Loading…

Ascitic growth of a spontaneous transplantable T cell lymphoma induces thymic involution. 2. Induction of apoptosis in thymocytes

It has been observed that the progressive ascitic growth of a transplantable T cell lymphoma of spontaneous origin, designated as Dalton's lymphoma (DL), induces inhibition of various immune responses and is associated with an involution of the thymus accompanied by a massive depletion of the c...

Full description

Saved in:
Bibliographic Details
Published in:Tumor biology 2000-11, Vol.21 (6), p.315-327
Main Authors: SHANKER, Anil, MAHENDRA, Sukh, SINGH AJIT SODHI
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 327
container_issue 6
container_start_page 315
container_title Tumor biology
container_volume 21
creator SHANKER, Anil
MAHENDRA, Sukh
SINGH AJIT SODHI
description It has been observed that the progressive ascitic growth of a transplantable T cell lymphoma of spontaneous origin, designated as Dalton's lymphoma (DL), induces inhibition of various immune responses and is associated with an involution of the thymus accompanied by a massive depletion of the cortical region and alteration in the distribution of thymocytes, with a decrease in CD4+CD8+, CD4+CD8- and CD4-CD8+ thymocytes. Morphological evaluation of thymocytes from DL-bearing mice revealed that with the progression of DL, a majority of thymocytes exhibited morphological features characteristic of apoptotic cell death, which included contracted cell bodies, condensed, uniformly circumscribed and densely stained chromatin, and membrane-bound apoptotic bodies containing one or more nuclear fragments. Quantitative and qualitative analysis of the DNA extracted from the thymocytes of DL-bearing mice revealed DNA fragmentation that increased concomitantly with the progression of DL and showed an oligonucleosomal DNA ladder pattern upon agarose gel electrophoresis, a hallmark of apoptotic cell death. Attempts to identify apoptotic factor(s) showed that the serum of DL-bearing mice contained certain soluble factor(s) that augmented the induction of apoptotis in thymocytes in a time- and dose-dependent manner. Although DL cells or their products, such as DL-cell-conditioned medium or DL-cell-free ascitic fluid, could also induce apoptosis of thymocytes in vitro, the magnitude of the same was consistently lower than that induced by the serum of DL-bearing mice. Further, elucidation of the mechanism of apoptosis induction in thymocytes with respect to the involvement of apoptosis-related genes revealed that the death pathway followed an interleukin-1 beta-converting-enzyme-dependent, Fas-mediated apoptotic cascade, with a concomitant increase in the protein products of the bax, bad, p53, fas and fasL genes and cleavage of the 23-kD N-terminal fragment of Bcl-2 that exhibited Bax-like death effector properties.
doi_str_mv 10.1159/000030137
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_72295219</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>677603671</sourcerecordid><originalsourceid>FETCH-LOGICAL-p263t-587e2bf6a65bac4db6e4e28d85bd753436225c1309dfa31860c347cad74721b33</originalsourceid><addsrcrecordid>eNpd0FtLwzAUB_AgipvTB7-ABBHfOpOTpmkfx_AyGPgyn0uapi6jbWqTKnv0m5tdRDAvuf34c85B6JqSKaU8eyBhMUKZOEFjGgOLCEvJaTgTSqIYUjZCF85tCAk4S87RiFJCEi5gjL5nThlvFH7v7ZdfY1thiV1nWy9bbQeHfS9b19UyPBS1xiusdF3jett0a9tIbNpyUDqw9bYJKab9tPXgjW2nGKZ4sfvd3fa5ne28dcYFtfdWbb12l-iskrXTV8d9gt6eHlfzl2j5-ryYz5ZRBwnzEU-FhqJKZMILqeKySHSsIS1TXpSCs5glAFxRRrKykoymCVEsFkqWIhZAC8Ym6P6Q2_X2Y9DO541xu2YOjeYCIONAswBv_8GNHfo21JYDgCAi5ru0myMaikaXedebRvbb_HeyAdwdgXRK1lUYozLuz3HglHD2A7pahyA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>222707453</pqid></control><display><type>article</type><title>Ascitic growth of a spontaneous transplantable T cell lymphoma induces thymic involution. 