Intrastriatal grafts of rat colonic smooth muscle lacking myenteric ganglia stimulate axonal sprouting and regeneration

• Published in: American journal of anatomy 1998-01, Vol.192 (1), p.25-35
• Main Authors: TEW, ELIZABETH M. M., ANDERSON, PATRICK N., SAFFREY, M. JILL, BURNSTOCK, GEOFFREY
• Format: Article
• Language: English
• Subjects: Animals; Axons - physiology; Axons - ultrastructure; CNS regeneration; Colon - transplantation; Colon - ultrastructure; corpus striatum; Corpus Striatum - physiology; Corpus Striatum - ultrastructure; enteric nervous system; Freezing; Gastrointestinal tract; Male; Microscopy, Electron; Muscle, Smooth - transplantation; Muscle, Smooth - ultrastructure; Myenteric Plexus; Nerve Regeneration; Rats; Rats, Inbred F344; Time Factors; transplantation
• ISSN: 0002-9106; 0021-8782; 1553-0795; 1469-7580
• DOI: 10.1046/j.1469-7580.1998.19210025.x

Grafts of living or freeze-killed freshly dissected colonic smooth muscle from young inbred Fischer rats were implanted into the corpus striatum of adult Fischer rats. Sections of brain were examined electron microscopically 3 and 6 wk after implantation. At both times, living grafts were vascularised and contained healthy differentiated smooth muscle cells, fibroblasts, interstitial cells of Cajal and some macrophages. Large bundles of small nonmyelinated axons, identified as CNS axonal sprouts, could be observed in the brain at and near the interface between the living smooth muscle and the CNS tissue. Bundles of regenerating CNS axons, often associated with astrocyte processes, had grown into the grafts. Some axons within the grafts had matured, enlarged and become myelinated by oligodendrocyte processes or Schwann cells. In some cases, smooth muscle cells were observed in close and intricate association with axons. In contrast to the living grafts, grafts of freeze-killed smooth muscle, examined 3 and 6 wk after implantation, contained macrophages, fibroblasts, collagen and large amounts of cellular debris, but no living muscle cells, astrocytes or Schwann cells. The striatal neuropil around freeze-killed grafts did not contain large bundles of CNS axonal sprouts and bundles of axons were not observed within the freeze-killed graft. This study demonstrates that cells from the smooth muscle layers of the colon, in the absence of myenteric ganglia, can stimulate a vigorous regenerative response from CNS axons when implanted into the corpus striatum of adult rats.