Literature DB >> 26109616

Altered β1,6-GlcNAc and bisecting GlcNAc-branched N-glycan on integrin β1 are associated with early spontaneous miscarriage in humans.

Min Zhang1, Meirong Wang1, Rufei Gao1, Xueqing Liu1, Xuemei Chen1, Yanqing Geng1, Yubin Ding1, Yingxiong Wang1, Junlin He2.   

Abstract

STUDY QUESTION: Do N-acetylglucosaminyltransferase (GnT-V) and N-acetylglucosaminyltransferase III (GnT-III) play an important role in early spontaneous miscarriage (ESM) in humans. SUMMARY ANSWER: The dynamic balance between GnT-V and GnT-III expression in chorionic villi differed between early normal pregnancy and ESM and was associated with altered β1,6-N-acetylglucosamine (β1,6-GlcNAc) and bisecting N-acetylglucosamine (bis-GlcNAc) branched N-glycans on integrin β1. WHAT IS KNOWN ALREADY: GnT-V contributes to metastasis, while GnT-III is recognized as a metastasis suppressor. It has been reported that GnT-V contributes to placentation in the early phase of pregnancy, possibly regulating trophoblast invasion. However, the expressions of GnT-V and GnT-III in ESM have not been reported. STUDY DESIGN, SIZE, DURATION: Villous samples from 6 to 9 weeks of gestation were collected in the First Affiliated Hospital of Chongqing Medical University from May 2013 to September 2014 from 60 normal pregnant women undergoing elective termination of pregnancy and from 40 patients with a clinical diagnosis of ESM. PARTICIPANTS, MATERIALS, SETTING,
METHODS: Quantitative PCR and western blots were used to examine the GnT-V and GnT-III mRNA (Mgat5 and Mgat3) and protein expression, respectively, of chorionic villi in both the ESM group and the normal group from week 6 to week 9. We used immunofluorescence and immunohistochemistry to detect the location of GnT-V and GnT-III. Lectin fluorescence and histochemistry were used to test the location of β1,6-GlcNAc and bis-GlcNAc branching in the normal and ESM groups. To assess the functional capacity of GnT-V and GnT-III in the chorionic villi between the two groups, we used an enzyme-linked immunosorbent assay kit to measure the activity of these enzymes. Using co-precipitated integrin α5β1 followed by phytohaemagglutinin (PHA)-L and PHA-E blotting, we investigated whether GnT-V and GnT-III could modify the N-glycosylation profile in terms of the β1,6-GlcNAc and bis-GlcNAc structures in integrin α5β1 during the first trimester in both groups. MAIN RESULTS AND THE ROLE OF CHANCE: In the normal group expression and activity of GnT-V and the concentration of its product, β1,6-GlcNAc were higher at week 9 than at weeks 6, 7 and 8 (P < 0.05). In contrast, the expression and activity of GnT-III and the concentration of its product, bis-GlcNAc were higher at week 6 than at weeks 7, 8 and 9 (P < 0.05). Compared with the normal group, the ESM group exhibited a lower expression of GnT-V and β1,6-GlcNAc (P < 0.05) and a higher expression of GnT-III and bis-GlcNAc (P < 0.05) with consistent changes in enzymatic activity. Immunofluorescence showed that GnT-V was located mainly in the cytoplasm of syncytiotrophoblasts (STBs) and chorionic villous cytotrophoblasts (CTBs), in both the ESM group and the normal group. β1,6-GlcNAc N-glycan was mainly located outside of the STB and CTB layer in normal villi and was expressed only rarely in the ESM villi. GnT-III was expressed primarily in the cytoplasm of STBs and expressed only very weakly in the CTBs of normal villi, whereas it was highly expressed in both the STBs and CTBs in the ESM group. bis-GlcNAc was primarily located outside of the STBs in the normal villi, whereas it was expressed much more abundantly outside of both the STBs and CTBs in the ESM group at each week of gestation. Moreover, decreased β1,6-GlcNAc-branched N-glycans and increased bis-GlcNAc-branched N-glycans on integrin β1 (P < 0.05) were observed in the ESM group. WIDER IMPLICATIONS OF THE
FINDINGS: Our findings provide a new insight for studying the mechanism of clinical ESM in humans and it might be valuable for the clinical diagnosis and treatment of ESM. LIMITATIONS, REASONS FOR CAUTION: The study lacks experiments in vitro to disclose the precise mechanism by which GnT-V and GnT-III regulate ESM. In some cases, degradation of the tissues after the miscarriage event cannot be ruled out. STUDY FUNDING/COMPETING INTERESTS: This study was supported by grants from the National Natural Science Foundation of China (31271546). The authors have no competing interests.
© The Author 2015. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  GnT-III; GnT-V; early spontaneous miscarriage; glycosylation; integrin

