NAD + loading of mammalian cells by electrotransfection leads to increased poly(ADP-ribosyl)ation capacity
Many cellular enzymes use NAD + as coenzyme or substrate, depending on the nature of the enzymatic reaction. Under certain conditions the cellular NAD + concentration may become rate-limiting for such enzymes. For instance, when eucaryotic cells are exposed to high concentrations of DNA-damaging age...
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Veröffentlicht in: | Biochimie 1997-04, Vol.79 (4), p.175-178 |
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creator | Küpper, J.H. Wolf, I. Bürkle, A. |
description | Many cellular enzymes use NAD
+ as coenzyme or substrate, depending on the nature of the enzymatic reaction. Under certain conditions the cellular NAD
+ concentration may become rate-limiting for such enzymes. For instance, when eucaryotic cells are exposed to high concentrations of DNA-damaging agents, the resulting DNA strand breaks may stimulate the nuclear enzyme poly(ADP-ribose) polymerase (PARP) to such an extent that the cellular pool of NAD
+, which is the substrate for this enzyme, is severely depleted, possibly leading to acute cell death. Here we show that NAD
+ concentrations in CV-1 monkey and CO60 hamster cells can be raised 3- to 4-fold by electrotransfection of NAD
+. This additional NAD
+ is indeed available for PARP to synthesize higher-than-normal amounts of p poly(ADP-ribose) after treatment with the alkylating agent
N-methyl-
N′-nitro-
N-nitrosoguanidine. NAD
+ loading of cells by electrotransfection may be useful also for the study of other cellular reactions in which NAD
+ is involved. |
doi_str_mv | 10.1016/S0300-9084(97)83503-1 |
format | Article |
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+ as coenzyme or substrate, depending on the nature of the enzymatic reaction. Under certain conditions the cellular NAD
+ concentration may become rate-limiting for such enzymes. For instance, when eucaryotic cells are exposed to high concentrations of DNA-damaging agents, the resulting DNA strand breaks may stimulate the nuclear enzyme poly(ADP-ribose) polymerase (PARP) to such an extent that the cellular pool of NAD
+, which is the substrate for this enzyme, is severely depleted, possibly leading to acute cell death. Here we show that NAD
+ concentrations in CV-1 monkey and CO60 hamster cells can be raised 3- to 4-fold by electrotransfection of NAD
+. This additional NAD
+ is indeed available for PARP to synthesize higher-than-normal amounts of p poly(ADP-ribose) after treatment with the alkylating agent
N-methyl-
N′-nitro-
N-nitrosoguanidine. NAD
+ loading of cells by electrotransfection may be useful also for the study of other cellular reactions in which NAD
+ is involved.</description><identifier>ISSN: 0300-9084</identifier><identifier>EISSN: 1638-6183</identifier><identifier>DOI: 10.1016/S0300-9084(97)83503-1</identifier><identifier>PMID: 9242981</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Animals ; Cell Line ; Cercopithecus aethiops ; Cricetinae ; DNA Adducts ; DNA damage ; Electroporation ; Fluorescent Antibody Technique ; genotoxic stress ; immunofluorescence ; Methylnitronitrosoguanidine - pharmacology ; NAD - metabolism ; poly(ADP-ribose) polymerase ; Poly(ADP-ribose) Polymerases - biosynthesis</subject><ispartof>Biochimie, 1997-04, Vol.79 (4), p.175-178</ispartof><rights>1997</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c308t-507d0b9f3e84dfd49ea550751fe3691afbae68ecca9e4bde3128970c85d933083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0300-9084(97)83503-1$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9242981$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Küpper, J.H.</creatorcontrib><creatorcontrib>Wolf, I.</creatorcontrib><creatorcontrib>Bürkle, A.</creatorcontrib><title>NAD + loading of mammalian cells by electrotransfection leads to increased poly(ADP-ribosyl)ation capacity</title><title>Biochimie</title><addtitle>Biochimie</addtitle><description>Many cellular enzymes use NAD
+ as coenzyme or substrate, depending on the nature of the enzymatic reaction. Under certain conditions the cellular NAD
+ concentration may become rate-limiting for such enzymes. For instance, when eucaryotic cells are exposed to high concentrations of DNA-damaging agents, the resulting DNA strand breaks may stimulate the nuclear enzyme poly(ADP-ribose) polymerase (PARP) to such an extent that the cellular pool of NAD
+, which is the substrate for this enzyme, is severely depleted, possibly leading to acute cell death. Here we show that NAD
+ concentrations in CV-1 monkey and CO60 hamster cells can be raised 3- to 4-fold by electrotransfection of NAD
+. This additional NAD
