Literature DB >> 3136004

Estrogen regulation of the central enzymes involved in O- and N-linked glycoprotein assembly in the developing and the adult rabbit endocervix.

B S Chilton1, H A Kaplan, W J Lennarz.   

Abstract

During cervical differentiation in 1- to 6-month-old rabbits, a marked increase was observed in the titer of serum estradiol, the number of secretory cells in the endocervix, and the granule content of these cells. Because these secretory granules are rich in carbohydrates it seemed likely that hormones regulate glycoconjugate biosynthesis in the endocervix. To investigate this possibility, the synthesis of O- and N-linked glycoproteins was studied in cell-free preparations from endocervical epithelium. The activity of N-acetylgalactosaminyl (GalNAc) transferase, the first enzyme in the pathway for O-linked oligosaccharide chain biosynthesis, measured in microsomes prepared from the developing cervix, was increased 8-fold. Oligosaccharyltransferase, the enzyme that catalyzes the first step in the attachment of N-linked oligosaccharide chains to proteins, was measured in microsomes prepared under the same conditions as those used for GalNAc transferase. The results of two independent assay methods revealed an estrogen-dependent 10- to 15-fold increase in oligosaccharyltransferase during cervical differentiation. Consistent with these developmental effects, ovariectomy of adult rabbits resulted in reduced (P less than 0.01) titers of serum estradiol and a 2-fold reduction in the specific activity of GalNAc transferase. When animals were treated with exogenous estradiol, GalNAc transferase activity returned to estrous control levels. The antagonistic action of progesterone on GalNAc transferase activity was verified using endocervical membranes from pseudopregnant animals. Similarly, oligosaccharyltransferase activity was reduced 2- to 3-fold when estrous animals were ovariectomized or made pseudopregnant. The treatment of ovariectomized animals with estradiol resulted in the restoration of oligosaccharyltransferase to estrous control values. Collectively, these results provide the first definitive evidence that hormones can regulate the activity of the enzymes involved in the attachment of O- and N-linked oligosaccharide chains to proteins in the endocervix.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3136004     DOI: 10.1210/endo-123-3-1237

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  5 in total

1.  Cellular and viral components that mediate glucocorticoid-regulated processing of retroviral envelope proteins.

Authors:  M R Stallcup; J L Corey; R M Bedgood
Journal:  Cell Biophys       Date:  1991 Oct-Dec

2.  Glycosylation site-binding protein is not required for N-linked glycoprotein synthesis.

Authors:  R Noiva; H A Kaplan; W J Lennarz
Journal:  Proc Natl Acad Sci U S A       Date:  1991-03-01       Impact factor: 11.205

3.  O-glycosylation of α-1-acid glycoprotein of human milk is lactation stage related.

Authors:  Magdalena Orczyk-Pawiłowicz; Marta Berghausen-Mazur; Lidia Hirnle; Iwona Kątnik-Prastowska
Journal:  Breastfeed Med       Date:  2015-06       Impact factor: 1.817

4.  N-linked glycan profiling of mature human milk by high-performance microfluidic chip liquid chromatography time-of-flight tandem mass spectrometry.

Authors:  David C Dallas; William F Martin; John S Strum; Angela M Zivkovic; Jennifer T Smilowitz; Mark A Underwood; Michael Affolter; Carlito B Lebrilla; J Bruce German
Journal:  J Agric Food Chem       Date:  2011-03-18       Impact factor: 5.279

5.  The order of processing events in mouse mammary tumor virus envelope protein maturation: implications for the location of the glucocorticoid-regulated step.

Authors:  J L Corey; M R Stallcup
Journal:  Cell Regul       Date:  1990-06
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.