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. 2004 Jul;15(7):3433–3449. doi: 10.1091/mbc.E03-05-0328

Table 3.

Quantification of neuronal shape parameters in neurons overexpressing wt-LIMK1 and their mutants

Groups No. of primary neurites/cell Total axonal length (μm) No. of collateral branches (axon) No. of growth cone like structures/axon Growth cone area (μm2)
Nontransfected 5.2 ± 0.4 295 ± 22 12 ± 2 1.2 ± 0.2 16 ± 4
wt-LIMK1 5.6 ± 0.2 425 ± 65* 26 ± 4* 5.4 ± 0.6* 46 ± 7*
LIMK1-kd 5.2 ± 0.4 545 ± 44* 45 ± 8* 1.2 ± 0.2 9 ± 2*
Δ-LIM (wt) 5.8 ± 0.4 220 ± 16* 18 ± 6 4.8 ± 0.4* 68 ± 8*
Δ-LIM (kd) 5.2 ± 0.2 636 ± 32* 56 ± 10* 1.6 ± 0.4 8 ± 2
Δ-PDZ (wt) 4.8 ± 0.4 388 ± 14* 22 ± 6* 2.5 ± 0.5 22 ± 8
Δ-PDZ (kd) 5.1 ± 0.7 180 ± 26* 8 ± 4 1.0 ± 0.3 10 ± 2

Each value represents the mean ± SEM. At least 100 cells were analyzed for each experimental condition. Two DIV hippocampal pyramidal cultures were transfected with each of the constructs, fixed 18 h later, and processed for immunofluorescence with a rabbit antibody against HA and a mAb against the class III β-tubulin isotype. Control nontransfected cells had similar neuronal shape parameters to those of cells transfected with GFP alone (6 μg DNA).

*

Values significantly different from those of nontransfected neurons.