2. Induction of apoptosis in thymocytes</title><source>Publicly Available Content Database</source><creator>SHANKER, Anil ; MAHENDRA, Sukh ; SINGH AJIT SODHI</creator><creatorcontrib>SHANKER, Anil ; MAHENDRA, Sukh ; SINGH AJIT SODHI</creatorcontrib><description>It has been observed that the progressive ascitic growth of a transplantable T cell lymphoma of spontaneous origin, designated as Dalton's lymphoma (DL), induces inhibition of various immune responses and is associated with an involution of the thymus accompanied by a massive depletion of the cortical region and alteration in the distribution of thymocytes, with a decrease in CD4+CD8+, CD4+CD8- and CD4-CD8+ thymocytes. Morphological evaluation of thymocytes from DL-bearing mice revealed that with the progression of DL, a majority of thymocytes exhibited morphological features characteristic of apoptotic cell death, which included contracted cell bodies, condensed, uniformly circumscribed and densely stained chromatin, and membrane-bound apoptotic bodies containing one or more nuclear fragments. Quantitative and qualitative analysis of the DNA extracted from the thymocytes of DL-bearing mice revealed DNA fragmentation that increased concomitantly with the progression of DL and showed an oligonucleosomal DNA ladder pattern upon agarose gel electrophoresis, a hallmark of apoptotic cell death. Attempts to identify apoptotic factor(s) showed that the serum of DL-bearing mice contained certain soluble factor(s) that augmented the induction of apoptotis in thymocytes in a time- and dose-dependent manner. Although DL cells or their products, such as DL-cell-conditioned medium or DL-cell-free ascitic fluid, could also induce apoptosis of thymocytes in vitro, the magnitude of the same was consistently lower than that induced by the serum of DL-bearing mice. Further, elucidation of the mechanism of apoptosis induction in thymocytes with respect to the involvement of apoptosis-related genes revealed that the death pathway followed an interleukin-1 beta-converting-enzyme-dependent, Fas-mediated apoptotic cascade, with a concomitant increase in the protein products of the bax, bad, p53, fas and fasL genes and cleavage of the 23-kD N-terminal fragment of Bcl-2 that exhibited Bax-like death effector properties.</description><identifier>ISSN: 1010-4283</identifier><identifier>EISSN: 1423-0380</identifier><identifier>DOI: 10.1159/000030137</identifier><identifier>PMID: 11006572</identifier><identifier>CODEN: OBIMD4</identifier><language>eng</language><publisher>Basel: Karger</publisher><subject>Animals ; Antibodies - pharmacology ; Apoptosis - genetics ; Apoptosis - physiology ; Apoptosis Inducing Factor ; Ascites - pathology ; Ascitic Fluid - metabolism ; Biological and medical sciences ; Caspase Inhibitors ; Cell Division - physiology ; Culture Media ; Cysteine Proteinase Inhibitors - pharmacology ; DNA Fragmentation ; Fas Ligand Protein ; Female ; Flavoproteins - blood ; Flavoproteins - metabolism ; Hematologic and hematopoietic diseases ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Lymphoma, T-Cell - blood ; Lymphoma, T-Cell - pathology ; Male ; Medical sciences ; Membrane Glycoproteins - genetics ; Membrane Glycoproteins - immunology ; Membrane Proteins - blood ; Membrane Proteins - metabolism ; Mice ; Mice, Inbred BALB C ; Neoplasm Transplantation ; Nucleosomes - metabolism ; Nucleosomes - pathology ; Oligopeptides - pharmacology ; T-Lymphocytes - immunology ; T-Lymphocytes - pathology ; Thymus Gland - immunology ; Thymus Gland - pathology</subject><ispartof>Tumor biology, 2000-11, Vol.21 (6), p.315-327</ispartof><rights>2000 INIST-CNRS</rights><rights>Copyright 2000 S. Karger AG, Basel.</rights><rights>Copyright (c) 2000 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/222707453?