+ is indeed available for PARP to synthesize higher-than-normal amounts of p poly(ADP-ribose) after treatment with the alkylating agent
N-methyl-
N′-nitro-
N-nitrosoguanidine. NAD
+ loading of cells by electrotransfection may be useful also for the study of other cellular reactions in which NAD
+ is involved.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Cercopithecus aethiops</subject><subject>Cricetinae</subject><subject>DNA Adducts</subject><subject>DNA damage</subject><subject>Electroporation</subject><subject>Fluorescent Antibody Technique</subject><subject>genotoxic stress</subject><subject>immunofluorescence</subject><subject>Methylnitronitrosoguanidine - pharmacology</subject><subject>NAD - metabolism</subject><subject>poly(ADP-ribose) polymerase</subject><subject>Poly(ADP-ribose) Polymerases - biosynthesis</subject><issn>0300-9084</issn><issn>1638-6183</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkFtr3DAQhUVoSLbb_IQFPYWE4ESyfJGeyrKbtoGQFNo8i7E0DgqytZW8Af_7eC_ktU8zzJwzh_kIWXB2yxmv7v4wwVimmCyuVH0tRclExk_IjFdCZhWX4guZfUrOydeU3hhjJcvVGTlTeZEryWfk7Wm5pjfUB7Cuf6WhpR10HXgHPTXofaLNSNGjGWIYIvSpnVoXeuoRbKJDoK43ESGhpZvgx6vl-ncWXRPS6K9hrzSwAeOG8Rs5bcEnvDjWOXn5cf939St7fP75sFo-ZkYwOWQlqy1rVCtQFra1hUIop1nJWxSV4tA2gJVEY0Bh0VgUPJeqZkaWVonpgpiTy8PdTQz_tpgG3bm0-wV6DNuka8XrnJfFJCwPQhNDShFbvYmugzhqzvSOsd4z1juAWtV6z1jzybc4BmybDu2n6wh12n8_7HH68t1h1Mk47A1aFyd62gb3n4QPaCCMfg</recordid><startdate>19970401</startdate><enddate>19970401</enddate><creator>Küpper, J.H.</creator><creator>Wolf, I.</creator><creator>Bürkle, A.</creator><general>Elsevier Masson SAS</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><scope>7X8</scope></search><sort><creationdate>19970401</creationdate><title>NAD + loading of mammalian cells by electrotransfection leads to increased poly(ADP-ribosyl)ation capacity</title><author>Küpper, J.H. ; Wolf, I. ; Bürkle, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c308t-507d0b9f3e84dfd49ea550751fe3691afbae68ecca9e4bde3128970c85d933083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Cercopithecus aethiops</topic><topic>Cricetinae</topic><topic>DNA Adducts</topic><topic>DNA damage</topic><topic>Electroporation</topic><topic>Fluorescent Antibody Technique</topic><topic>genotoxic stress</topic><topic>immunofluorescence</topic><topic>Methylnitronitrosoguanidine - pharmacology</topic><topic>NAD - metabolism</topic><topic>poly(ADP-ribose) polymerase</topic><topic>Poly(ADP-ribose) Polymerases - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Küpper, J.H.</creatorcontrib><creatorcontrib>Wolf, I.</creatorcontrib><creatorcontrib>Bürkle, A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochimie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Küpper, J.H.</au><au>Wolf, I.</au><au>Bürkle, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NAD + loading of mammalian cells by electrotransfection leads to increased poly(ADP-ribosyl)ation capacity</atitle><jtitle>Biochimie</jtitle><addtitle>Biochimie</addtitle><date>1997-04-01</date><risdate>1997</risdate><volume>79</volume><issue>4</issue><spage>175</spage><epage>178</epage><pages>175-178</pages><issn>0300-9084</issn><eissn>1638-6183</eissn><abstract>Many cellular enzymes use NAD
+ as coenzyme or substrate, depending on the nature of the enzymatic reaction. Under certain conditions the cellular NAD
+ concentration may become rate-limiting for such enzymes. For instance, when eucaryotic cells are exposed to high concentrations of DNA-damaging agents, the resulting DNA strand breaks may stimulate the nuclear enzyme poly(ADP-ribose) polymerase (PARP) to such an extent that the cellular pool of NAD
+, which is the substrate for this enzyme, is severely depleted, possibly leading to acute cell death. Here we show that NAD
+ concentrations in CV-1 monkey and CO60 hamster cells can be raised 3- to 4-fold by electrotransfection of NAD
+. This additional NAD
+ is indeed available for PARP to synthesize higher-than-normal amounts of p poly(ADP-ribose) after treatment with the alkylating agent
N-methyl-
N′-nitro-
N-nitrosoguanidine. NAD
+ loading of cells by electrotransfection may be useful also for the study of other cellular reactions in which NAD
+ is involved.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>9242981</pmid><doi>10.1016/S0300-9084(97)83503-1</doi><tpages>4</tpages></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Animals Cell Line Cercopithecus aethiops Cricetinae DNA Adducts DNA damage Electroporation Fluorescent Antibody Technique genotoxic stress immunofluorescence Methylnitronitrosoguanidine - pharmacology NAD - metabolism poly(ADP-ribose) polymerase Poly(ADP-ribose) Polymerases - biosynthesis |
title | NAD + loading of mammalian cells by electrotransfection leads to increased poly(ADP-ribosyl)ation capacity |
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