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. 2001 Dec 15;21(24):9655–9666. doi: 10.1523/JNEUROSCI.21-24-09655.2001

Table 3.

Effects of injected anti-NF-M on mitochondrial staining

n Mitochondrial clusters per neurite Intensity (IU) per mitochondrial cluster Intensity per unit neurite length (IU/μm) Soma intensity (IU/μm2)
Labeled neurons 23 23.9  ± 2.7 698  ± 92 99.4  ± 7.1 575.2  ± 20.4
Unlabeled neurons 30 24.9  ± 2.4 462  ± 36 64.5  ± 4.5 411.9  ± 20.4
Level of significance NS (p > 0.5) p < 0.05 p < 0.0001 p< 0.0001

Embryos were injected with a mixture of rhodamine–dextran and anti-NF-M at the two-cell stage, then cultured and stained at 24 h after plating with 4-Di-2-Asp, to label mitochondria in living cells. Labeled and unlabeled neurons were descended from the injected and uninjected blastomeres, respectively. Data are from neurons with long neurites (>85 μm) from three separate cultures imaged under the same conditions to quantitate the intensity of 4-Di-2-Asp staining.n represents the number of neurites imaged. The intensities were measured as described in Materials and Methods and are given in relative intensity units (IUs) averaged among neurites (mean ± SE). The statistical levels of significance of the differences between labeled and unlabeled cells were determined by two-tailed ttest.