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Albumin and transferrin synthesis during development in the rat
The Biochemical Journal
|November 1, 1974
Summary
Albumin and transferrin synthesis in rat fetuses and neonates was investigated. Transferrin synthesis began later than albumin synthesis, with differing rates and serum concentrations suggesting developmental regulation and protein stability play key roles.
Area of Science:
- Developmental Biology
- Biochemistry
- Proteomics
Background:
- Plasma proteins like albumin and transferrin are crucial for fetal and postnatal development.
- Understanding their synthesis rates and regulation provides insights into developmental processes.
Purpose of the Study:
- To compare the synthesis rates of albumin and transferrin during rat development.
- To investigate the expression of these proteins in fetal tissues and perinatal liver.
- To correlate synthesis rates with serum concentrations and explore discrepancies.
Main Methods:
- [(14)C]leucine incorporation was used to measure albumin and transferrin synthesis rates.
- Synthesis was assessed in fetal tissues (fetuses, membranes, placenta) and perinatal liver slices.
- Serum concentrations of albumin and transferrin were determined at different developmental stages.
Main Results:
- Albumin synthesis detected from day 13 gestation; transferrin synthesis from day 15.
- Transferrin synthesis occurred in membranes but not placenta; liver synthesis increased with age postnatally.
- Fetuses showed higher relative transferrin than albumin synthesis compared to postnatal animals.
- Serum protein concentrations increased before term while synthesis declined; postnatal changes showed discrepancies with synthesis rates.
Conclusions:
- Differential timing of albumin and transferrin synthesis suggests distinct developmental regulation.
- Postnatal discrepancies between synthesis and serum levels may be due to increased protein stability and uptake by non-synthesizing cells (e.g., liver hematopoietic cells).
- Developmental changes in protein stability and cellular uptake influence circulating levels of albumin and transferrin.