TY - JOUR
T1 - Organization of visual cortical projections to fetal tectal transplants in rats
T2 - a study using multiple retrograde tracers
AU - Worthington, Delys R.
AU - Harvey, Alan R.
PY - 1990/12/17
Y1 - 1990/12/17
N2 - Retrograde tracing techniques have been used to study the host visual cortical projection to fetal tectal tissue grafted to the midbrain of newborn host rats. To determine whether there is any topographic order in these cortical afferents, different parts of the grafts were injected with 3 different tracers: Fast blue (FB), Diamidino yellow dihydrochloride (DY), and either horseradish peroxidase (HRP) or rhodamine-labelled microspheres (Rh). The comparative visual cortical distribution of cells retrogradely labelled with the different dyes was then examined. Tectal tissue from 15-day-old pigmented rat embryos was injected via a glass micropipette onto the dorsal midbrain of anaesthetised newborn rats of the same strain. In adulthood, host rats were examined for the presence of grafts; 21 grafts were injected with retrograde tracers and the cortices of 12 of these animals were mapped to show the relative location of FB-, DY-, HRP- or Rh-labelled cells. Qualitative inspection of area 17 did not reveal consistent evidence of point-to-point visuotopic mapping in the cortico-transplant projection. However, within area 17 statistical analysis (X2 tests) revealed significant differences in most brains in the relative distribution of FB-,DY -, HRP- or Rh-labelled neurons. Areas 18 and 18a contained greater numbers of retrogradely labelled cells. In these extrastriate regions, statistical analysis also indicate significant differences in the relative distribution of neurons labelled with different tracers. These data thus provide evidence for a non-random pattern of cortical innervation of tectal grafts. Possible reasons for the absence of coherent, topographically organized cortico-transplant maps typical of the normal corticotectal projection are considered.
AB - Retrograde tracing techniques have been used to study the host visual cortical projection to fetal tectal tissue grafted to the midbrain of newborn host rats. To determine whether there is any topographic order in these cortical afferents, different parts of the grafts were injected with 3 different tracers: Fast blue (FB), Diamidino yellow dihydrochloride (DY), and either horseradish peroxidase (HRP) or rhodamine-labelled microspheres (Rh). The comparative visual cortical distribution of cells retrogradely labelled with the different dyes was then examined. Tectal tissue from 15-day-old pigmented rat embryos was injected via a glass micropipette onto the dorsal midbrain of anaesthetised newborn rats of the same strain. In adulthood, host rats were examined for the presence of grafts; 21 grafts were injected with retrograde tracers and the cortices of 12 of these animals were mapped to show the relative location of FB-, DY-, HRP- or Rh-labelled cells. Qualitative inspection of area 17 did not reveal consistent evidence of point-to-point visuotopic mapping in the cortico-transplant projection. However, within area 17 statistical analysis (X2 tests) revealed significant differences in most brains in the relative distribution of FB-,DY -, HRP- or Rh-labelled neurons. Areas 18 and 18a contained greater numbers of retrogradely labelled cells. In these extrastriate regions, statistical analysis also indicate significant differences in the relative distribution of neurons labelled with different tracers. These data thus provide evidence for a non-random pattern of cortical innervation of tectal grafts. Possible reasons for the absence of coherent, topographically organized cortico-transplant maps typical of the normal corticotectal projection are considered.
KW - Corticotectal pathway
KW - Fluorescent dye
KW - Retrograde transport
KW - Tectal transplant
KW - Visualtopography
UR - http://www.scopus.com/inward/record.url?scp=0025612281&partnerID=8YFLogxK
U2 - 10.1016/0006-8993(90)90020-C
DO - 10.1016/0006-8993(90)90020-C
M3 - Article
C2 - 2085743
AN - SCOPUS:0025612281
VL - 536
SP - 153
EP - 162
JO - Brain Research
JF - Brain Research
SN - 0006-8993
IS - 1-2
ER -