Gjerstad M Dreetz, Tandrup T, Koltzenburg M, Jakobsen J
Department of Neurology, Aarhus University Hospital, Denmark.
J Anat. 2002 Jan;200(Pt 1):81-7. doi: 10.1046/j.0021-8782.2001.00003.x.
The significance of the p75 low-affinity neurotrophin receptor, for the maintenance and survival of DRG cells, was studied in p75-deficient mice. Perikarya of the L5 DRG of 12-week-old p75 receptor-deficient mice and healthy Balb C mice were compared using stereological techniques. Following systematic sampling, the optical fractionator and the planar vertical rotator were used to estimate the number and mean volume of the cell bodies of the two neuronal subpopulations. The loss of B-cells was 57% (P < 0.00001), numbers being 7300 (CV = 0.12) in controls and 3100 in p75 receptor-deficient mice (CV = 0.18). Also, A-cells showed a significant loss of 39% (P < 0.0001), numbers being 2600 (CV = 0.12) in control mice and 1500 (CV = 0.16) in p75 receptor-deficient mice. The volume of A-cells was reduced by 30% (P<0.01), from 24.700 microm3 (CV=0.17) perikarya in p75 knock-out mice to 15.100 microm3 (CV=0.17) in controls. B-cell volume did not change significantly. It is concluded that the p75 receptor plays a major role in the survival of DRG cells. The predominant loss of small B-cells indicates that the effect of neurotrophins is dependent upon the presence of the p75 low-affinity receptor.
在p75基因缺陷小鼠中研究了p75低亲和力神经营养因子受体对背根神经节(DRG)细胞维持和存活的意义。使用体视学技术比较了12周龄p75受体缺陷小鼠和健康Balb C小鼠L5 DRG的神经元胞体。经过系统抽样后,使用光学分割器和平面垂直旋转器来估计两个神经元亚群细胞体的数量和平均体积。B细胞损失了57%(P < 0.00001),对照组数量为7300(CV = 0.12),p75受体缺陷小鼠为3100(CV = 0.18)。此外,A细胞显著损失了39%(P < 0.0001),对照小鼠数量为2600(CV = 0.12),p75受体缺陷小鼠为1500(CV = 0.16)。A细胞的体积减少了30%(P<0.01),从p75基因敲除小鼠中每个神经元胞体24700立方微米(CV=0.17)降至对照组的15100立方微米(CV=0.17)。B细胞体积没有显著变化。得出的结论是,p75受体在DRG细胞的存活中起主要作用。小B细胞的大量损失表明神经营养因子的作用依赖于p75低亲和力受体的存在。