INVESTIGATION INTO THE POTENTIAL PHYSIOLOGICAL SOURCES OF RAT MILK IGF-I AND IGF-BINDING PROTEINS

Citation
Sm. Donovan et al., INVESTIGATION INTO THE POTENTIAL PHYSIOLOGICAL SOURCES OF RAT MILK IGF-I AND IGF-BINDING PROTEINS, Journal of Endocrinology, 145(3), 1995, pp. 569-578
Citations number
36
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
00220795
Volume
145
Issue
3
Year of publication
1995
Pages
569 - 578
Database
ISI
SICI code
0022-0795(1995)145:3<569:IITPPS>2.0.ZU;2-2
Abstract
We have previously reported the presence of IGF-I and IGF-binding prot eins (IGFBP-2, -3 and -4) in rat milk. Herein, the potential sources o f rat milk IGF-I and IGFBPs were investigated. Lactating dam (day 14 p ostpartum) were separated from their pups and injected intraperitoneal ly with 0.45 mu Ci I-125-IGF-I Or I-125-IGFBP-3. After 3 h, serum and milk of rats receiving I-125-IGF-I contained 7642 +/- 3121 and 14 455 +/- 7837 c.p.m./ml respectively. Serum and milk of rats given I-125-IG FBP-3 contained 7232 +/- 1366 and 10 371 +/- 4091 c.p.m./ml respective ly. Sephacryl S-200 gel filtration chromatography demonstrated that th e I-125-IGF-I in both serum and milk was primarily in the 150 kDa IGF- binding complex, whereas the distribution of I-125-IGFBP-3 differed be tween serum and milk. In serum, most of the I-125-IGFBP-3 was in the 1 50 kDa fraction, while most I-125-IGFBP-3 in milk was in the 40 kDa fr action. Northern analysis of liver showed IGFBP-1 and -3 mRNA expressi on, with variable expression of IGFBP-2 and -4 mRNA. In contrast, mamm ary tissue expressed only IGFBP-2 and -4 mRNA, suggesting that these I GFBPs in milk may arise from de novo synthesis within the mammary glan d. The lack of detectable IGFBP-3 mRNA in mammary tissue and the trans location I-125-IGFBP-3 from the serum suggest that milk IGFBP-3 arises from the maternal circulation.