TY - JOUR
T1 - Astrocytes in rat fetal cerebral cortical homografts following implantation into adult rat spinal cord
AU - Connor, James R.
AU - Bernstein, Jerald J.
N1 - Funding Information:
The authors are grateful to Dr Lawrence Eng (VA, Palo Alto CA) for generousl~ supplying the GFAP antiserum This work was supported by the Veterans Administration
PY - 1987/4/14
Y1 - 1987/4/14
N2 - The present experiment examines astrocytes in fetal cerebral cortical homografts to adult rat spinal cords. The purpose of this study is to determine if astrocytes are structurally organized within the graft. Also, the presence of astrogliosis may be an indicator of the metabolic status of the graft. Embryonic cerebral cortex was taken at 14 days gestational age and transplanted into adult spinal cord at the level of the sixth thoracic vertebra. The homografts were examined at the light and electron microscopic levels from 7 days postimplantation (PI) to 6 months PI with glial fibrillary acidic protein antiserum which is specific immunohistochemical marker for astrocytes. At 7 days PI, immunoreactive astrocytes were present only at the periphery of the graft and appeared to be associated with blood vessels. By 30 days PI, normal protoplasmic astrocytes were present throughout the graft. No hypertrophied astrocytes are present at 30 days PI, but the numerical density of astrocytes is greater than that of normal cerebral cortical gray matter. Fibrous astrocytes are present in the periphery of the implant and many of these astrocytes extended their processes between the host and the graft. Occasional glial scarring is observed between the gray matter of the host and graft, but generally no glial scar occurred in the interface between the graft and the host gray matter. By 45 days PI, hypertrophies astrocytes can be seen in the graft, but are confined in this age group to perivascular regions. Gliosis progressed within the graft throughout the duration of the study, predominating within the graft by 5 months PI. The results of this study demonstrate that astrocytic processes can be shared by the host and graft and that the appearance of hypertrophied astrocytes possibly indicating a decrease in the functional capacity in the graft does not occur until after 30 days PI.
AB - The present experiment examines astrocytes in fetal cerebral cortical homografts to adult rat spinal cords. The purpose of this study is to determine if astrocytes are structurally organized within the graft. Also, the presence of astrogliosis may be an indicator of the metabolic status of the graft. Embryonic cerebral cortex was taken at 14 days gestational age and transplanted into adult spinal cord at the level of the sixth thoracic vertebra. The homografts were examined at the light and electron microscopic levels from 7 days postimplantation (PI) to 6 months PI with glial fibrillary acidic protein antiserum which is specific immunohistochemical marker for astrocytes. At 7 days PI, immunoreactive astrocytes were present only at the periphery of the graft and appeared to be associated with blood vessels. By 30 days PI, normal protoplasmic astrocytes were present throughout the graft. No hypertrophied astrocytes are present at 30 days PI, but the numerical density of astrocytes is greater than that of normal cerebral cortical gray matter. Fibrous astrocytes are present in the periphery of the implant and many of these astrocytes extended their processes between the host and the graft. Occasional glial scarring is observed between the gray matter of the host and graft, but generally no glial scar occurred in the interface between the graft and the host gray matter. By 45 days PI, hypertrophies astrocytes can be seen in the graft, but are confined in this age group to perivascular regions. Gliosis progressed within the graft throughout the duration of the study, predominating within the graft by 5 months PI. The results of this study demonstrate that astrocytic processes can be shared by the host and graft and that the appearance of hypertrophied astrocytes possibly indicating a decrease in the functional capacity in the graft does not occur until after 30 days PI.
UR - http://www.scopus.com/inward/record.url?scp=0023253658&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0023253658&partnerID=8YFLogxK
U2 - 10.1016/0006-8993(87)90741-4
DO - 10.1016/0006-8993(87)90741-4
M3 - Article
C2 - 3555702
AN - SCOPUS:0023253658
SN - 0006-8993
VL - 409
SP - 62
EP - 70
JO - Brain research
JF - Brain research
IS - 1
ER -