Mobbs C V, Harlan R E, Burrous M R, Pfaff D W
Rockefeller University, New York, New York 10021.
J Neurosci. 1988 Jan;8(1):113-8. doi: 10.1523/JNEUROSCI.08-01-00113.1988.
Estradiol (E2) facilitates the lordosis reflex that occurs in response to flank stimulation in female rats. Lordosis appears to be regulated in part by the synthesis of proteins in the ventral medial hypothalamus (VMH) that are transported to the midbrain central gray (MCG). We developed a strategy involving microinfusion of radioactive amino acids, followed by 2-dimensional gel electrophoresis, to identify proteins that may be regulated by E2 in the VMH and transported to the MCG. A mixture of 35S-methionine and 35S-cysteine (2:1, total 500-1000 microCi), suspended in 1 microliter PBS, was infused bilaterally into the VMH over a period of 2 hr into matched pairs of ovariectomized female rats, one of which was given a Silastic implant containing E2 at the beginning of infusion or 1 week earlier. The rats were sacrificed 12 hr after the end of infusion, and several brain regions were obtained by microdissection. Samples were analyzed by 2-dimensional gel electrophoresis, entailing isoelectric focusing in the first dimension and SDS-PAGE (molecular-weight separation) in the second dimension, followed by fluorography. We could routinely separate at least 250 spots. We consistently found a protein spot with an apparent molecular weight of 70 kDa, pI of about 5.9, which almost always appeared in the VMH and MCG of rats given E2 replacement but very rarely in samples from ovariectomized rats given no E2 replacement. A spot immediately acidic to this protein (70 kDa, pl about 5.8) appeared to vary inversely with this E2-induced protein.(ABSTRACT TRUNCATED AT 250 WORDS)
雌二醇(E2)可促进雌性大鼠对胁腹刺激产生的脊柱前凸反射。脊柱前凸似乎部分受腹内侧下丘脑(VMH)中蛋白质合成的调节,这些蛋白质会被转运至中脑中央灰质(MCG)。我们开发了一种策略,包括微量注入放射性氨基酸,随后进行二维凝胶电泳,以鉴定可能受E2调节并从VMH转运至MCG的蛋白质。将悬浮于1微升磷酸盐缓冲液(PBS)中的35S-甲硫氨酸和35S-半胱氨酸混合物(2:1,总量500 - 1000微居里)在2小时内双侧微量注入配对的去卵巢雌性大鼠的VMH,其中一组在注入开始时或1周前植入含E2的硅橡胶管。注入结束12小时后处死大鼠,通过显微切割获取几个脑区。样品经二维凝胶电泳分析,第一维进行等电聚焦,第二维进行SDS-聚丙烯酰胺凝胶电泳(分子量分离),随后进行荧光自显影。我们通常能分离出至少250个斑点。我们一直发现一个表观分子量为70 kDa、等电点约为5.9的蛋白质斑点,它几乎总是出现在接受E2替代的大鼠的VMH和MCG中,但在未接受E2替代的去卵巢大鼠的样品中很少出现。与该蛋白质紧邻的一个酸性斑点(70 kDa,等电点约为5.8)似乎与这种E2诱导的蛋白质呈反向变化。(摘要截短于250字)