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. Author manuscript; available in PMC: 2017 Sep 14.
Published in final edited form as: J Neuroendocrinol. 2013 Oct;25(10):863–875. doi: 10.1111/jne.12081

Table 3.

Subcellular Morphology of Gonadotrophs in Male 8-Week-Old Normal and Mutant Mice.

Control FSHβKO FSHRKO LuRKO hpg tfm Gonadectomised
Cell area (μm2) 101 ± 4 94 ± 6 115 ± 9 68 ± 3b 55 ± 3a 106 ± 7 108 ± 3
Cytoplasm area (μm2) 78 ± 4 73 ± 5 90 ± 9 48 ± 2b 33 ± 2a 80 ± 5 87 ± 4
Nuclear area (μm2) 21 ± 3 19 ± 3 26 ± 4 21 ± 4 20 ± 1 25 ± 2 20 ± 2
Granule diameter (nm) 181 ± 5 162 ± 8c 185 ± 15 107 ± 5b 194 ± 8 106 ± 4b 188 ± 9
Granule density (/μm2) 0.15 ± 0.01 0.14 ± 0.01 0.14 ± 0.02 0.06 ± 0.01b 0.07 ± 0.005a 0.06 ± 0.01b 0.05 ± 0.01b
Rough ER (units) 2.6 ± 0.2 2.1 ± 0.2 2.3 ± 0.2 3.2 ± 0.2c 1.3 ± 0.3a 3.9 ± 0.1b 3.8 ± 0.3b
% Granules at perimeter 39 ± 4 32 ± 2 29 ± 5 55 ± 4b 39 ± 3 57 ± 4b 60 ± 2b,
a

P < 0.01 versus normal C3H;

b

P<0.01,

c

P < 0.05 versus control.

Values expressed as the mean ± SEM (n = 4 animals). Three groups of controls were independently assessed C57BL6/129 (transgenic mouse background), C3H (hpg background) and LuRH (transgenic heterozygote). No significant differences were found for each of the parameters measured and, for clarity, the control data shown are from the C57BL6/129 mice.