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发育中和成年大鼠脑中组蛋白H1(0)的差异表达及性腺激素调节

Differential expression and gonadal hormone regulation of histone H1(0) in the developing and adult rat brain.

作者信息

García-Segura L M, Luquín S, Martínez P, Casas M T, Suau P

机构信息

Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad Autónoma de Barcelona, Spain.

出版信息

Brain Res Dev Brain Res. 1993 May 21;73(1):63-70. doi: 10.1016/0165-3806(93)90046-d.

Abstract

The cellular distribution of histone H1(0) has been examined immunohistochemically in the rat brain. H1(0) accumulates in neurons and glial cells during postnatal development. In neurons, immunoreactivity increases progressively from about postnatal day 10, and reaches a distribution pattern similar to that of adult rats by postnatal day 20. Immunoreactivity in glial cells shows a prominent increase from postnatal day 20 to adult age. The accumulation of H1(0) during postnatal development appears to be correlated with terminal differentiation and maturation. Although immunoreactive neurons are widely distributed in all areas of the central nervous system, many neurons do not express immunoreactivity. For instance in the cerebellum, Purkinje neurons are negative. In females, the number of immunoreactive neurons in the arcuate area of the hypothalamus increases during postnatal development. In contrast, the percentage of immunoreactive neurons in males is low at all ages studied. The expression of H1(0) in the ventromedial part of the arcuate is reversibly and negatively regulated during the estrous cycle by the level of plasma estradiol. Ovariectomy increases the number of immunoreactive neurons while the restoration of the physiological levels of estradiol results in the opposite effect. Early postnatal androgenization of females suppresses the increment in the number of immunoreactive neurons in both the dorsolateral and the ventromedial parts of the arcuate during postnatal development, thus leading to permanently decreased levels of H1(0) immunoreactivity in postpuberal females.

摘要

已采用免疫组织化学方法研究了组蛋白H1(0)在大鼠脑内的细胞分布情况。在出生后发育过程中,H1(0)在神经元和神经胶质细胞中积累。在神经元中,免疫反应性从出生后第10天左右开始逐渐增加,到出生后第20天达到与成年大鼠相似的分布模式。神经胶质细胞中的免疫反应性在出生后第20天到成年期显著增加。出生后发育过程中H1(0)的积累似乎与终末分化和成熟相关。尽管免疫反应性神经元广泛分布于中枢神经系统的所有区域,但许多神经元并不表达免疫反应性。例如在小脑中,浦肯野神经元呈阴性。在雌性大鼠中,下丘脑弓状区域免疫反应性神经元的数量在出生后发育过程中增加。相比之下,在所有研究年龄阶段,雄性大鼠中免疫反应性神经元的百分比都很低。弓状核腹内侧部分H1(0)的表达在发情周期中受到血浆雌二醇水平的可逆性负调控。卵巢切除增加了免疫反应性神经元的数量,而恢复雌二醇的生理水平则产生相反的效果。雌性大鼠出生后早期雄激素化会抑制出生后发育过程中弓状核背外侧和腹内侧部分免疫反应性神经元数量的增加,从而导致青春期后雌性大鼠H1(0)免疫反应性水平永久性降低。

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