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1525105$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11006572$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SHANKER, Anil</creatorcontrib><creatorcontrib>MAHENDRA, Sukh</creatorcontrib><creatorcontrib>SINGH AJIT SODHI</creatorcontrib><title>Ascitic growth of a spontaneous transplantable T cell lymphoma induces thymic involution. 2. Induction of apoptosis in thymocytes</title><title>Tumor biology</title><addtitle>Tumour Biol</addtitle><description>It has been observed that the progressive ascitic growth of a transplantable T cell lymphoma of spontaneous origin, designated as Dalton's lymphoma (DL), induces inhibition of various immune responses and is associated with an involution of the thymus accompanied by a massive depletion of the cortical region and alteration in the distribution of thymocytes, with a decrease in CD4+CD8+, CD4+CD8- and CD4-CD8+ thymocytes. Morphological evaluation of thymocytes from DL-bearing mice revealed that with the progression of DL, a majority of thymocytes exhibited morphological features characteristic of apoptotic cell death, which included contracted cell bodies, condensed, uniformly circumscribed and densely stained chromatin, and membrane-bound apoptotic bodies containing one or more nuclear fragments. Quantitative and qualitative analysis of the DNA extracted from the thymocytes of DL-bearing mice revealed DNA fragmentation that increased concomitantly with the progression of DL and showed an oligonucleosomal DNA ladder pattern upon agarose gel electrophoresis, a hallmark of apoptotic cell death. Attempts to identify apoptotic factor(s) showed that the serum of DL-bearing mice contained certain soluble factor(s) that augmented the induction of apoptotis in thymocytes in a time- and dose-dependent manner. Although DL cells or their products, such as DL-cell-conditioned medium or DL-cell-free ascitic fluid, could also induce apoptosis of thymocytes in vitro, the magnitude of the same was consistently lower than that induced by the serum of DL-bearing mice. Further, elucidation of the mechanism of apoptosis induction in thymocytes with respect to the involvement of apoptosis-related genes revealed that the death pathway followed an interleukin-1 beta-converting-enzyme-dependent, Fas-mediated apoptotic cascade, with a concomitant increase in the protein products of the bax, bad, p53, fas and fasL genes and cleavage of the 23-kD N-terminal fragment of Bcl-2 that exhibited Bax-like death effector properties.</description><subject>Animals</subject><subject>Antibodies - pharmacology</subject><subject>Apoptosis - genetics</subject><subject>Apoptosis - physiology</subject><subject>Apoptosis Inducing Factor</subject><subject>Ascites - pathology</subject><subject>Ascitic Fluid - metabolism</subject><subject>Biological and medical sciences</subject><subject>Caspase Inhibitors</subject><subject>Cell Division - physiology</subject><subject>Culture Media</subject><subject>Cysteine Proteinase Inhibitors - pharmacology</subject><subject>DNA Fragmentation</subject><subject>Fas Ligand Protein</subject><subject>Female</subject><subject>Flavoproteins - blood</subject><subject>Flavoproteins - metabolism</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Lymphoma, T-Cell - blood</subject><subject>Lymphoma, T-Cell - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins - genetics</subject><subject>Membrane Glycoproteins - immunology</subject><subject>Membrane Proteins - blood</subject><subject>Membrane Proteins - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Neoplasm Transplantation</subject><subject>Nucleosomes - metabolism</subject><subject>Nucleosomes - pathology</subject><subject>Oligopeptides - pharmacology</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - pathology</subject><subject>Thymus Gland - immunology</subject><subject>Thymus Gland - pathology</subject><issn>1010-4283</issn><issn>1423-0380</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpd0FtLwzAUB_AgipvTB7-ABBHfOpOTpmkfx_AyGPgyn0uapi6jbWqTKnv0m5tdRDAvuf34c85B6JqSKaU8eyBhMUKZOEFjGgOLCEvJaTgTSqIYUjZCF85tCAk4S87RiFJCEi5gjL5nThlvFH7v7ZdfY1thiV1nWy9bbQeHfS9b19UyPBS1xiusdF3jett0a9tIbNpyUDqw9bYJKab9tPXgjW2nGKZ4sfvd3fa5ne28dcYFtfdWbb12l-iskrXTV8d9gt6eHlfzl2j5-ryYz5ZRBwnzEU-FhqJKZMILqeKySHSsIS1TXpSCs5glAFxRRrKykoymCVEsFkqWIhZAC8Ym6P6Q2_X2Y9DO541xu2YOjeYCIONAswBv_8GNHfo21JYDgCAi5ru0myMaikaXedebRvbb_HeyAdwdgXRK1lUYozLuz3HglHD2A7pahyA</recordid><startdate>20001101</startdate><enddate>20001101</enddate><creator>SHANKER, Anil</creator><creator>MAHENDRA, Sukh</creator><creator>SINGH AJIT SODHI</creator><general>Karger</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20001101</creationdate><title>Ascitic growth of a spontaneous transplantable T cell lymphoma induces thymic involution. 2. Induction of apoptosis in thymocytes</title><author>SHANKER, Anil ; MAHENDRA, Sukh ; SINGH AJIT SODHI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p263t-587e2bf6a65bac4db6e4e28d85bd753436225c1309dfa31860c347cad74721b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Antibodies - pharmacology</topic><topic>Apoptosis - genetics</topic><topic>Apoptosis - physiology</topic><topic>Apoptosis Inducing Factor</topic><topic>Ascites - pathology</topic><topic>Ascitic Fluid - metabolism</topic><topic>Biological and medical sciences</topic><topic>Caspase Inhibitors</topic><topic>Cell Division - physiology</topic><topic>Culture Media</topic><topic>Cysteine Proteinase Inhibitors - pharmacology</topic><topic>DNA Fragmentation</topic><topic>Fas Ligand Protein</topic><topic>Female</topic><topic>Flavoproteins - blood</topic><topic>Flavoproteins - metabolism</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Lymphoma, T-Cell - blood</topic><topic>Lymphoma, T-Cell - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Membrane Glycoproteins - genetics</topic><topic>Membrane Glycoproteins - immunology</topic><topic>Membrane Proteins - blood</topic><topic>Membrane Proteins - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Neoplasm Transplantation</topic><topic>Nucleosomes - metabolism</topic><topic>Nucleosomes - pathology</topic><topic>Oligopeptides - pharmacology</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes - pathology</topic><topic>Thymus Gland - immunology</topic><topic>Thymus Gland - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SHANKER, Anil</creatorcontrib><creatorcontrib>MAHENDRA, Sukh</creatorcontrib><creatorcontrib>SINGH AJIT SODHI</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest_Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest research library</collection><collection>ProQuest Biological Science Journals</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Tumor biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SHANKER, Anil</au><au>MAHENDRA, Sukh</au><au>SINGH AJIT SODHI</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ascitic growth of a spontaneous transplantable T cell lymphoma induces thymic involution. 2. Induction of apoptosis in thymocytes</atitle><jtitle>Tumor biology</jtitle><addtitle>Tumour Biol</addtitle><date>2000-11-01</date><risdate>2000</risdate><volume>21</volume><issue>6</issue><spage>315</spage><epage>327</epage><pages>315-327</pages><issn>1010-4283</issn><eissn>1423-0380</eissn><coden>OBIMD4</coden><abstract>It has been observed that the progressive ascitic growth of a transplantable T cell lymphoma of spontaneous origin, designated as Dalton's lymphoma (DL), induces inhibition of various immune responses and is associated with an involution of the thymus accompanied by a massive depletion of the cortical region and alteration in the distribution of thymocytes, with