΠΈΠ· ΡΡΠ΅Π΄Π½ΠΈΡ
ΡΠΎΠ΄Π΅ΡΠΆΠ°Π½ΠΈΠΉ Ρ
ΠΈΠΌΠΈΡΠ΅ΡΠΊΠΈΡ
ΡΠ»Π΅ΠΌΠ΅Π½ΡΠΎΠ² Π² Π·Π΅ΠΌΠ½ΠΎΠΉ ΠΊΠΎΡΠ΅ ΠΈ Π³ΠΈΠ΄ΡΠΎΡΡΠ΅ΡΠ΅ ΠΈ ΠΌΠΎΠ»Π΅ΠΊΡΠ»ΡΡΠ½ΡΡ
ΠΌΠ°ΡΡ ΠΏΡΠΎΠ΄ΡΠΊΡΠΎΠ² ΡΠΎΡΠΎΡΠΈΠ½ΡΠ΅Π·Π°. Π Π΅Π·ΡΠ»ΡΡΠ°ΡΡ. Π ΡΠ΅Π·ΡΠ»ΡΡΠ°ΡΠ΅ Π°Π½Π°Π»ΠΈΠ·Π° ΡΡΠ΅Π΄Π½ΠΈΡ
ΡΠΎΠ΄Π΅ΡΠΆΠ°Π½ΠΈΠΉ Ρ
ΠΈΠΌΠΈΡΠ΅ΡΠΊΠΈΡ
ΡΠ»Π΅ΠΌΠ΅Π½ΡΠΎΠ² Π² Π·Π΅ΠΌΠ½ΠΎΠΉ ΠΊΠΎΡΠ΅ ΠΈ Π³ΠΈΠ΄ΡΠΎΡΡΠ΅ΡΠ΅ ΠΎΠ±ΠΎΡΠ½ΠΎΠ²ΡΠ²Π°Π΅ΡΡΡ ΡΡΡΠ΅ΡΡΠ²ΠΎΠ²Π°Π½ΠΈΠ΅ Π±ΠΈΠ½Π°ΡΠ½ΡΡ
ΠΌΠ°ΡΡ Β«Π³Π°Π·Ρ - Ρ
ΠΈΠΌΠΈΡΠ΅ΡΠΊΠΈΠ΅ ΡΠ»Π΅ΠΌΠ΅Π½ΡΡΒ». Π’Π°ΠΊΠΈΠ΅ ΠΌΠ°ΡΡΡ ΠΏΡΠ΅Π΄Π»Π°Π³Π°Π΅ΡΡΡ Π½Π°Π·Π²Π°ΡΡ ΠΌΠ°ΡΡΠ°ΠΌΠΈ Π€Π΅ΡΡΠΌΠ°Π½Π° ΠΈΠ»ΠΈ F-ΠΌΠ°ΡΡΠ°ΠΌΠΈ. F-ΠΌΠ°ΡΡΡ ΠΏΡΠΎΡΠ²Π»Π΅Π½Ρ Π² ΡΠΎΡΡΠ°Π²Π΅ Π·Π΅ΠΌΠ½Π°Ρ -ΠΎΠΊΠ΅Π°Π½ΠΈΡΠ΅ΡΠΊΠ°Ρ ΠΊΠΎΡΠ°, ΠΊΠΎΠ½ΡΠΈΠ½Π΅Π½ΡΠ°Π»ΡΠ½Π°Ρ Π·Π΅ΠΌΠ½Π°Ρ ΠΊΠΎΡΠ° - Π³ΠΈΠ΄ΡΠΎΡΡΠ΅ΡΠ°, ΠΏΠΎΡΠ²Π΅Π½Π½ΡΠΉ ΡΠ»ΠΎΠΉ - Π°ΡΠΌΠΎΡΡΠ΅ΡΠ° ΠΈ Π΄Ρ. F-ΠΌΠ°ΡΡΡ Π·Π΅ΠΌΠ½ΠΎΠΉ ΠΊΠΎΡΡ Π΄ΠΎΠ»ΠΆΠ½Ρ ΠΏΡΠ΅Π΄ΡΡΠ°Π²Π»ΡΡΡ ΡΠΎΠ±ΠΎΠΉ ΠΏΠΎΠ΄Π²ΠΈΠΆΠ½ΡΠ΅ Π΄ΠΈΡΠΏΠ΅ΡΡΠ½ΡΠ΅ ΡΡΠ΅Π΄Ρ, Π² ΠΊΠΎΡΠΎΡΡΡ
ΡΠ°ΡΠΏΡΠ΅Π΄Π΅Π»Π΅Π½Ρ Π΄ΠΈΡΠΏΠ΅ΡΡΠ½ΡΠ΅ ΡΠ°Π·Ρ. Π‘ΠΎΡΡΠΎΡΠ½ΠΈΠ΅ Π²Π΅ΡΠ΅ΡΡΠ²Π° Ρ ΡΠ°ΠΊΠΈΠΌΠΈ Ρ
Π°ΡΠ°ΠΊΡΠ΅ΡΠΈΡΡΠΈΠΊΠ°ΠΌΠΈ ΠΏΡΠ΅Π΄Π»Π°Π³Π°Π΅ΡΡΡ Π½Π°Π·Π²Π°ΡΡ F-ΡΡΠ΅Π΄ΠΎΠΉ. ΠΠ°ΠΊ Π³Π»ΠΎΠ±Π°Π»ΡΠ½ΡΡ Π±ΠΈΠ½Π°ΡΠ½ΡΡ ΠΌΠ°ΡΡΡ ΠΏΡΠ΅Π΄Π»Π°Π³Π°Π΅ΡΡΡ ΡΠ°ΡΡΠΌΠ°ΡΡΠΈΠ²Π°ΡΡ ΠΠΈΡΠΎΠ²ΠΎΠΉ ΠΎΠΊΠ΅Π°Π½ ΠΈ Π²Π΅ΡΡ
Π½ΡΡ ΡΠ°ΡΡΡ Π»ΠΈΡΠΎΡΡΠ΅ΡΡ, ΠΎΡ ΡΡΠ΅Π΄Π½Π΅ΠΉ Π³ΠΈΠΏΡΠΎΠΌΠ΅ΡΡΠΈΡΠ΅ΡΠΊΠΎΠΉ ΠΎΡΠΌΠ΅ΡΠΊΠΈ Π΄Π½Π° ΠΌΠΈΡΠΎΠ²ΠΎΠ³ΠΎ ΠΎΠΊΠ΅Π°Π½Π° ΠΈ Π²ΡΡΠ΅, Π΄ΠΎ Π½Π΅ΠΊΠΎΡΠΎΡΠΎΠΉ Π³Π»ΡΠ±ΠΈΠ½Ρ ΠΎΡ ΠΏΠΎΠ²Π΅ΡΡ
Π½ΠΎΡΡΠΈ. ΠΠΎΠ½ΡΠΈΠ½Π΅Π½ΡΡ ΠΈ ΠΠΈΡΠΎΠ²ΠΎΠΉ ΠΎΠΊΠ΅Π°Π½ Π² ΠΈΠ½ΡΠ΅ΡΠ²Π°Π»Π΅ Π³ΠΈΠΏΡΠΎΠΌΠ΅ΡΡΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΎΡΠΌΠ΅ΡΠΎΠΊ Β«Π΄Π½ΠΎ - ΡΡΠ΅Π· Π²ΠΎΠ΄Ρ ΠΎΠΊΠ΅Π°Π½Π°Β» ΡΠΎΡΡΠ°Π²Π»ΡΡΡ Π±ΠΈΠ½Π°ΡΠ½ΡΡ ΠΌΠ°ΡΡΡ, ΡΠΎΠΎΡΠ²Π΅ΡΡΡΠ²ΡΡΡΡΡ ΠΏΠΎΠ²Π΅ΡΡ
Π½ΠΎΡΡΡ ΡΠ°Π·Π΄Π΅Π»Π° Π½Π° ΠΊΠΎΠ½ΡΠΈΠ½Π΅Π½ΡΠ°Ρ
ΠΌΡ Π΄ΠΎΠ»ΠΆΠ½Ρ ΠΏΡΠΎΠ²Π΅ΡΡΠΈ Π½Π° ΠΎΡΠΌΠ΅ΡΠΊΠ΅ 312 ΠΌ Π½ΠΈΠΆΠ΅ ΡΡΠΎΠ²Π½Ρ ΠΠΈΡΠΎΠ²ΠΎΠ³ΠΎ ΠΎΠΊΠ΅Π°Π½Π°. ΠΡΠ΅Π΄ΠΏΠΎΠ»Π°Π³Π°Π΅ΡΡΡ, ΡΡΠΎ Π½Π° ΠΊΠΎΠ½ΡΠΈΠ½Π΅Π½ΡΠ°Ρ
ΡΡΠ° ΠΊΠΎΠ½ΡΠΈΠ½Π΅Π½ΡΠ°Π»ΡΠ½ΠΎ-ΠΎΠΊΠ΅Π°Π½ΠΈΡΠ΅ΡΠΊΠ°Ρ ΠΏΠΎΠ²Π΅ΡΡ
Π½ΠΎΡΡΡ ΡΠ°Π²Π½ΡΡ
