Production of stress-inducible form of heat-shock protein 70 in mouse peritoneal adherent cells afterin Vivo infection byFrancisella tularensis
Heat-shock proteins (hsp) are ubiquitously produced molecules which participate in the protection of cells from environmental perturbation. Moreover, the members of the heat-shock protein 60 (hsp60) and 70 (hsp70) families play an important role in pathogen-host interactions. We studiedin vivo produ...
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Veröffentlicht in: | Folia microbiologica 1999-06, Vol.44 (3), p.306-310 |
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description | Heat-shock proteins (hsp) are ubiquitously produced molecules which participate in the protection of cells from environmental perturbation. Moreover, the members of the heat-shock protein 60 (hsp60) and 70 (hsp70) families play an important role in pathogen-host interactions. We studiedin vivo production of the 70-kDa heat-shock proteins in the extract of peritoneal exudate cells (PEC) from mice injected intraperitoneally with an attenuated vaccine strain (LVS) ofFrancisella tularensis. We found a differential production of a highly stress-inducible member of the hsp70 family, designated hsp72, in three inbred strains of mice exhibiting either resistance or susceptibility toF. tularensis LVS infection. Whereas in tularemia-resistant mice hsp72 was even expressed in PEC without injection of bacteria and its production further increased on day 3 and slowly declined on days 5 and 7 after injection, in susceptible mice hsp72 production was highly inducble and restricted only to day 3 afterin vivo infection. Further analysis of hsp72 expression revealed intracellular hsp72 accumulation and its preferential production by peritoneal adherent cells. |
doi_str_mv | 10.1007/BF02818552 |
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Moreover, the members of the heat-shock protein 60 (hsp60) and 70 (hsp70) families play an important role in pathogen-host interactions. We studiedin vivo production of the 70-kDa heat-shock proteins in the extract of peritoneal exudate cells (PEC) from mice injected intraperitoneally with an attenuated vaccine strain (LVS) ofFrancisella tularensis. We found a differential production of a highly stress-inducible member of the hsp70 family, designated hsp72, in three inbred strains of mice exhibiting either resistance or susceptibility toF. tularensis LVS infection. Whereas in tularemia-resistant mice hsp72 was even expressed in PEC without injection of bacteria and its production further increased on day 3 and slowly declined on days 5 and 7 after injection, in susceptible mice hsp72 production was highly inducble and restricted only to day 3 afterin vivo infection. Further analysis of hsp72 expression revealed intracellular hsp72 accumulation and its preferential production by peritoneal adherent cells.</description><identifier>ISSN: 0015-5632</identifier><identifier>EISSN: 1874-9356</identifier><identifier>DOI: 10.1007/BF02818552</identifier><language>eng</language><publisher>Dordrecht: Springer Nature B.V</publisher><subject>Adherent cells ; Exudation ; Heat ; Heat shock proteins ; Hsp60 protein ; Hsp70 protein ; Hsp72 protein ; Inbreeding ; Injection ; Medical research ; Peritoneal exudate cells ; Peritoneum ; Perturbation ; Proteins ; Rodents ; Shock ; Tularemia</subject><ispartof>Folia microbiologica, 1999-06, Vol.44 (3), p.306-310</ispartof><rights>Institute of Microbiology, Academy of Sciences of the Czech Republic 1999.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1357-d0af5f444ddab7ae4cc6aed47969ffb4086acb8eb2305307c453a490bc90293d3</citedby><cites>FETCH-LOGICAL-c1357-d0af5f444ddab7ae4cc6aed47969ffb4086acb8eb2305307c453a490bc90293d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Stulík, J.</creatorcontrib><creatorcontrib>Hernychová, L.</creatorcontrib><creatorcontrib>Macela, A.</creatorcontrib><creatorcontrib>Kročová, Z.</creatorcontrib><creatorcontrib>Kroča, M.