Glycodelin

Glycodelin (GD) also known as human placental protein-14 (PP-14) progestogen-associated endometrial protein (PAEP) or pregnancy-associated endometrial alpha-2 globulin is a glycoprotein that inhibits cell immune function and plays an essential role in the pregnancy process. In humans is encoded by the PAEP gene.[3][4]

PAEP
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesPAEP, GD, GdA, GdF, GdS, PAEG, PEP, PP14, progestagen associated endometrial protein, ZIF-1
External IDsOMIM: 173310 HomoloGene: 99710 GeneCards: PAEP
Orthologs
SpeciesHumanMouse
Entrez

5047

n/a

Ensembl

ENSG00000122133

n/a

UniProt

P09466

n/a

RefSeq (mRNA)

NM_001018049
NM_002571
NM_001018048

n/a

RefSeq (protein)

NP_001018058
NP_001018059
NP_002562

n/a

Location (UCSC)Chr 9: 135.56 – 135.57 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Human endometrium synthesizes several proteins under the influence of progesterone. Of these proteins, glycodelin is of particular interest. It is synthesized by the endometrial glands in the luteal phase of menstrual cycle.[5]

The temporal and spatial expression of GD in the female reproductive tract combined with its biological activities suggest that this glycoprotein probably plays an essential physiological role in the regulation of fertilization, implantation and maintenance of pregnancy.[6][7]

Structure
22 N-terminal amino acid sequence

Glycodelin is codified by 180 amino acid but it is thought that 18 of these are supposed signals peptides. The molecular weight of GD is 20,555, while its mature form is estimated to weigh 18,787. It is encoded by a 1-kilobase-pair mRNA that is expressed in human secretory endometrium and decidua but not in postmenopausal endometrium, placenta, liver, kidney, and adrenals. The four cysteinyl residues (positions 66, 106, 119, and 160) responsible for intramolecular disulfide bridges in lactoglobulins are all conserved in GD. Southern blot analysis of human DNA suggested that GD gene sequences compass some 20 kilobase pairs of the human genomic DNA.[8]

N-terminal amino acid sequence
PAEP gene structure
PAEP gene structure

The N-terminal amino acid sequence of glycodelin is M D I P Q T K Q D L E L P K L A G T W H S M. This sequence can be compared with horse, sheep, goat, bovine and buffalo beta-lactoglobulin. For example, there are 13 identities out of 22 possible matches with horse beta-lactoglobulin.

PAEP gene

This gene is a member of the kernel lipocalin superfamily whose members share relatively low sequence similarity but have highly conserved exon-intron structure and three-dimensional protein folding. The PAEP gene is clustered on the long arm of chromosome 9 and encodes for GD protein. It is mainly expressed in 60 organs, but reaches its highest expression level in the decidua.[9][10]

Function

GD is the most important protein secreted in the endometrium during the mid-luteal phase of the menstrual cycle and during the first semester of pregnancy. Four distinct forms of glycoprotein, with identical protein backbones but different glycosylation profiles, are found in amniotic fluid, follicular fluid and seminal plasma of the reproductive system. These glycoproteins have distinct and essential roles in regulating a uterine environment suitable for pregnancy and in the timing and occurrence of the appropriate sequence of events in the fertilization process.

Glycodelin-A

In the female genital tract is mainly expressed in EECs (cultured endometrial epithelial cells) and secreted into the amniotic fluid, endometrium/decidua and maternal serum. Glycodelin-A has contraceptive and immunosuppressive functions, due to the fact that suppresses Natural Killer cells, achieving the prevention of the maternal rejection of the fetus at the fetromaternal interface. It has a molecular weight of 18.78 KDa determined from the cDNA sequence.[11][12][13]

Glycodelin-S

Is secreted from seminal vesicles to the seminal fluid. A number of alternatively spliced transcript variants have been observed at this locus, but the full-length nature of only two, each encoding the same protein, has been determined. During the passage of the sperm through the cervix, glycodelin S is de-glycosylated and dissociates from the sperm, allowing the sperm to mature.[14][15][16]

Glycodelin-F

Is secreted by granulosa cells into the follicular fluid. Glycodelin-F reduces the blinding of spermatozoa to the zona pellucida which is mainly expressed in the ovary, and synthesised in the granulosa cells, has a function in principle similar to that of Glycodelin-A. It also binds the sperm head, thereby inhibiting acrosome reaction and sperm-egg binding. Upon de-glycosilation, glycodelin F dissociates from the sperm and sperm-egg binding is possible. The de-glycosilation takes place during the passage of the sperm through the corona cell layer. Glycodelin F is thereby important to prevent a premature acrosome reaction.[17][18]