Mesh:

Substances:

Year:  2015        PMID: 26109616     DOI: 10.1093/humrep/dev153

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  9 in total

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Authors:  Enoch Appiah Adu-Gyamfi; Armin Czika; Philip Narteh Gorleku; Amin Ullah; Zulqarnain Panhwar; Ling-Ling Ruan; Yu-Bin Ding; Ying-Xiong Wang
Journal:  Reprod Sci       Date:  2020-11-04       Impact factor: 3.060

2.  Glycan characterization of pregnancy-specific glycoprotein 1 and its identification as a novel Galectin-1 ligand.

Authors:  Mirian Mendoza; Dongli Lu; Angela Ballesteros; Sandra M Blois; Kelsey Abernathy; Chiguang Feng; Charles J Dimitroff; Jonathan Zmuda; Maria Panico; Anne Dell; Gerardo R Vasta; Stuart M Haslam; Gabriela Dveksler
Journal:  Glycobiology       Date:  2020-10-21       Impact factor: 4.313

Review 3.  Functional glycosylation in the human and mammalian uterus.

Authors:  Gary F Clark
Journal:  Fertil Res Pract       Date:  2015-10-23

Review 4.  The Essential Functions and Detection of Bisecting GlcNAc in Cell Biology.

Authors:  Qiushi Chen; Zengqi Tan; Feng Guan; Yan Ren
Journal:  Front Chem       Date:  2020-07-03       Impact factor: 5.221

Review 5.  Pregnancy Galectinology: Insights Into a Complex Network of Glycan Binding Proteins.

Authors:  Sandra M Blois; Gabriela Dveksler; Gerardo R Vasta; Nancy Freitag; Véronique Blanchard; Gabriela Barrientos
Journal:  Front Immunol       Date:  2019-05-29       Impact factor: 7.561

Review 6.  Role of galectin-glycan circuits in reproduction: from healthy pregnancy to preterm birth (PTB).

Authors:  Sandra M Blois; Stefan Verlohren; Gang Wu; Gary Clark; Anne Dell; Stuart M Haslam; Gabriela Barrientos
Journal:  Semin Immunopathol       Date:  2020-06-29       Impact factor: 9.623

Review 7.  The Immunology of Syncytialized Trophoblast.

Authors:  Danny J Schust; Elizabeth A Bonney; Jun Sugimoto; Toshi Ezashi; R Michael Roberts; Sehee Choi; Jie Zhou
Journal:  Int J Mol Sci       Date:  2021-02-10       Impact factor: 6.208

8.  Altered Glycosylation Contributes to Placental Dysfunction Upon Early Disruption of the NK Cell-DC Dynamics.

Authors:  Sophia Borowski; Irene Tirado-Gonzalez; Nancy Freitag; Mariana G Garcia; Gabriela Barrientos; Sandra M Blois
Journal:  Front Immunol       Date:  2020-07-14       Impact factor: 7.561

9.  EIF5A1 promotes trophoblast migration and invasion via ARAF-mediated activation of the integrin/ERK signaling pathway.

Authors:  Jing Zhang; Hui-Qin Mo; Fu-Ju Tian; Wei-Hong Zeng; Xiao-Rui Liu; Xiao-Ling Ma; Xiao Li; Shi Qin; Cui-Fang Fan; Yi Lin
Journal:  Cell Death Dis       Date:  2018-09-11       Impact factor: 8.469

  9 in total

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