ΠΌΠ°ΡΡ ΡΠ°ΡΠΏΠΎΠ»Π°Π³Π°Π΅ΡΡΡ ΠΏΡΠΈΠ±Π»ΠΈΠ·ΠΈΡΠ΅Π»ΡΠ½ΠΎ Π½Π° Π³Π»ΡΠ±ΠΈΠ½Π΅ 1187 ΠΌ Π΄Π»Ρ ΡΡΠ°ΡΡΠΊΠΎΠ² ΡΠΎ ΡΡΠ΅Π΄Π½Π΅ΠΉ Π³ΠΈΠΏΡΠΎΠΌΠ΅ΡΡΠΈΡΠ΅ΡΠΊΠΎΠΉ ΠΎΡΠΌΠ΅ΡΠΊΠΎΠΉ ΠΏΠΎΠ²Π΅ΡΡ
Π½ΠΎΡΡΠΈ ΠΊΠΎΠ½ΡΠΈΠ½Π΅Π½ΡΠΎΠ² 875 ΠΌ. ΠΡΠΎΠΉ Π³Π»ΡΠ±ΠΈΠ½Π΅ ΡΠΎΠΎΡΠ²Π΅ΡΡΡΠ²ΡΠ΅Ρ Π½ΠΈΠΆΠ½ΡΡ Π³ΡΠ°Π½ΠΈΡΠ° ΡΠΎΡΠΌΠΈΡΠΎΠ²Π°Π½ΠΈΡ ΡΠ°ΠΊ Π½Π°Π·ΡΠ²Π°Π΅ΠΌΡΡ
ΠΏΡΠΈΠΏΠΎΠ²Π΅ΡΡ
Π½ΠΎΡΡΠ½ΡΡ
ΠΌΠ΅ΡΡΠΎΡΠΎΠΆΠ΄Π΅Π½ΠΈΠΉ (Π΄ΠΎ Π³Π»ΡΠ±ΠΈΠ½Ρ 1-1,5 ΠΊΠΌ) ΠΈ ΠΏΡΠΈΠΏΠΎΠ²Π΅ΡΡ
Π½ΠΎΡΡΠ½ΡΡ
ΡΠΎ ΡΡΠ΅Π΄Π½Π΅Π³Π»ΡΠ±ΠΈΠ½Π½ΡΠΌΠΈ (Π³Π»ΡΠ±ΠΈΠ½Π° ΠΎΡ 0,5 Π΄ΠΎ 1-1,5 ΠΊΠΌ) ΠΈΠ½ΡΡΡΠ·ΠΈΠ²Π½ΡΡ
ΠΌΠ°ΡΡΠΈΠ²ΠΎΠ². ΠΠΎΠ΄ΠΎΠ±Π½ΡΠ΅ ΠΌΠ°ΡΡΡ ΠΎΠ±ΡΠ°Π·ΡΡΡΡΡ ΡΠ°ΠΊΠΆΠ΅ Π² ΡΠ΅Π·ΡΠ»ΡΡΠ°ΡΠ΅ ΡΠΎΡΠΎΡΠΈΠ½ΡΠ΅Π·Π°. Π€ΠΎΡΠΌΠΈΡΠΎΠ²Π°Π½ΠΈΠ΅ ΡΠ°ΠΊΠΈΡ
ΠΌΠ°ΡΡ ΠΏΡΠ΅Π΄ΠΏΠΎΠ»Π°Π³Π°Π΅Ρ ΡΡΡΠ΅ΡΡΠ²ΠΎΠ²Π°Π½ΠΈΠ΅ Π΄ΠΈΡΠΏΠ΅ΡΡΠ½ΡΡ
F-ΡΡΠ΅Π΄. Π‘ΡΡΠ΅ΡΡΠ²ΠΎΠ²Π°Π½ΠΈΠ΅ F-ΠΌΠ°ΡΡ, Π²Π΅ΡΠΎΡΡΠ½ΠΎ, ΠΎΠ±ΡΡΠ»ΠΎΠ²Π»Π΅Π½ΠΎ Π½Π΅ΠΈΠ·Π²Π΅ΡΡΠ½ΡΠΌ ΡΠ°Π½Π΅Π΅ ΡΠ²ΠΎΠΉΡΡΠ²ΠΎΠΌ ΠΌΠ°ΡΠ΅ΡΠΈΠΈ ΡΠΎΡΠΌΠΈΡΠΎΠ²Π°ΡΡ ΡΠ²ΡΠ·Π°Π½Π½ΡΠ΅ Π΄ΡΡΠ³ Ρ Π΄ΡΡΠ³ΠΎΠΌ ΡΠ°Π²Π½ΡΠ΅ ΠΌΠ°ΡΡΡ Ρ Π³ΡΠ°Π²ΠΈΡΠ°ΡΠΈΠΎΠ½Π½ΠΎΠΉ ΠΈ ΠΈΠ½Π΅ΡΡΠΈΠΎΠ½Π½ΠΎΠΉ ΡΠΎΡΡΠ°Π²Π»ΡΡΡΠΈΠΌΠΈ. ΠΡΡΠ²Π»Π΅Π½ΠΈΠ΅ F-ΠΌΠ°ΡΡ ΡΡΠ°Π»ΠΎ Π²ΠΎΠ·ΠΌΠΎΠΆΠ½ΡΠΌ ΠΏΠΎΡΠ»Π΅ ΡΠΎΠ·Π΄Π°Π½ΠΈΡ ΠΌΠ°ΡΠ΅ΠΌΠ°ΡΠΈΡΠ΅ΡΠΊΠΈΡ
ΠΌΠΎΠ΄Π΅Π»Π΅ΠΉ ΡΠ°Π²Π½ΡΡ
Π°ΡΠΎΠΌΠ½ΡΡ
ΠΌΠ°ΡΡ. ΠΠ·ΡΡΠ΅Π½ΠΈΠ΅ F-ΡΠΈΡΡΠ΅ΠΌ ΠΏΡΠ΅Π΄Π»Π°Π³Π°Π΅ΡΡΡ ΠΏΡΠΎΠ²ΠΎΠ΄ΠΈΡΡ Ρ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΠ΅ΠΌ ΠΏΡΠΎΠ³ΡΠ°ΠΌΠΌΡ Agemarker, ΠΊΠΎΡΠΎΡΠ°Ρ ΠΎΡΠ½ΠΎΠ²Π°Π½Π° Π½Π° Π°Π»Π³ΠΎΡΠΈΡΠΌΠ°Ρ
ΠΌΠΎΠ΄Π΅Π»Π΅ΠΉ ΡΠ°Π²Π½ΡΡ
Π°ΡΠΎΠΌΠ½ΡΡ
ΠΌΠ°ΡΡ ΠΈ ΠΈΠΌΠ΅Π΅Ρ ΠΎΡΠΊΡΡΡΡΠΉ ΠΈΡΡ
ΠΎΠ΄Π½ΡΠΉ ΠΊΠΎΠ΄.The relevance of the work is caused by the need to develop and verify mathematical models of geological processes. The main aim of the study is to define natural processes and objects that correspond to mathematical models of equal atomic masses. The methods used in the study is logico-mathematical analysis of average contents of chemical elements in the earth's crust and hydrosphere and molecular masses of photosynthetic products. The results. The analysis of average