Imaging the neonatal motor units at high resolution showed that at birth, each axonal contact to a muscle fiber emanated from a single

branch of a motor axon that could be traced to a proximal bifurcation in the axonal arbor (Figures 1A–1D), as is the case in more mature neuromuscular junctions (Figure 1I). However, in many Screening Library in vitro other ways, the axonal innervation of muscles fibers was different. First, the caliber of axons was significantly smaller when compared to motor axons in older mice (Figure 1F). On average, in the perinatal period, the main branch of the axons that entered the muscle had a diameter of 1.48 ± 0.03 μm (n = 40 measurements from 10 motor units) compared to 4.08 ± 0.07 μm (n = 48 measurements from 12 motor units) at 2 weeks of age (p ≤ 0.0001, Student’s t test). The terminal branches of perinatal motor axons were even finer, and many were measured to be at the diffraction limit of the imaging objective and thus ≤0.22 μm in diameter (NA = 1.4, Alexa 488 emission at 515 nm). A second difference was that axons from the perinatal period were much more branched when compared to the sparse branching found in animals older than 2 weeks of age (compare Figures 1H to 1I). For the most part, the extra branching in perinatal motor Tariquidar in vivo units did not generate blind ends. Rather, as was the case in older animals, >99% of nerve terminal branches terminated on AChR-rich postsynaptic sites. For example, whereas in the cleidomastoid each motor axon

in 2-week-old mice innervated, on average, 18.8 ± 3.0 (n = 5) muscle fibers, each neonatal axon had terminal contacts with the receptor-rich regions on 221 ± 6.1 (n = 5) different muscle fibers, a highly significant 11.8-fold ± 2.2-fold change in size (compare Figures 1E and to 1G, light gray ovals represent the AChR sites, yellow plaques represent AChR sites innervated by the labeled Ergoloid motor unit; p < 0.001, Student's t test). A similar order of magnitude difference in motor unit size relative to motor units in adults was also present in the two other

ventral neck muscles studied (sternomastoid and clavotrapezius) (Table 1). However, in contrast to the change in the size of motor units, the total number of neuromuscular junction sites containing AChRs (labeled with fluorescently tagged alpha bungarotoxin) remained stable from E18 onward (also see below). In the cleidomastoid, for example, there were 410 ± 23 (n = 5) neuromuscular junctions at birth (one per muscle fiber), as compared to 413 ± 13 (n = 5) 2 weeks later (not significantly different [p = 0.898]; Student’s t test). Thus, the greater number of synaptic branches in the perinatal period must be distributed over the same limited number of neuromuscular junctions, demonstrating that each motor axon innervates a 10-fold greater proportion of muscle fibers at birth than 2 weeks later. A third difference between perinatal and older axons was the size and postsynaptic coverage of individual synaptic terminals.