Loading…

Lectin histochemistry for detecting cadmium-induced changes in the glycosylation pattern of rat placenta

Cadmium (Cd) is an industrial and environmental pollutant that produces toxic effects on gametogenesis, pre- and post-implantation embryos, and the placenta. Because the effects of acute Cd intoxication on the placenta are not well understood, we investigated changes in its glycosylated components i...

Full description

Saved in:
Bibliographic Details
Published in:Biotechnic & histochemistry 2017-01, Vol.92 (1), p.36-45
Main Authors: Díaz, MC, González, NV, Zanuzzi, CN, Najle, R, Barbeito, CG
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c366t-925da53310261195d37b49cd216c441c2498e506c430c7ad239f9554989a67923
cites cdi_FETCH-LOGICAL-c366t-925da53310261195d37b49cd216c441c2498e506c430c7ad239f9554989a67923
container_end_page 45
container_issue 1
container_start_page 36
container_title Biotechnic & histochemistry
container_volume 92
creator Díaz, MC
González, NV
Zanuzzi, CN
Najle, R
Barbeito, CG
description Cadmium (Cd) is an industrial and environmental pollutant that produces toxic effects on gametogenesis, pre- and post-implantation embryos, and the placenta. Because the effects of acute Cd intoxication on the placenta are not well understood, we investigated changes in its glycosylated components in Cd treated dams at days 4, 7, 10 and 15 of gestation using lectin histochemistry. CdCl 2 was administered to pregnant rats; control animals received sterile normal saline. Placentas were processed for DBA, Con A, SBA, PNA, UEA-I, RCA-I and WGA lectin histochemistry to evaluate changes in the carbohydrate pattern of the placenta that might modify cell interactions and contribute to embryonic alterations. Lectin binding was analyzed in the yolk sac; trophoblast giant cells; trophoblast I, II and III; spongiotrophoblast cells and endovascular trophoblast cells in the chorioallantoic placenta. Our lectin binding patterns showed that Cd caused alteration of SBA and DBA labeling of trophoblast-derived cells, which suggested increased expressions of α and β GalNAc. Cd also caused decreased UEA-1 binding affinity, which indicated fewer α-L-Fuc residues in placentas of Cd treated dams. The nonreactivity in trophoblast I of the control placentas incubated with Con-A contrasted with the labeling in placentas of experimental dams, which indicated increased expression of terminal α-D-Man, and α-D-Glc residues. We found that Cd altered the reactivity of placenta to several lectins, which indicated modification of the glycotype presented by the fetal component of the placenta. We report that Cd exerts a deleterious effect on the glycosylation pattern of the placenta.
doi_str_mv 10.1080/10520295.2016.1185668
format article
fullrecord <record><control><sourceid>pubmed_infor</sourceid><recordid>TN_cdi_pubmed_primary_28166424</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>28166424</sourcerecordid><originalsourceid>FETCH-LOGICAL-c366t-925da53310261195d37b49cd216c441c2498e506c430c7ad239f9554989a67923</originalsourceid><addsrcrecordid>eNp9kMlOwzAURS0EoqXwCSD_QIqH2Il3oIpJqsQG1pZrO41R4kS2K5S_x6UtS1b3Dfe-Jx0AbjFaYlSje4wYQUSwJUGYLzGuGef1GZjjsqJFVXF0nuvsKfamGbiK8QshVNUCX4IZqTHnJSnnoF1bnZyHrYtp0K3ts4YJNkOAxqbf3RZqZXq36wvnzU5bA3Wr_NZGmHOptXDbTXqIU6eSGzwcVUo2eDg0MKgEx05p65O6BheN6qK9OeoCfD4_faxei_X7y9vqcV1oynkqBGFGMUoxIhxjwQytNqXQhmCuyxJrUoraMpQbinSlDKGiEYzlqVC8EoQuADvc1WGIMdhGjsH1KkwSI7knJ0_k5J6cPJLLubtDbtxtemv-UidU2fBwMDif6fTqewidkUlN3RCaoLx2UdL_f_wApbx9vQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Lectin histochemistry for detecting cadmium-induced changes in the glycosylation pattern of rat placenta</title><source>Taylor and Francis Science and Technology Collection</source><creator>Díaz, MC ; González, NV ; Zanuzzi, CN ; Najle, R ; Barbeito, CG</creator><creatorcontrib>Díaz, MC ; González, NV ; Zanuzzi, CN ; Najle, R ; Barbeito, CG</creatorcontrib><description>Cadmium (Cd) is an industrial and environmental pollutant that produces toxic effects on gametogenesis, pre- and post-implantation embryos, and the placenta. Because the effects of acute Cd intoxication on the placenta are not well understood, we investigated changes in its glycosylated components in Cd treated dams at days 4, 7, 10 and 15 of gestation using lectin histochemistry. CdCl 2 was administered to pregnant rats; control animals received sterile normal saline. Placentas were processed for DBA, Con A, SBA, PNA, UEA-I, RCA-I and WGA lectin histochemistry to evaluate changes in the carbohydrate pattern of the placenta that might modify cell interactions and contribute to embryonic alterations. Lectin binding was analyzed in the yolk sac; trophoblast giant cells; trophoblast I, II and III; spongiotrophoblast cells and endovascular trophoblast cells in the chorioallantoic placenta. Our lectin binding patterns showed that Cd caused alteration of SBA and DBA labeling of trophoblast-derived cells, which suggested increased expressions of α and β GalNAc. Cd also caused decreased UEA-1 binding affinity, which indicated fewer α-L-Fuc residues in placentas of Cd treated dams. The nonreactivity in trophoblast I of the control placentas incubated with Con-A contrasted with the labeling in placentas of experimental dams, which indicated increased expression of terminal α-D-Man, and α-D-Glc residues. We found that Cd altered the reactivity of placenta to several lectins, which indicated modification of the glycotype presented by the fetal component of the placenta. We report that Cd exerts a deleterious effect on the glycosylation pattern of the placenta.</description><identifier>ISSN: 1052-0295</identifier><identifier>EISSN: 1473-7760</identifier><identifier>DOI: 10.1080/10520295.2016.1185668</identifier><identifier>PMID: 28166424</identifier><language>eng</language><publisher>England: Taylor &amp; Francis</publisher><subject>Animals ; cadmium ; Cadmium - toxicity ; carbohydrate moieties ; Female ; glycoproteins ; Glycosylation ; lectin histochemistry ; Lectins - chemistry ; placenta ; Placenta - drug effects ; Placenta - metabolism ; Pregnancy ; rat ; Rats ; Rats, Wistar ; Trophoblasts - drug effects ; Trophoblasts - physiology</subject><ispartof>Biotechnic &amp; histochemistry, 2017-01, Vol.92 (1), p.36-45</ispartof><rights>2017 The Biological Stain Commission 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c366t-925da53310261195d37b49cd216c441c2498e506c430c7ad239f9554989a67923</citedby><cites>FETCH-LOGICAL-c366t-925da53310261195d37b49cd216c441c2498e506c430c7ad239f9554989a67923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28166424$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Díaz, MC</creatorcontrib><creatorcontrib>González, NV</creatorcontrib><creatorcontrib>Zanuzzi, CN</creatorcontrib><creatorcontrib>Najle, R</creatorcontrib><creatorcontrib>Barbeito, CG</creatorcontrib><title>Lectin histochemistry for detecting cadmium-induced changes in the glycosylation pattern of rat placenta</title><title>Biotechnic &amp; histochemistry</title><addtitle>Biotech Histochem</addtitle><description>Cadmium (Cd) is an industrial and environmental pollutant that produces toxic effects on gametogenesis, pre- and post-implantation embryos, and the placenta. Because the effects of acute Cd intoxication on the placenta are not well understood, we investigated changes in its glycosylated components in Cd treated dams at days 4, 7, 10 and 15 of gestation using lectin histochemistry. CdCl 2 was administered to pregnant rats; control animals