The fetal rat binding protein for insulin-like growth factors is expressed in the choroid plexus and cerebrospinal fluid of adult rats

• Published in: Molecular endocrinology (Baltimore, Md.) Vol. 3; no. 10; pp. 1559 - 1568
• Main Authors: TSENG, L. Y.-H, BROWN, A. L, YANG, Y. W.-H, ROMANUS, J. A, ORLOWSKI, C. C, TAYLOR, T, RECHLER, M. M
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Endocrine Society 01.10.1989
• Subjects: Analytical, structural and metabolic biochemistry; Animals; Binding and carrier proteins; Biological and medical sciences; Blotting, Northern; Cerebrospinal Fluid Proteins - genetics; Cerebrospinal Fluid Proteins - metabolism; Choroid Plexus - metabolism; Electrophoresis, Polyacrylamide Gel; Female; Fundamental and applied biological sciences. Psychology; Gene Expression; Histocytochemistry; Male; Nucleic Acid Hybridization; Pregnancy; Protein Binding; Proteins; Rats; RNA, Messenger - genetics; Somatomedins - genetics; Somatomedins - metabolism; Choroid plexus; Molecular hybridization; Rat; Somatomedin C; Rodentia; Central nervous system; Cerebral ventricle; Cerebrospinal fluid; Insulin like growth factor 2; Northern blotting; Proteins; Binding protein; Vertebrata; Mammalia; Messenger RNA; Histochemistry; Growth factor
• DOI: 10.1210/mend-3-10-1559
• ISSN: 0888-8809

The biological effects of the insulin-like growth factors, IGF-I and IGF-II, on their receptors are modulated by IGF-binding proteins. Recently, we isolated a cDNA clone for one member of the family of IGF-binding proteins, BP-3A, a 30 kilodalton (kDa) protein synthesized by the BRL-3A rat liver cell line. BP-3A is related to but distinct from two other cloned IGF-binding proteins, the human amniotic fluid binding protein and the glycosylated binding subunit of the 150 kDa IGF-binding protein complex in serum. It is expressed in multiple nonneural tissues and in serum in the fetal rat and decreases after birth, similar to the developmental pattern of IGF-II expression. IGF-I, IGF-II, and their receptors are expressed in brain. The present study examines the expression of BP-3A in the rat central nervous system. By Northern blot analysis, BP-3A mRNA is present at high levels in brain stem, cerebral cortex, and hypothalamus from 21-day gestation rats and, like IGF-II mRNA, persists in adult rat brain. The site of BP-3A mRNA synthesis was localized by in situ hybridization to coronal sections of adult rat brain using 35S-labeled oligonucleotides, 48 bases in length, complementary and anticomplementary to the coding region of BP-3A. Specific hybridization of the BP-3A probe was observed exclusively to the choroid plexus extending from the level of the medial preoptic nucleus to the arcuate nucleus of the hypothalamus, similar to the previously reported preferential localization of IGF-II mRNA to the choroid plexus. Synthesis of BP-3A mRNA by choroid plexus suggested that BP-3A might be secreted into the cerebrospinal fluid. A 30 kDa IGF-binding protein was demonstrated in rat cerebrospinal fluid that is recognized by antibodies to BP-3A and, like purified BP-3A, has equal affinity for IGF-I and IGF-II. By analogy with other transport proteins synthesized by the choroid plexus, BP-3A may facilitate the secretion of IGF-II to the cerebrospinal fluid and modulate its biological actions at distant sites within the brain.