Maciejewski-Lenoir D, Jirikowski G F, Sanna P P, Bloom F E
Department of Neuropharmacology, Scripps Research Institute, La Jolla, CA 92037.
Proc Natl Acad Sci U S A. 1993 Feb 15;90(4):1435-9. doi: 10.1073/pnas.90.4.1435.
Magnocellular hypothalamic neurons in Brattleboro rats can accumulate, transport, and translate exogenous [Arg8]vasopressin (AVP) mRNA after injection in the hypothalamo-hypophysial tract in amounts sufficient to reverse transiently the animals' characteristic diabetes insipidus. In the present study, different preparations of hypothalamic RNA extracted from normal rats or synthetic AVP RNA were injected into the lateral hypothalamus of Brattleboro rats. Poly(A)- RNA and poly(A)+ RNA from which tails were removed by RNase H digestion were much more effective than poly(A)+ RNA in expressing AVP in the magnocellular hypothalamic neurons and in raising urine osmolarity. Synthetic AVP RNA lacking a poly(A) tail also produced a very potent dose-dependent diabetes insipidus reversal. Our results suggest that a short or absent poly(A) tail may facilitate the accumulation, transport, or expression of exogenous AVP mRNA by magnocellular neurons.
将外源性[精氨酸8]血管加压素(AVP)mRNA注入布氏大鼠的下丘脑 - 垂体束后,下丘脑大细胞神经元能够积累、运输并翻译该mRNA,其数量足以暂时逆转动物典型的尿崩症。在本研究中,将从正常大鼠提取的不同下丘脑RNA制剂或合成的AVP RNA注入布氏大鼠的下丘脑外侧。经核糖核酸酶H消化去除尾端的聚腺苷酸(poly(A))- RNA和聚腺苷酸(poly(A))+ RNA在大细胞下丘脑神经元中表达AVP以及提高尿渗透压方面比聚腺苷酸(poly(A))+ RNA更有效。缺乏聚腺苷酸尾端的合成AVP RNA也产生了非常有效的剂量依赖性尿崩症逆转作用。我们的结果表明,短的或不存在的聚腺苷酸尾端可能有助于大细胞神经元对外源性AVP mRNA的积累、运输或表达。