Literature DB >> 2464147

Connectivity of striatal grafts implanted into the ibotenic acid-lesioned striatum--I. Subcortical afferents.

K Wictorin1, O Isacson, W Fischer, F Nothias, M Peschanski, A Björklund.   

Abstract

Subcortical afferents to transplants of fetal striatal tissue, implanted into the excitotoxically lesioned striatum of adult recipient rats, were studied with retrograde and anterograde axonal tracers and immunohistochemistry. One week after a striatal ibotenic acid lesion, involving most of the head of the caudate-putamen, a suspension of fetal striatal tissue (embryonic day 14-15) was injected into the lesioned area. In one group of rats, the ibotenic acid lesion was preceded (10 days) by large intrastriatal injections of True Blue, with injection sites matching the area to be lesioned. This was done to retrogradely pre-label the host brain afferents to the area of the striatum later to be lesioned and grafted. At 3 or 6 months post-transplantation, small injections (50 nl) of rhodamine-labelled latex beads were made into the striatal grafts. In animals where the injections were confined to the graft, retrogradely labelled host brain neurons were found in the thalamus, the substantia nigra, amygdala and dorsal raphe nucleus. Double-labelling analysis revealed that the vast majority of the rhodamine bead-labelled neurons also contained True Blue, which indicates that the host afferents to the graft, to a large extent, were derived from the neurons which normally project to the area of the caudate-putamen which was lesioned by the ibotenic acid injection. To further substantiate these observations a second group of lesioned and grafted animals received unilateral wheatgerm agglutinin-horseradish peroxidase injections into the ipsilateral host thalamus at 4 months post-transplantation in order to anterogradely label the host thalamostriatal axons. In a third group of animals serotonin immunocytochemistry was performed in order to detect possible afferents from the raphe nuclei. In contrast to the serotonin-containing fibers, which were fairly evenly distributed throughout the graft tissue, the peroxidase-labelled thalamic afferents were most prominent in the peripheral zones of the grafts and they were densely aggregated at the graft-host interface. The combined results provide evidence that the intrastriatal grafts receive afferents from the host substantia nigra, thalamus, amygdala and dorsal raphe nucleus, but with different distributions. The afferents from the substantia nigra, amygdala and raphe nuclei seem to distribute throughout the grafted tissue, although they are most dense in the peripheral parts, whereas the thalamic afferents are largely confined to the peripheral areas of the transplants and to the graft-host interface.

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Year:  1988        PMID: 2464147     DOI: 10.1016/0306-4522(88)90288-6

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  12 in total

1.  Intrastriatal transplantation of cross-species fetal striatal cells reduces abnormal movements in a primate model of Huntington disease.

Authors:  P Hantraye; D Riche; M Maziere; O Isacson
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-01       Impact factor: 11.205

Review 2.  Transplantation into the human brain: present status and future possibilities.

Authors:  O Lindvall
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-06       Impact factor: 10.154

3.  Connectivity of fetal neocortical block transplants in the excitotoxically ablated cortex of adult rats.

Authors:  M K Schulz; T P Hogan; A J Castro
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

4.  Intrastriatal grafts derived from fetal striatal primordia. III. Induction of modular patterns of fos-like immunoreactivity by cocaine.

Authors:  F C Liu; S B Dunnett; H A Robertson; A M Graybiel
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

5.  Embryonic striatal grafts reverse the disinhibitory effects of ibotenic acid lesions of the ventral striatum.

Authors:  P J Reading; S B Dunnett
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

6.  Astrocytes from cerebral cortex or striatum attract adult host serotoninergic axons into intrastriatal ventral mesencephalic co-grafts.

Authors:  A Petit; P Pierret; A Vallée; G Doucet
Journal:  J Neurosci       Date:  2001-09-15       Impact factor: 6.167

7.  Amygdalar GABAergic-rich neural grafts attenuate anxiety-like behavior in rats.

Authors:  Miles Gregory Cunningham; Caroline Martine Connor; William A Carlezon; Edward Meloni
Journal:  Behav Brain Res       Date:  2009-06-17       Impact factor: 3.332

8.  Release of acetylcholine and its dopaminergic control in slices from striatal grafts in the ibotenic acid-lesioned rat striatum.

Authors:  T Wichmann; K Wictorin; A Björklund; K Starke
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1988-12       Impact factor: 3.000

9.  Striatal implants protect the host striatum against quinolinic acid toxicity.

Authors:  S H Pearlman; M Levivier; T J Collier; J R Sladek; D M Gash
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

10.  Increased proportion of acetylcholinesterase-rich zones and improved morphological integration in host striatum of fetal grafts derived from the lateral but not the medial ganglionic eminence.

Authors:  P Pakzaban; T W Deacon; L H Burns; O Isacson
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

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