Glycodelin-C

Found in Cumulus Oophorus, stimulates binding of the spermatozoa to the zona pellucida. First, cumulus cells reduce the spermatozoa-zona binding inhibitory activity of follicular fluid probably by taking up and converting glycodelin-A and glycodelin-F into glycodelin-C. Second, spermatozoa have enhanced zona bindig ability after penetrating through the cumulus oophorus. Glycodelin-C is responsible for the latter observation.[19][20]

GLYCOFORMSOURCEGLYCOSYLATIONREPRODUCTIVE FUNCTIONS
GdAAmniotic fluid, pregnancy deciduaHigh sialylation, more fucosylationImmunoprotection for implantation and placentation, antifertilizing, inhibiting spermatozoa-zona pellucida binding
GdSSeminal plasma, seminal vesiclesNo sialylated glycans, rich in fucose and mannosePreventing premature capacitation
GdFOvarian follicles, oviductFucosylated Lewis-x and Lewis-y, more N-acetylglucosamineInhibiting spermatozoa-zona pellucida, preventing premature acrosome reaction
GdCCumulus oophorus, converted from GdA and GdFReacting with specific agglutinins in lectin-binding mannerStimulating spermatozoa-zona pellucida binding

[21]

Level concentrations

PP-14 is found in the oocyte and in the sperm. In men, the concentration of this protein in seminal plasma is higher than those in serum. In women, the levels in follicular fluid exceed those of non-pregnant women.[22]

·Seminal plasma:

PP-14 is a significant protein constituent in most seminal plasma samples of men; sometimes comprising over 2.5% of the total protein content. The concentration of PP-14 in seminal plasma from men with oligospermia is in the reference range of this protein derived from values measured in normal men. However, vasectomized men concentrations are less than normal.[23]

·Women's tissues and body fluids:

In serum of non-pregnant women, the concentration of PP-14 is approximately 15-40 µg/L.

In normal pregnancy:

Location (tissues and body fluids) PP-14 concentrations (approximately) Time
Serum Up to 2200 µg/L (highest) 6–12 weeks
--- Decreasing concentrations After 16 weeks
--- 200 µg/L approx. 24 weeks (plateaued)
Amniotic fluid 232 mg/L (highest) (higher than those in maternal serum throughout pregnancy) 12–20 weeks
Cord blood 15-22 µg or undetectable ------------
Early pregnancy decidua 41–160 mg/g total protein ------------
Late pregnancy decidua 60-2700 µg/g total protein ------------
Amnion and chorion laeve From 50 to 750 µg/g protein ------------
From 50 to 1000 µg/g protein ------------
Early pregnancy placenta 0.25–15 mg/g ------------
Late pregnancy placenta 3-430 µg/g protein ------------

The concentrations of PP-14 in pregnancy serum are comparable with hCG (Human Chorionic Gonadotropin). Among all the placental proteins, the amniotic fluid PP-14 concentration is the most outstanding as decidua is a source of this protein.[24]

Future clinical applications

Placental Protein 14 has some clinical applications:

1. Biomarker of premature rupture of membranes

Premature rupture of membranes is a common pregnancy complication, taking into account that the current method does not satisfy the medical community, some researches have determined a new method: the analysis of placental protein in the maternal plasma and vaginal fluid. The results of these studies have shown that PP-14's concentration increased in the case of premature rupture of membranes. So this study conclude that PP-14 is an excellent biomarker with a sensibility of 100% and a specificity of 87,5%.[25]

2. Biomarker in in vitro fertilization process

PP-14 is known to be a great marker to predict the outcome of in vitro fertilization and the embryo transfer cycle. Some studies have shown that the serum concentration of Placental Protein 14 was highly increased after the embryo transfer cycle, and they conclude that PP-14 might be an excellent marker to predict the endometrial receptivity.[26]

