Surface specializations of neurites in embryonic mouse spinal cord. 1976

J E Vaughn, and C K Henrikson

Focal surface specializations occur upon axons, axon growth cone filopodia and, somewhat less frequently, upon dendrites as well as dendritic growth cones in embryonic mouse spinal cord. These surface specializations are observed during the early synaptogenic period (embryonic days 12-16) when the axons of the marginal zone are forming synaptic junctions with motor neuron dendrites growing into their domain. At relatively low electron microscopic magnifications, the specializations appear as discrete patches of electron-dense material located just outside the plasma membrane. Higher resolution and an optimum section plane reveal the following ultrastructural characteristics of these specializations. There is a narrow (approximately 5 nm) less dense layer between the outer surface of the plasms membrane and the thicker (approximately 11.5-15 nm) electron-dense, distal layer of the specializations. The dense layer contains spherical profiles (approximately 10-15 nm in diameter) which have relatively clear centers and non-laminar, opaque perimeters. The surface specializations are commonly associated with an accumulation of dense, fibrillar cytoplasmic material that undercoats the cytoplasmic surface of the plasma membrance directly opposite to the external specializations. Furthermore, some of these surface specializations appear to be forming or merging with the cleft material of protosynaptic junctions and primitive puncta adhaerentia-like contacts. We have also examined the pattern of concanavalin A-peroxidase staining on the cell surfaces in embryonic spinal cord. At embryonic day 13, the earliest stage examined in the concanavalin A-peroxidase experiments, there is already an ubiquitous staining around all the cellular processes in the marginal zone as well as around the perikarya and processes of cells located in the intermediate and ventricular zones. No selective enhancement of neurite surfaces occurred which might have correlated with the surface specializations described above. Finally, the possibility is discussed that the neurite surface specializations might play some role in intercellular recognition phenomena leading to the formation of synaptic junctions and puncta adhaerentia.

UI MeSH Term Description Entries
D008358 Mannose A hexose or fermentable monosaccharide and isomer of glucose from manna, the ash Fraxinus ornus and related plants. (From Grant & Hackh's Chemical Dictionary, 5th ed & Random House Unabridged Dictionary, 2d ed) D-Mannose,Mannopyranose,Mannopyranoside,D Mannose
D009474 Neurons The basic cellular units of nervous tissue. Each neuron consists of a body, an axon, and dendrites. Their purpose is to receive, conduct, and transmit impulses in the NERVOUS SYSTEM. Nerve Cells,Cell, Nerve,Cells, Nerve,Nerve Cell,Neuron
D002462 Cell Membrane The lipid- and protein-containing, selectively permeable membrane that surrounds the cytoplasm in prokaryotic and eukaryotic cells. Plasma Membrane,Cytoplasmic Membrane,Cell Membranes,Cytoplasmic Membranes,Membrane, Cell,Membrane, Cytoplasmic,Membrane, Plasma,Membranes, Cell,Membranes, Cytoplasmic,Membranes, Plasma,Plasma Membranes
D003712 Dendrites Extensions of the nerve cell body. They are short and branched and receive stimuli from other NEURONS. Dendrite
D006027 Glycosides Any compound that contains a constituent sugar, in which the hydroxyl group attached to the first carbon is substituted by an alcoholic, phenolic, or other group. They are named specifically for the sugar contained, such as glucoside (glucose), pentoside (pentose), fructoside (fructose), etc. Upon hydrolysis, a sugar and nonsugar component (aglycone) are formed. (From Dorland, 28th ed; From Miall's Dictionary of Chemistry, 5th ed) Glycoside
D000367 Age Factors Age as a constituent element or influence contributing to the production of a result. It may be applicable to the cause or the effect of a circumstance. It is used with human or animal concepts but should be differentiated from AGING, a physiological process, and TIME FACTORS which refers only to the passage of time. Age Reporting,Age Factor,Factor, Age,Factors, Age
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001369 Axons Nerve fibers that are capable of rapidly conducting impulses away from the neuron cell body. Axon
D013116 Spinal Cord A cylindrical column of tissue that lies within the vertebral canal. It is composed of WHITE MATTER and GRAY MATTER. Coccygeal Cord,Conus Medullaris,Conus Terminalis,Lumbar Cord,Medulla Spinalis,Myelon,Sacral Cord,Thoracic Cord,Coccygeal Cords,Conus Medullari,Conus Terminali,Cord, Coccygeal,Cord, Lumbar,Cord, Sacral,Cord, Spinal,Cord, Thoracic,Cords, Coccygeal,Cords, Lumbar,Cords, Sacral,Cords, Spinal,Cords, Thoracic,Lumbar Cords,Medulla Spinali,Medullari, Conus,Medullaris, Conus,Myelons,Sacral Cords,Spinal Cords,Spinali, Medulla,Spinalis, Medulla,Terminali, Conus,Terminalis, Conus,Thoracic Cords
D013569 Synapses Specialized junctions at which a neuron communicates with a target cell. At classical synapses, a neuron's presynaptic terminal releases a chemical transmitter stored in synaptic vesicles which diffuses across a narrow synaptic cleft and activates receptors on the postsynaptic membrane of the target cell. The target may be a dendrite, cell body, or axon of another neuron, or a specialized region of a muscle or secretory cell. Neurons may also communicate via direct electrical coupling with ELECTRICAL SYNAPSES. Several other non-synaptic chemical or electric signal transmitting processes occur via extracellular mediated interactions. Synapse

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