contents of chemical elements in the earth's crust and hydrosphere substantiates the existence of binary masses Β«gases - chemical elementsΒ». Such masses are proposed to be called Fersman's, or F-masses. F-masses occur in the composition of continental-oceanic crust, continental crust - hydrosphere, soil layer - atmosphere, etc. as mobile dispersed medias with distributed dispersed phases. The state of matter possessing such characteristics is proposed to be called an F-medium. The World Ocean and the upper part of the lithosphere (from the average level of the ocean floor and up to a certain depth from the surface) is considered to be the global binary mass. Binary mass is formed by continents and the World Ocean in the interval of hypsometric marks Β«the ocean floor - edge of the ocean waterΒ»; we must hold the corresponding interface on the continents at 312 m below the level of the World Ocean. It is assumed that this continental-oceanic surface of equal masses is located on the continents approximately at a depth of 1187 m for areas with average hypsometric elevation of 875 m. This depth corresponds to the lower boundary of the formation of near-surface deposits (to the depth of 1-1,5 km) and near-surface deposits with medium-deep (depths from 0,5 to 1-1,5 km) intrusive massifs. F-masses may also be formed as a result of photosynthesis. The formation of such masses presupposes the existence of dispersed medium. The existence of F-masses is probably caused by the previously unknown property of matter to create mutually connected equal masses with gravity and inertial components. The study of F-systems is proposed to be carried out using the Agemarker open source program. The program is based on algorithms of models of equal atomic masses
Matrix metalloproteinases and their inhibitors in human traumatic spinal cord injury-3