References
  1. GRCh38: Ensembl release 89: ENSG00000122133 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. "PAEP - Glycodelin precursor - Homo sapiens (Human) - PAEP gene & protein". www.uniprot.org.
  4. Wang, Ping; Libho, Zhu; Xinmei, Zhang (December 2013). "The role of Placental Protein 14 in the Pathogenesis of Endometrosis". Reproductive Sciences. 20 (12): 1465–1470. doi:10.1177/1933719113488452. ISSN 0077-8923. PMC 3817670. PMID 23670949.
  5. SEPPÄLÄ, MARKKU; JULKUNEN, MERVI; KOSKIMIES, AARNE; LAATIKAINEN, TIMO; STENMAN, ULF–HÅKAN; HUHTALA, MARJA-LIISA (October 1988). "Proteins of the Human Endometrium". Annals of the New York Academy of Sciences. 541 (1): 432–444. Bibcode:1988NYASA.541..432S. doi:10.1111/j.1749-6632.1988.tb22280.x. ISSN 0077-8923. PMID 3195927. S2CID 222073546.
  6. Dutta, Binita; Mukhopadhyay, Debaditya; Roy, Nita; Das, Goutam; Karande, Anjali A. (December 1998). "Cloning, Expression, Purification, and Immunocharacterization of Placental Protein-14". Protein Expression and Purification. 14 (3): 327–334. doi:10.1006/prep.1998.0961. ISSN 1046-5928. PMID 9882566.
  7. Julkunen, M.; Seppala, M.; Janne, O. A. (1988-12-01). "Complete amino acid sequence of human placental protein 14: a progesterone-regulated uterine protein homologous to beta-lactoglobulins". Proceedings of the National Academy of Sciences. 85 (23): 8845–8849. Bibcode:1988PNAS...85.8845J. doi:10.1073/pnas.85.23.8845. ISSN 0027-8424. PMC 282603. PMID 3194393.
  8. Julkunen, M.; Seppala, M.; Janne, O. A. (1988-12-01). "Complete amino acid sequence of human placental protein 14: a progesterone-regulated uterine protein homologous to beta-lactoglobulins". Proceedings of the National Academy of Sciences. 85 (23): 8845–8849. Bibcode:1988PNAS...85.8845J. doi:10.1073/pnas.85.23.8845. ISSN 0027-8424. PMC 282603. PMID 3194393.
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  12. Kao, L. C.; Tulac, S.; Lobo, S.; Imani, B.; Yang, J. P.; Germeyer, A.; Osteen, K.; Taylor, R. N.; Lessey, B. A.; Giudice, L. C. (June 2002). "Global Gene Profiling in Human Endometrium during the Window of Implantation". Endocrinology. 143 (6): 2119–2138. doi:10.1210/endo.143.6.8885. ISSN 0013-7227. PMID 12021176.
  13. Alok, Anshula; Mukhopadhyay, Debaditya; Karande, Anjali A. (May 2009). "Glycodelin A, an immunomodulatory protein in the endometrium, inhibits proliferation and induces apoptosis in monocytic cells". The International Journal of Biochemistry & Cell Biology. 41 (5): 1138–1147. doi:10.1016/j.biocel.2008.10.009. ISSN 1357-2725. PMID 18996219.
  14. Mandelin, Erik; Koistinen, Hannu; Koistinen, Riitta; Arola, Johanna; Affandi, Biran; Seppälä, Markku (September 2001). "Endometrial expression of glycodelin in women with levonorgestrel-releasing subdermal implants". Fertility and Sterility. 76 (3): 474–478. doi:10.1016/s0015-0282(01)01969-0. ISSN 0015-0282. PMID 11532467.
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  16. Koistinen, Hannu; Koistinen, Riitta; Dell, Anne; Morris, Howard R.; Easton, Richard L.; Patankar, Manish S.; Oehninger, Sergio; Clark, Gary F.; Seppälä, Markku (1996). "Glycodelin from seminal plasma is a differentially glycosylated form of contraceptive glycodelin-A". Molecular Human Reproduction. 2 (10): 759–765. doi:10.1093/molehr/2.10.759. ISSN 1360-9947. PMID 9239694.