</creatorcontrib><title>Production of stress-inducible form of heat-shock protein 70 in mouse peritoneal adherent cells afterin Vivo infection byFrancisella tularensis</title><title>Folia microbiologica</title><description>Heat-shock proteins (hsp) are ubiquitously produced molecules which participate in the protection of cells from environmental perturbation. Moreover, the members of the heat-shock protein 60 (hsp60) and 70 (hsp70) families play an important role in pathogen-host interactions. We studiedin vivo production of the 70-kDa heat-shock proteins in the extract of peritoneal exudate cells (PEC) from mice injected intraperitoneally with an attenuated vaccine strain (LVS) ofFrancisella tularensis. We found a differential production of a highly stress-inducible member of the hsp70 family, designated hsp72, in three inbred strains of mice exhibiting either resistance or susceptibility toF. tularensis LVS infection. Whereas in tularemia-resistant mice hsp72 was even expressed in PEC without injection of bacteria and its production further increased on day 3 and slowly declined on days 5 and 7 after injection, in susceptible mice hsp72 production was highly inducble and restricted only to day 3 afterin vivo infection. Further analysis of hsp72 expression revealed intracellular hsp72 accumulation and its preferential production by peritoneal adherent cells.</description><subject>Adherent cells</subject><subject>Exudation</subject><subject>Heat</subject><subject>Heat shock proteins</subject><subject>Hsp60 protein</subject><subject>Hsp70 protein</subject><subject>Hsp72 protein</subject><subject>Inbreeding</subject><subject>Injection</subject><subject>Medical research</subject><subject>Peritoneal exudate cells</subject><subject>Peritoneum</subject><subject>Perturbation</subject><subject>Proteins</subject><subject>Rodents</subject><subject>Shock</subject><subject>Tularemia</subject><issn>0015-5632</issn><issn>1874-9356</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkU1r3DAQhkVJoJu0l_4CkUuh4HT0ZdnHNmTTwEJ7SHo1sjxilXqljSQH8ivyl6NlC4FcZmDeZz5ehpAvDC4ZgP7-cw28Y51S_ANZsU7LpheqPSErAKYa1Qr-kZzl_ADQghR8RV7-pDgttvgYaHQ0l4Q5Nz7Umh9npC6m3UHYoilN3kb7j-5TLOgD1UBr3MUlI91j8iUGNDM10xYThkItznOmxpWqBfrXP8XKOzzuGp_XyQTrc4UMLctsak_2-RM5dWbO-Pl_Pif36-u7q1_N5vfN7dWPTWOZULqZwDjlpJTTZEZtUFrbGpyk7tveuVFC1xo7djhyAUqAtlIJI3sYbQ-8F5M4J1-Pc6ubxwVzGXY-Hy42AaujoQPNteBMV_LiHfkQlxTqcYNWsmecMV6hb0fIpphzQjfsk9-Z9DwwGA6fGd4-I14BzkWDAA</recordid><startdate>19990601</startdate><enddate>19990601</enddate><creator>Stulík, J.</creator><creator>Hernychová, L.</creator><creator>Macela, A.</creator><creator>Kročová, Z.</creator><creator>Kroča, M.</creator><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>19990601</creationdate><title>Production of stress-inducible form of heat-shock protein 70 in mouse peritoneal adherent cells afterin Vivo infection byFrancisella tularensis</title><author>Stulík, J. ; 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Moreover, the members of the heat-shock protein 60 (hsp60) and 70 (hsp70) families play an important role in pathogen-host interactions. We studiedin vivo production of the 70-kDa heat-shock proteins in the extract of peritoneal exudate cells (PEC) from mice injected intraperitoneally with an attenuated vaccine strain (LVS) ofFrancisella tularensis. We found a differential production of a highly stress-inducible member of the hsp70 family, designated hsp72, in three inbred strains of mice exhibiting either resistance or susceptibility toF. tularensis LVS infection. Whereas in tularemia-resistant mice hsp72 was even expressed in PEC without injection of bacteria and its production further increased on day 3 and slowly declined on days 5 and 7 after injection, in susceptible mice hsp72 production was highly inducble and restricted only to day 3 afterin vivo infection. Further analysis of hsp72 expression revealed intracellular hsp72 accumulation and its preferential production by peritoneal adherent cells.</abstract><cop>Dordrecht</cop><pub>Springer Nature B.V</pub><doi>10.1007/BF02818552</doi><tpages>5</tpages></addata></record> |
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subjects | Adherent cells Exudation Heat Heat shock proteins Hsp60 protein Hsp70 protein Hsp72 protein Inbreeding Injection Medical research Peritoneal exudate cells Peritoneum Perturbation Proteins Rodents Shock Tularemia |
title | Production of stress-inducible form of heat-shock protein 70 in mouse peritoneal adherent cells afterin Vivo infection byFrancisella tularensis |
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