The left thumbs and great toes of three 8 1/2 month old Rhesus monkeys (Macaca mulatta) were amputated in guillotine fashion one millimeter distal to the base of the nail and allowed to heal by the conservative open wound method. Healing occurred in seven to ten days in these small digits. Each of the thumbs and toes grew back with some blunting and shortening of the digit tips, but were functional. The new structures were cosmetically pleasing as in the human instances. The nails grew essentially to normal size and shape supported by the remaining portions of the distal phalanges. Histological studies showed no evidence of blastema formation such as is observed in the regenerating limb of the Urodele (newt) taken as the comparative representative. The possibility of improving the regrowth is discussed against the background of our knowledge of the importance of nerve during limb regeneration in lower vertebrates.

Stages in the development of sensory ganglia in the regenerating newt tail after amputation are described by taking advantage of the rostrocaudal developmental gradient of the regenerating tail. A series of ganglia, beginning at the tip of the regenerate and progressing rostrally, were examined. Eight-week regenerates were used because they showed the most complete array of stages. The first recognizable ganglia appear as small clusters of cells sitting dorsally on the already established ventral roots. The cluster of ganglionic cells steadily expands with the addition of many new cells. Signs of cell differentiation within the ganglion precede the formation of the dorsal root rudiment, which assumes several different configurations but most commonly enters the cord close to the ventral root. Our material suggests that ganglion precursor cells originate in the ventral region of the developing spinal cord and migrate out of the cord by travelling along the ventral root until, at a suitable distance from the cord, they halt, proliferate, and eventually differentiate. In the regenerate, we saw no evidence of neural crest cells--such as those that give rise to ganglia in the trunk region during development--forming at the dorsal region of the regenerated neural tube. Nor was there any morphological evidence of mesenchymal contribution to the ganglion cell clusters.

The morphology of early interactions between neural tube and myotome in the amphibian embryo and tail regenerate was examined using the electron microscope. Two types of contacts were observed. At the most primitive level where the myotome was yet unsegmented, multiple adhesive-type contacts linked neural tube and myotome. In newly segmented areas early ventral roots were recognizable as small bundles of one to five axons extending the short distance to the myotome. There was only one bundle per segment and in addition to axons, each bundle always contained one or more primitive glial cell processes which accompanied axons as they left the cord. At points of root exit primitive glial processes appeared to funnel axons into the root. The cytoarchitecture of the cord and the new roots suggested that the primitive glia may play a role in pathfinding for motor axons as they leave the cord and extend toward their targets.

The perineural epithelial cells of the peripheral nerve sheath in triturus are elongated flat cells with long and thin cytoplasmic processes. Structural characteristics of the processes include a relative absence of common cytoplasmic organelles of the perinuclear cytoplasm but an abundance of vesicular profiles similar to fully formed pinocytotic vesicles. Unlike pinocytotic vesicles, vesicles of the processes often contain an 8-nm thick filament attached to their cytoplasmic face. Vesicles are also interconnected by similar filaments or by tubules. In addition, almost all vehicles appear to have openings at the cell surface, a feature not seen for pinocytotic vesicles. The concentration of exogenous peroxidase in the vesicles, and the subsequent appearance of peroxidase in the endoneural fluid, myelin sheath and axon, support the notion that the vesicles function in the exchange of substances between extraneural and endoneural fluids.