  17. Chiu, Philip C. N.; Chung, Man-Kin; Koistinen, Riitta; Koistinen, Hannu; Seppala, Markku; Ho, Pak-Chung; Ng, Ernest H. Y.; Lee, Kai-Fai; Yeung, William S. B. (2006-12-27). "Cumulus Oophorus-associated Glycodelin-C Displaces Sperm-bound Glycodelin-A and -F and Stimulates Spermatozoa-Zona Pellucida Binding". Journal of Biological Chemistry. 282 (8): 5378–5388. doi:10.1074/jbc.m607482200. ISSN 0021-9258. PMID 17192260.
  18. Kölbl, Alexandra C.; Andergassen, Ulrich; Jeschke, Udo (2015-10-13). "The Role of Glycosylation in Breast Cancer Metastasis and Cancer Control". Frontiers in Oncology. 5: 219. doi:10.3389/fonc.2015.00219. ISSN 2234-943X. PMC 4602128. PMID 26528431.
  19. Chiu, Philip C. N.; Chung, Man-Kin; Koistinen, Riitta; Koistinen, Hannu; Seppala, Markku; Ho, Pak-Chung; Ng, Ernest H. Y.; Lee, Kai-Fai; Yeung, William S. B. (2006-12-27). "Cumulus Oophorus-associated Glycodelin-C Displaces Sperm-bound Glycodelin-A and -F and Stimulates Spermatozoa-Zona Pellucida Binding". Journal of Biological Chemistry. 282 (8): 5378–5388. doi:10.1074/jbc.m607482200. ISSN 0021-9258. PMID 17192260.
  20. Yeung, William S.B.; Lee, Kai-Fai; Koistinen, Riitta; Koistinen, Hannu; Seppälä, Markku; Chiu, Philip C.N. (December 2009). "Effects of glycodelins on functional competence of spermatozoa". Journal of Reproductive Immunology. 83 (1–2): 26–30. doi:10.1016/j.jri.2009.04.012. ISSN 0165-0378. PMID 19857900.
  21. Cui, Juan; Liu, Yanguo; Wang, Xiuwen (2017-11-29). "The Roles of Glycodelin in Cancer Development and Progression". Frontiers in Immunology. 8: 1685. doi:10.3389/fimmu.2017.01685. ISSN 1664-3224. PMC 5712544. PMID 29238349.
  22. SEPPäLä, MARKKU; KOSKIMIES, AARNE I.; TENHUNEN, ANSSI; RUTANEN, EEVA-MARJA; SJÖBERG, JARI; KOISTINEN, RIITTA; JULKUNEN, MERVI; WAHLSTRÖM, TORSTEN (May 1985). "Pregnancy Proteins in Seminal Plasma, Seminal Vesicles, Preovulatory Follicular Fluid, and Ovary". Annals of the New York Academy of Sciences. 442 (1 In Vitro Fert): 212–226. Bibcode:1985NYASA.442..212S. doi:10.1111/j.1749-6632.1985.tb37522.x. ISSN 0077-8923. PMID 3893267. S2CID 11729995.
  23. Bolton, A. E.; Pinto-Furtado, L. G.; Andrew, C. E.; Chapman, M. G. (June 1986). "Measurement of the pregnancy-associated proteins, placental protein 14 and pregnancy-associated plasma protein A in human seminal plasma". Clinical Reproduction and Fertility. 4 (3): 233–240. ISSN 0725-556X. PMID 2427179.
  24. JULKUNEN, MERVI; RUTANEN, EEVA-MARJA; KOSKIMIES, AARNE; RANTA, TAPIO; BOHN, HANS; SEPPALA, MARKKU (November 1985). "Distribution of placental protein 14 in tissues and body fluids during pregnancy". BJOG: An International Journal of Obstetrics and Gynaecology. 92 (11): 1145–1151. doi:10.1111/j.1471-0528.1985.tb03027.x. ISSN 1470-0328. PMID 4063232. S2CID 40266453.
  25. Yanyun , Haibo, Guanglu, Yanqin, Jun, Qiongli,Qiongli, Linbo ,Tao, Wang, Luo, Che, Li, Gao,Yang, Zhou, Gao, Wang. (2018). "Placental protein 14 as a potential biomarker for diagnosis of preterm premature rupture of membranes". Molecular Medicine Reports. 18 (1): 113–122. doi:10.3892/mmr.2018.8967. PMC 6059659. PMID 29749501. Retrieved 25 October 2019.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  26. Suzuki, Fukumine, Sugiyama, Usuda, Yoshichika, Noritaka, Rikikazu, Saburo. (2000). "Clinical Applications of Serum Placental Protein 14 (PP14) Measurement in the IVF-ET Cycle". Journal of Obstetrics and Gynaecology Research. 26 (4): 295–302. doi:10.1111/j.1447-0756.2000.tb01325.x. PMID 11049241. S2CID 22904564. Retrieved 25 October 2019.{{cite journal}}: CS1 maint: multiple names: authors list (link)

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