<p><b>Copyright information:</b></p><p>Taken from "Matrix metalloproteinases and their inhibitors in human traumatic spinal cord injury"</p><p>http://www.biomedcentral.com/1471-2377/7/17</p><p>BMC Neurology 2007;7():17-17.</p><p>Published online 26 Jun 2007</p><p>PMCID:PMC1914362.</p><p></p>ctions stained with the MMP-1 antibody. Two days after injury, motoneurons in the perilesional area retained their cytoplasmic MMP-1 immunoreactivity. Four days after SCI, MMP-1 immunohistochemistry at the site of injury displayed round to oval cells (arrowheads). By 8 days, the lesion site was filled with a high number of MMP-1 immunoreactive cells. Again, more round to oval shaped cells can be seen. At 11 days after SCI, the amount of MMP-1 stained cells was dramatically decreased and only single round cells were detectable. 4 months after injury, large MMP-1 positive cells could be seen around the site of injury with the morphology of activated astrocytes. 8 months after SCI, identifiable neurons around the lesion site demonstrated a staining pattern similar to that of control cases
Matrix metalloproteinases and their inhibitors in human traumatic spinal cord injury-4
<p><b>Copyright information:</b></p><p>Taken from "Matrix metalloproteinases and their inhibitors in human traumatic spinal cord injury"</p><p>http://www.biomedcentral.com/1471-2377/7/17</p><p>BMC Neurology 2007;7():17-17.</p><p>Published online 26 Jun 2007</p><p>PMCID:PMC1914362.</p><p></p>ctions.8 days after injury. Double immunofluorescence for CD68 (red) and MMP-1 (green). Almost all microglia/macrophages were MMP-1 positive at the lesion site. 8 months after injury. Double immunofluorescence for GFAP (green) and MMP-1 (red). Large, activated, strongly GFAP-positive astrocytes expressing MMP-1 were observed in the glial scar tissue. 11 days after trauma, MMP-2 immunoreactivity (green) was expressed by CD68 positive microglia/macrophages (red) at the lesion site. 2 days after injury, CD68 positive microglia/macrophages (red) were MMP-9 immunoreactive (green) at the lesion epicentre. 