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. 1998 Sep 15;95(19):11354–11359. doi: 10.1073/pnas.95.19.11354

Figure 4.

Figure 4

IL3-Tg exhibit a loss of MN and axonal degeneration in the spinal cord. (AD) ChAT immunoreactivity (ChAT antibody, 1:100) of coronal sections from a 10-month-old control (A and C) or transgenic lumbar spinal cord (B and D). C and D are higher magnifications (×20) of selected areas in A and B (×10), respectively. In addition to their shrunken size, there is a reduced number of ChAT-positive MN in IL3-Tg (B and D) compared with controls (A and C). (EK) NF200 immunoreactivity (NF200 antibody 1:200) of coronal sections from an 11-month-old control (E and G) or transgenic (F and HK) lumbar spinal cord. G and H are higher magnification views (×20) of E and F (×10), respectively. IK are ×40 magnifications of various sections of the same transgenic animal. Note the axonal neuronal degeneration in transgenic (H) compared with controls (G), as monitored by the dramatic loss of NF200 staining. The arrows in HK show the accumulation of neurofilaments in the neuronal cell body and proximal axons of some MN in IL3-Tg. Similar accumulations were also observed at earlier stages of the disease (i.e., presenting a milder paralysis of limbs).