Thomas T, Schreiber G, Jaworowski A
Russell Grimwade School of Biochemistry, University of Melbourne, Parkville, Victoria, Australia.
Dev Biol. 1989 Jul;134(1):38-47. doi: 10.1016/0012-1606(89)90076-6.
The proteins secreted by the choroid plexus throughout rat brain development were analyzed by two-dimensional polyacrylamide gel electrophoresis following biosynthetic labeling of choroid plexus pieces with [14C]leucine in vitro. Approximately 20 major protein species were resolved which, with the exception of transferrin, transthyretin, and alpha 2-macroglobulin, appear to be unrelated to proteins found in high concentrations in plasma. Several patterns of developmental regulation were observed. At least two of the proteins were synthesized and secreted at high levels only by fetal choroid plexus, whereas the secretion of several other proteins including transferrin and proteins comigrating with cystatin C and alpha 2-macroglobulin increased only after birth. The levels of mRNA coding for transferrin, ceruloplasmin, cystatin C, alpha 2-macroglobulin, beta 2-microglobulin, and transthyretin were measured in the brain during development by dot hybridization and northern gel analysis. No mRNA was detected coding for the proteins alpha-fetoprotein, alpha 1-antitrypsin, haptoglobin, and thiostatin in the brain at any stage. For those proteins, which are produced in other parts of the brain as well as by the choroid plexus, the changes in their corresponding mRNA levels measured in whole brain paralleled the changes in their secretion by the choroid plexus. The results presented in this paper show that the choroid plexus is active in protein secretion at all stages studied. The changing pattern of protein secretion by the choroid plexus, combined with its early development compared with other tissues in the brain, suggests that it is active in providing the appropriate extracellular environment for the growth and differentiation of the brain.
在体外使用[14C]亮氨酸对大鼠脉络丛碎片进行生物合成标记后,通过二维聚丙烯酰胺凝胶电泳分析了大鼠脑发育过程中脉络丛分泌的蛋白质。大约分辨出20种主要蛋白质,除转铁蛋白、甲状腺素转运蛋白和α2-巨球蛋白外,这些蛋白质似乎与血浆中高浓度存在的蛋白质无关。观察到了几种发育调控模式。至少有两种蛋白质仅由胎儿脉络丛高水平合成和分泌,而包括转铁蛋白以及与胱抑素C和α2-巨球蛋白共迁移的蛋白质在内的其他几种蛋白质的分泌仅在出生后增加。在发育过程中,通过点杂交和Northern凝胶分析测量了脑中编码转铁蛋白、铜蓝蛋白、胱抑素C、α2-巨球蛋白、β2-微球蛋白和甲状腺素转运蛋白的mRNA水平。在任何阶段的脑中均未检测到编码甲胎蛋白、α1-抗胰蛋白酶、触珠蛋白和硫抑素的mRNA。对于那些在脑的其他部位以及脉络丛中产生的蛋白质,在全脑中测量的其相应mRNA水平的变化与脉络丛中其分泌的变化平行。本文给出的结果表明,在所研究的所有阶段,脉络丛在蛋白质分泌方面都很活跃。脉络丛蛋白质分泌模式的变化,连同其与脑中其他组织相比的早期发育,表明它在为脑的生长和分化提供合适的细胞外环境方面发挥着作用。