24 days after trauma, dense packing of large, CD68 positive macrophages (red) which also stained for MMP-9 (green) was visible at the lesion epicentre. In the same case, double immunofluorescence with CD68 (red) and MMP-12 (green) showed a nearly identical distribution. Eight months after injury, activated GFAP-positive astrocytes (green) displayed TIMP-3 immunoreactivity (red) in the perilesional scar
Matrix metalloproteinases and their inhibitors in human traumatic spinal cord injury-6
<p><b>Copyright information:</b></p><p>Taken from "Matrix metalloproteinases and their inhibitors in human traumatic spinal cord injury"</p><p>http://www.biomedcentral.com/1471-2377/7/17</p><p>BMC Neurology 2007;7():17-17.</p><p>Published online 26 Jun 2007</p><p>PMCID:PMC1914362.</p><p></p>ctions. In a section from patients who died 2 days after SCI, immunohistochemistry for TIMP-1 demonstrated occasional cells (arrow) with a round to oval morphology at the lesion site. Immunohistochemistry for TIMP-2 showed an identical staining pattern, with single immunopositive rounded cells (arrow). At 4 days post injury, identifiable motoneurons demonstrated a cytoplasmic TIMP-2 immunoreactivity. 8 days after SCI, only single neurons (arrow) were stained for TIMP-2 and many motoneurons were unstained (arrowheads). 8 days after trauma, immunohistochemistry for TIMP-3 demonstrated cytoplasmic staining in most identifiable motoneurons close to the site of injury. In the same case, single TIMP-3 immunoreactive round cells could be seen (arrow). Four months after SCI, gray matter of the perilesional area showed mostly TIMP-3 immunoreactive motoneurons. Eight months after injury, multiple activated cells (arrows, presumably astrocytes) were immunopositive for TIMP-3 in areas directly surrounding the dense glial scar