Proliferation of endoplasmic reticulum with its enzyme, UDP- glucuronyltransferase, in chick embryo liver during culture. Effects of phenobarbital

UDP-Glucuronyltransferase (GT) activity increases in chick embryo liver during culture from zero to a steady-state level at or above adult values. The GT activity (o-aminophenol as acceptor) is located entirely in the membranes of the endoplasmic reticulum (ER) and the question arises whether ER increases along with GT. Earlier work showed that the synthesis and degradation rates of GT can be varied in culture over wide ranges by choosing embryo livers of different ages and both phenobarbital. In the present study we measured the GT activities and the concentrations of ER (using stereologic methods) in 5- and 11-day embryo liver during culture with and without phenobarbital. We found that GT and ER always increased in a constant ratio of 2.2 X 10(-9) U of GR activity per square micrometer of membrane, suggesting that the synthesis and degradation of GT are coupled to the synthesis and degradation of ER. A general structure for ER is proposed to explain this finding.

[1]  C. A. Benzo,et al.  Development of chick embryo liver during organ culture: Requirement for zinc‐insulin , 1972, Journal of cellular physiology.

[2]  C. A. Benzo,et al.  FACTORS CONTROLLING DEVELOPMENT OF CHICK EMBRYO LIVER CELLS DURING ORGAN CULTURE , 1971, The Journal of cell biology.

[3]  B. Trump,et al.  Membrane structure: lipid-protein interactions in microsomal membranes. , 1970, Proceedings of the National Academy of Sciences of the United States of America.

[4]  B. Skea,et al.  Factors influencing premature induction of UDP-glucuronyltransferase activity in cultured chick embryo liver cells. , 1969, Proceedings of the National Academy of Sciences of the United States of America.

[5]  J. Fouts,et al.  The submicrosomal distribution of hepatic uridine diphosphate glucuronyltransferases in the rabbit. , 1968, The Biochemical journal.

[6]  Anastasia J. Romanoff,et al.  Biochemistry of the Avian Embryo , 1967 .

[7]  P. Siekevitz,et al.  BIOGENESIS OF ENDOPLASMIC RETICULUM MEMBRANES , 1966, The Journal of cell biology.

[8]  P. Siekevitz,et al.  BIOGENESIS OF ENDOPLASMIC RETICULUM MEMBRANES , 1966, The Journal of cell biology.

[9]  Mollenhauer Hh PLASTIC EMBEDDING MIXTURES FOR USE IN ELECTRON MICROSCOPY. , 1964 .

[10]  A. Loud A METHOD FOR THE QUANTITATIVE ESTIMATION OF CYTOPLASMIC STRUCTURES , 1962, The Journal of cell biology.

[11]  P. Broughton A rapid ultraviolet spectrophotometric method for the detection, estimation and identification of barbiturates in biological material. , 1956, The Biochemical journal.

[12]  A. Dalton,et al.  The functional differentiation of the hepatic cells of the chick embryo , 1937 .

[13]  A. J. Dalton,et al.  The ontogenetic history of the mitochondria and Golgi network of the hepatic cell of the chick , 1934 .

[14]  S J Singer,et al.  The molecular organization of membranes. , 1974, Annual review of biochemistry.

[15]  A. M. Nemeth The regulation of liver development by birth. , 1973, Enzyme.

[16]  Nemeth Am The regulation of liver development by birth. , 1973 .

[17]  M. Karnovsky,et al.  A formaldehyde-glutaraldehyde fixative of high osmolality for use in electron-microscopy , 1965 .

[18]  H. Mollenhauer PLASTIC EMBEDDING MIXTURES FOR USE IN ELECTRON MICROSCOPY. , 1964, Stain technology.

[19]  G. Dutton,et al.  Glucuronide synthesis in foetal liver and other tissues. , 1959, The Biochemical journal.