received sterile normal saline. Placentas were processed for DBA, Con A, SBA, PNA, UEA-I, RCA-I and WGA lectin histochemistry to evaluate changes in the carbohydrate pattern of the placenta that might modify cell interactions and contribute to embryonic alterations. Lectin binding was analyzed in the yolk sac; trophoblast giant cells; trophoblast I, II and III; spongiotrophoblast cells and endovascular trophoblast cells in the chorioallantoic placenta. Our lectin binding patterns showed that Cd caused alteration of SBA and DBA labeling of trophoblast-derived cells, which suggested increased expressions of α and β GalNAc. Cd also caused decreased UEA-1 binding affinity, which indicated fewer α-L-Fuc residues in placentas of Cd treated dams. The nonreactivity in trophoblast I of the control placentas incubated with Con-A contrasted with the labeling in placentas of experimental dams, which indicated increased expression of terminal α-D-Man, and α-D-Glc residues. We found that Cd altered the reactivity of placenta to several lectins, which indicated modification of the glycotype presented by the fetal component of the placenta. We report that Cd exerts a deleterious effect on the glycosylation pattern of the placenta.</description><subject>Animals</subject><subject>cadmium</subject><subject>Cadmium - toxicity</subject><subject>carbohydrate moieties</subject><subject>Female</subject><subject>glycoproteins</subject><subject>Glycosylation</subject><subject>lectin histochemistry</subject><subject>Lectins - chemistry</subject><subject>placenta</subject><subject>Placenta - drug effects</subject><subject>Placenta - metabolism</subject><subject>Pregnancy</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Trophoblasts - drug effects</subject><subject>Trophoblasts - physiology</subject><issn>1052-0295</issn><issn>1473-7760</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kMlOwzAURS0EoqXwCSD_QIqH2Il3oIpJqsQG1pZrO41R4kS2K5S_x6UtS1b3Dfe-Jx0AbjFaYlSje4wYQUSwJUGYLzGuGef1GZjjsqJFVXF0nuvsKfamGbiK8QshVNUCX4IZqTHnJSnnoF1bnZyHrYtp0K3ts4YJNkOAxqbf3RZqZXq36wvnzU5bA3Wr_NZGmHOptXDbTXqIU6eSGzwcVUo2eDg0MKgEx05p65O6BheN6qK9OeoCfD4_faxei_X7y9vqcV1oynkqBGFGMUoxIhxjwQytNqXQhmCuyxJrUoraMpQbinSlDKGiEYzlqVC8EoQuADvc1WGIMdhGjsH1KkwSI7knJ0_k5J6cPJLLubtDbtxtemv-UidU2fBwMDif6fTqewidkUlN3RCaoLx2UdL_f_wApbx9vQ</recordid><startdate>20170102</startdate><enddate>20170102</enddate><creator>Díaz, MC</creator><creator>González, NV</creator><creator>Zanuzzi, CN</creator><creator>Najle, R</creator><creator>Barbeito, CG</creator><general>Taylor &amp; Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20170102</creationdate><title>Lectin histochemistry for detecting cadmium-induced changes in the glycosylation pattern of rat placenta</title><author>Díaz, MC ; González, NV ; Zanuzzi, CN ; Najle, R ; Barbeito, CG</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c366t-925da53310261195d37b49cd216c441c2498e506c430c7ad239f9554989a67923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>cadmium</topic><topic>Cadmium - toxicity</topic><topic>carbohydrate moieties</topic><topic>Female</topic><topic>glycoproteins</topic><topic>Glycosylation</topic><topic>lectin histochemistry</topic><topic>Lectins - chemistry</topic><topic>placenta</topic><topic>Placenta - drug effects</topic><topic>Placenta - metabolism</topic><topic>Pregnancy</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Trophoblasts - drug effects</topic><topic>Trophoblasts - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Díaz, MC</creatorcontrib><creatorcontrib>González, NV</creatorcontrib><creatorcontrib>Zanuzzi, CN</creatorcontrib><creatorcontrib>Najle, R</creatorcontrib><creatorcontrib>Barbeito, CG</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Biotechnic &amp; histochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Díaz, MC</au><au>González, NV</au><au>Zanuzzi, CN</au><au>Najle, R</au><au>Barbeito, CG</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lectin histochemistry for detecting cadmium-induced changes in the glycosylation pattern of rat placenta</atitle><jtitle>Biotechnic &amp; histochemistry</jtitle><addtitle>Biotech Histochem</addtitle><date>2017-01-02</date><risdate>2017</risdate><volume>92</volume><issue>1</issue><spage>36</spage><epage>45</epage><pages>36-45</pages><issn>1052-0295</issn><eissn>1473-7760</eissn><abstract>Cadmium (Cd) is an industrial and environmental pollutant that produces toxic effects on gametogenesis, pre- and post-implantation embryos, and the placenta. Because the effects of acute Cd intoxication on the placenta are not well understood, we investigated changes in its glycosylated components in Cd treated dams at days 4, 7, 10 and 15 of gestation using lectin histochemistry. CdCl 2 was administered to pregnant rats; control animals received sterile normal saline. Placentas were processed for DBA, Con A, SBA, PNA, UEA-I, RCA-I and WGA lectin histochemistry to evaluate changes in the carbohydrate pattern of the placenta that might modify cell interactions and contribute to embryonic alterations. Lectin binding was analyzed in the yolk sac; trophoblast giant cells; trophoblast I, II and III; spongiotrophoblast cells and endovascular trophoblast cells in the chorioallantoic placenta. Our lectin binding patterns showed that Cd caused alteration of SBA and DBA labeling of trophoblast-derived cells, which suggested increased expressions of α and β GalNAc. Cd also caused decreased UEA-1 binding affinity, which indicated fewer α-L-Fuc residues in placentas of Cd treated dams. The nonreactivity in trophoblast I of the control placentas incubated with Con-A contrasted with the labeling in placentas of experimental dams, which indicated increased expression of terminal α-D-Man, and α-D-Glc residues. We found that Cd altered the reactivity of placenta to several lectins, which indicated modification of the glycotype presented by the fetal component of the placenta. We report that Cd exerts a deleterious effect on the glycosylation pattern of the placenta.</abstract><cop>England</cop><pub>Taylor &amp; Francis</pub><pmid>28166424</pmid><doi>10.1080/10520295.2016.1185668</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1052-0295
ispartof Biotechnic & histochemistry, 2017-01, Vol.92 (1), p.36-45
issn 1052-0295
1473-7760
language eng
recordid cdi_pubmed_primary_28166424
source Taylor and Francis Science and Technology Collection
subjects Animals
cadmium
Cadmium - toxicity
carbohydrate moieties
Female
glycoproteins
Glycosylation
lectin histochemistry
Lectins - chemistry
placenta
Placenta - drug effects
Placenta - metabolism
Pregnancy
rat
Rats
Rats, Wistar
Trophoblasts - drug effects
Trophoblasts - physiology
title Lectin histochemistry for detecting cadmium-induced changes in the glycosylation pattern of rat placenta
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T22%3A27%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Lectin%20histochemistry%20for%20detecting%20cadmium-induced%20changes%20in%20the%20glycosylation%20pattern%20of%20rat%20placenta&rft.jtitle=Biotechnic%20&%20histochemistry&rft.au=D%C3%ADaz,%20MC&rft.date=2017-01-02&rft.volume=92&rft.issue=1&rft.spage=36&rft.epage=45&rft.pages=36-45&rft.issn=1052-0295&rft.eissn=1473-7760&rft_id=info:doi/10.1080/10520295.2016.1185668&rft_dat=%3Cpubmed_infor%3E28166424%3C/pubmed_infor%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c366t-925da53310261195d37b49cd216c441c2498e506c430c7ad239f9554989a67923%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/28166424&rfr_iscdi=true