Transplantation of Fetal Kidney Tissue Reduces Cerebral Infarction Induced by Middle Cerebral Artery Ligation
Open Access
- 1 December 1999
- journal article
- research article
- Published by SAGE Publications in Journal of Cerebral Blood Flow & Metabolism
- Vol. 19 (12) , 1329-1335
- https://doi.org/10.1097/00004647-199912000-00006
Abstract
The authors, and others, have recently reported that intracerebral administration of glial cell line-derived neurotrophic factor (GDNF) or osteogenic protein-1 protects against ischemia-induced injury in the cerebral cortex of adult rats. Because these trophic factors are highly expressed in the fetal, but not adult, kidney cortex, the possibility that transplantation of fetal kidney tissue could serve as a cellular reservoir for such molecules and protect against ischemic injury in cerebral cortex was examined. Fetal kidneys obtained from rat embryos at gestational day 16, and adult kidney cortex, were dissected and cut into small pieces. Adult male Sprague-Dawley rats were anesthetized with chloral hydrate and placed in a stereotactic apparatus. Kidney tissues were transplanted into three cortical areas adjacent to the right middle cerebral artery (MCA). Thirty minutes after grafting, the right MCA was transiently ligated for 90 minutes. Twenty-four hours after the onset of reperfusion, animals were evaluated behaviorally. It was found that the stroke animals that received adult kidney transplantation developed motor imbalance. However, animals that received fetal kidney grafts showed significant behavioral improvement. Animals were later sacrificed and brains were removed for triphenyltetrazolium chloride staining, Pax-2 immunostaining, and GDNF mRNA expression. It was noted that transplantation of fetal kidney but not adult kidney tissue greatly reduced the volume of infarction in the cerebral cortex. Fetal kidney grafts showed Pax-2 immunoreactivity and GDNF mRNA in the host cerebral cortex. In contrast, GDNF mRNA expression was not found in the adult kidney grafts. Taken together, our data indicate that fetal kidney transplantation reduces ischemia/reperfusion-induced cortical infarction and behavioral deficits in adult rats, and that such tissue grafts could serve as an unique cellular reservoir for trophic factor application to the brain.Keywords
This publication has 46 references indexed in Scilit:
- Osteogenic Protein-1 Protects Against Cerebral Infarction Induced by MCA Ligation in Adult RatsStroke, 1999
- Reduction of Ischemic Brain Injury by Topical Application of Glial Cell Line–Derived Neurotrophic Factor After Permanent Middle Cerebral Artery Occlusion in RatsStroke, 1998
- Transplantation of Fetal Neocortex Ameliorates Sensorimotor and Locomotor Deficits Following Neonatal Ischemic–Hypoxic Brain Injury in RatsExperimental Neurology, 1997
- NMDA induces NO release from primary cell cultures of human fetal cerebral cortexNeuroscience Letters, 1997
- Cellular expression of GDNF mRNA suggests multiple functions inside and outside the nervous systemCell and tissue research, 1996
- TGF-β1 Protects Hippocampal Neurons Against Degeneration Caused by Transient Global IschemiaStroke, 1996
- Ketamine Antagonizes Nitric Oxide Release From Cerebral Cortex After Middle Cerebral Artery Ligation in RatsStroke, 1996
- Glial cell line-derived neurotrophic factor reverses toxin-induced injury to midbrain dopaminergic neurons in vivoNeuroscience Letters, 1994
- A model of focal ischemic stroke in the rat: reproducible extensive cortical infarction.Stroke, 1986
- Rat middle cerebral artery occlusion: evaluation of the model and development of a neurologic examination.Stroke, 1986