Abstract

A sensitive DNA-excess solution hybridization assay was used to quantitate apo-E mRNA in the liver and peripheral tissues of two nonhuman primates, Macaca fascicularis and Cercopithecus aethiops. When expressed on the basis of total RNA, apo-E mRNA values for M. fascicularis adrenal, brain, testis, and spleen ranged from 17-52% of the liver value. Apo-E mRNA values for mesenteric lymph node, kidney, thymus, and skeletal muscle were 1-5% of the liver value. When expressed on a cellular basis, apo-E mRNA was most abundant in the liver at approximately 1200 molecules/cell. Peripheral tissues showed a continuous range of apo-E mRNA from 1.5 molecules/cell in the thymus up to 350 molecules/cell in the brain. Similar results were obtained with peripheral tissues from C. aethiops in which case apo-E mRNA also was found in skin, lung, skeletal muscle, small intestine, and vascular tissues such as heart, aorta, and brachial artery. Calculation of the total apo-E mRNA/organ showed that most of the apo-E mRNA was present in the liver. However, summation of apo-E mRNA in peripheral tissues indicated that 20-40% of total body apo-E mRNA was extrahepatic. This results indicates that apo-E made in peripheral tissues may play a quantitatively important role in cholesterol metabolism since peripheral tissues have the potential to contribute a significant fraction of plasma apo-E.

Highlights

  • Measurements of relative synthetic rates show that apo-E is an abundant protein product in many tissoufensonhuman primates (6)

  • The probe was component of the reverse cholesterol transport system which examined intwo ways to ensure thatwiats highly homologous serves to transportcholesterol from peripheral tissues to the to monkey apo-E mRNA

  • Whether expressed in terms of total RNA or as molecules/cell, it is clear that apo-E mRNA is presentin high amounts in numerousperipheral tissues

Read more

Summary

RESULTS

Metabolism as a recognition signal for the hepatic clearance Hybridization Assay-Apo-E mRNA in the liver and peof cholesteryl ester-enriched chylomicron remnants andhigh ripheral tissues of the monkey was measuredwithaDNA density lipoprotein subfractions (1-4). The probe was component of the reverse cholesterol transport system which examined intwo ways to ensure thatwiats highly homologous serves to transportcholesterol from peripheral tissues to the to monkey apo-E mRNA. Apo-E is synthesized by mouse peritoneal macrophages (7) and human peripherabllood monanalysis under stringent conditionwsas carried outwith RNA from human HepG2 hepatoma cells and cynomolgus monkey liver. Full size photocopies are available fromthe Journal of Biological Chemistry, 9650 Rockville Pike, Bethesda, MD 20814. Full size photocopies are included in the microfilm edition of the Journal acetic acid.

E Messenger RNA
RNA or monkey
RNAprepared from cultureRd hesus
Findings
DISCUSSION
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call