a decrease in CD4+CD8+, CD4+CD8- and CD4-CD8+ thymocytes. Morphological evaluation of thymocytes from DL-bearing mice revealed that with the progression of DL, a majority of thymocytes exhibited morphological features characteristic of apoptotic cell death, which included contracted cell bodies, condensed, uniformly circumscribed and densely stained chromatin, and membrane-bound apoptotic bodies containing one or more nuclear fragments. Quantitative and qualitative analysis of the DNA extracted from the thymocytes of DL-bearing mice revealed DNA fragmentation that increased concomitantly with the progression of DL and showed an oligonucleosomal DNA ladder pattern upon agarose gel electrophoresis, a hallmark of apoptotic cell death. Attempts to identify apoptotic factor(s) showed that the serum of DL-bearing mice contained certain soluble factor(s) that augmented the induction of apoptotis in thymocytes in a time- and dose-dependent manner. Although DL cells or their products, such as DL-cell-conditioned medium or DL-cell-free ascitic fluid, could also induce apoptosis of thymocytes in vitro, the magnitude of the same was consistently lower than that induced by the serum of DL-bearing mice. Further, elucidation of the mechanism of apoptosis induction in thymocytes with respect to the involvement of apoptosis-related genes revealed that the death pathway followed an interleukin-1 beta-converting-enzyme-dependent, Fas-mediated apoptotic cascade, with a concomitant increase in the protein products of the bax, bad, p53, fas and fasL genes and cleavage of the 23-kD N-terminal fragment of Bcl-2 that exhibited Bax-like death effector properties.</abstract><cop>Basel</cop><pub>Karger</pub><pmid>11006572</pmid><doi>10.1159/000030137</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1010-4283
ispartof Tumor biology, 2000-11, Vol.21 (6), p.315-327
issn 1010-4283
1423-0380
language eng
recordid cdi_proquest_miscellaneous_72295219
source Publicly Available Content Database
subjects Animals
Antibodies - pharmacology
Apoptosis - genetics
Apoptosis - physiology
Apoptosis Inducing Factor
Ascites - pathology
Ascitic Fluid - metabolism
Biological and medical sciences
Caspase Inhibitors
Cell Division - physiology
Culture Media
Cysteine Proteinase Inhibitors - pharmacology
DNA Fragmentation
Fas Ligand Protein
Female
Flavoproteins - blood
Flavoproteins - metabolism
Hematologic and hematopoietic diseases
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
Lymphoma, T-Cell - blood
Lymphoma, T-Cell - pathology
Male
Medical sciences
Membrane Glycoproteins - genetics
Membrane Glycoproteins - immunology
Membrane Proteins - blood
Membrane Proteins - metabolism
Mice
Mice, Inbred BALB C
Neoplasm Transplantation
Nucleosomes - metabolism
Nucleosomes - pathology
Oligopeptides - pharmacology
T-Lymphocytes - immunology
T-Lymphocytes - pathology
Thymus Gland - immunology
Thymus Gland - pathology
title Ascitic growth of a spontaneous transplantable T cell lymphoma induces thymic involution. 2. Induction of apoptosis in thymocytes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T06%3A20%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ascitic%20growth%20of%20a%20spontaneous%20transplantable%20T%20cell%20lymphoma%20induces%20thymic%20involution.%202.%20Induction%20of%20apoptosis%20in%20thymocytes&rft.jtitle=Tumor%20biology&rft.au=SHANKER,%20Anil&rft.date=2000-11-01&rft.volume=21&rft.issue=6&rft.spage=315&rft.epage=327&rft.pages=315-327&rft.issn=1010-4283&rft.eissn=1423-0380&rft.coden=OBIMD4&rft_id=info:doi/10.1159/000030137&rft_dat=%3Cproquest_pubme%3E677603671%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-p263t-587e2bf6a65bac4db6e4e28d85bd753436225c1309dfa31860c347cad74721b33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=222707453&rft_id=info:pmid/11006572&rfr_iscdi=true