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Survivin is expressed on CD40 stimulation and interfaces proliferation and apoptosis in B-cell chronic lymphocytic leukemia
In B-cell chronic lymphocytic leukemia (B-CLL), defective apoptosis causes the accumulation of mature CD5+ B cells in lymphoid organs, bone marrow (BM), and peripheral blood (PB). These cells are the progeny of a proliferating pool that feeds the accumulating compartment. The authors sought to deter...
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Published in: | Blood 2001-05, Vol.97 (9), p.2777-2783 |
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description | In B-cell chronic lymphocytic leukemia (B-CLL), defective apoptosis causes the accumulation of mature CD5+ B cells in lymphoid organs, bone marrow (BM), and peripheral blood (PB). These cells are the progeny of a proliferating pool that feeds the accumulating compartment. The authors sought to determine which molecular mechanisms govern the proliferating pool, how they relate to apoptosis, and what the role is of the microenvironment. To begin to resolve these problems, the expression and modulation of the family of inhibitor of apoptosis proteins (IAPs) were investigated, with consideration given to the possibility that physiological stimuli, such as CD40 ligand (CD40L), available to B cells in the microenvironment, might modulate IAP expression. The in vitro data on mononuclear cells from PB or BM of 30 patients demonstrate that B-CLL cells on CD40 stimulation express Survivin and that Survivin is the only IAP whose expression is induced by CD40L. Through immunohistochemistry, in vivo Survivin expression in lymph node (LN) and BM biopsies was evaluated. In reactive LN, Survivin was detected only in highly proliferating germinal center cells. In LN from patients with B-CLL, Survivin was detected only in pseudofollicles. Pseudofollicle Survivin+ cells were actively proliferating and, in contrast to Survivin+ B cells found in normal GC, were Bcl-2+. In B-CLL BM biopsies, CD5+, Survivin+ cells were observed in clusters interspersed with T cells. These findings establish that Survivin controls the B-CLL proliferative pool interfacing apoptosis and that its expression may be modulated by microenvironmental stimuli. |
doi_str_mv | 10.1182/blood.V97.9.2777 |
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In LN from patients with B-CLL, Survivin was detected only in pseudofollicles. Pseudofollicle Survivin+ cells were actively proliferating and, in contrast to Survivin+ B cells found in normal GC, were Bcl-2+. In B-CLL BM biopsies, CD5+, Survivin+ cells were observed in clusters interspersed with T cells. These findings establish that Survivin controls the B-CLL proliferative pool interfacing apoptosis and that its expression may be modulated by microenvironmental stimuli.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.V97.9.2777</identifier><identifier>PMID: 11313271</identifier><language>eng</language><publisher>Washington, DC: Elsevier Inc</publisher><subject>Aged ; Aged, 80 and over ; Apoptosis - immunology ; Biological and medical sciences ; CD40 Antigens - immunology ; Cell Division - immunology ; Female ; Hematologic and hematopoietic diseases ; Humans ; Inhibitor of Apoptosis Proteins ; Leukemia, Lymphocytic, Chronic, B-Cell - immunology ; Leukemia, Lymphocytic, Chronic, B-Cell - metabolism ; Leukemia, Lymphocytic, Chronic, B-Cell - pathology ; Leukemias. Malignant lymphomas. Malignant reticulosis. 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In LN from patients with B-CLL, Survivin was detected only in pseudofollicles. Pseudofollicle Survivin+ cells were actively proliferating and, in contrast to Survivin+ B cells found in normal GC, were Bcl-2+. In B-CLL BM biopsies, CD5+, Survivin+ cells were observed in clusters interspersed with T cells. These findings establish that Survivin controls the B-CLL proliferative pool interfacing apoptosis and that its expression may be modulated by microenvironmental stimuli.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Apoptosis - immunology</subject><subject>Biological and medical sciences</subject><subject>CD40 Antigens - immunology</subject><subject>Cell Division - immunology</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Inhibitor of Apoptosis Proteins</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - immunology</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - metabolism</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - pathology</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microtubule-Associated Proteins</subject><subject>Neoplasm Proteins</subject><subject>Protein Biosynthesis</subject><subject>Proteins - immunology</subject><subject>Survivin</subject><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp1kE1v1DAQhq0K1G4Ld07IB9RblrGdxAk3uv0AqRIHPq6WY49VQxIHO1mx4s_X212pXDh55Hnm1auHkDcM1ow1_H3Xh2DXP1q5btdcSnlCVqziTQHA4QVZAUBdlK1kZ-Q8pZ8ArBS8OiVnjAkmuGQr8vfrErd-60fqE8U_U8SU0NIw0s11CTTNflh6Pfv8oUdL_ThjdNpgolMMvXcYn5d6CtMcUg7KcVeFwb6n5iGG0Rva74bpIZjdvJ9x-YWD16_IS6f7hK-P7wX5fnvzbfOpuP9y93nz8b4wlYC5aJw0RsgSOWt5VzdON9xWWtiqY5yBc7x2bedqWVet1AzzYBrhnBO2dsC5uCCXh9xc-feCaVaDT_t2esSwJCUlyJozmUE4gCaGlCI6NUU_6LhTDNReuHoSrrJw1aq98Hzy9pi9dAPa54Oj4Qy8OwI6Gd27qEfj0z_BpQQGGftwwDCL2HqMKhmPo0HrI5pZ2eD_X-IRGH6gPQ</recordid><startdate>20010501</startdate><enddate>20010501</enddate><creator>Granziero, Luisa</creator><creator>Ghia, Paolo</creator><creator>Circosta, Paola</creator><creator>Gottardi, Daniela</creator><creator>Strola, Giuliana</creator><creator>Geuna, Massimo</creator><creator>Montagna, Licia</creator><creator>Piccoli, Paola</creator><creator>Chilosi, Marco</creator><creator>Caligaris-Cappio, Federico</creator><general>Elsevier Inc</general><general>The Americain Society of Hematology</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><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>20010501</creationdate><title>Survivin is expressed on CD40 stimulation and interfaces proliferation and apoptosis in B-cell chronic lymphocytic leukemia</title><author>Granziero, Luisa ; Ghia, Paolo ; Circosta, Paola ; Gottardi, Daniela ; Strola, Giuliana ; Geuna, Massimo ; Montagna, Licia ; Piccoli, Paola ; Chilosi, Marco ; Caligaris-Cappio, Federico</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c530t-8f7cc374e2192b68fa82d5a3d5b1210ff26f9bf676597a1e676c83fff3d6f0223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Apoptosis - immunology</topic><topic>Biological and medical sciences</topic><topic>CD40 Antigens - immunology</topic><topic>Cell Division - immunology</topic><topic>Female</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Inhibitor of Apoptosis Proteins</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - immunology</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - metabolism</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - pathology</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microtubule-Associated Proteins</topic><topic>Neoplasm Proteins</topic><topic>Protein Biosynthesis</topic><topic>Proteins - immunology</topic><topic>Survivin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Granziero, Luisa</creatorcontrib><creatorcontrib>Ghia, Paolo</creatorcontrib><creatorcontrib>Circosta, Paola</creatorcontrib><creatorcontrib>Gottardi, Daniela</creatorcontrib><creatorcontrib>Strola, Giuliana</creatorcontrib><creatorcontrib>Geuna, Massimo</creatorcontrib><creatorcontrib>Montagna, Licia</creatorcontrib><creatorcontrib>Piccoli, Paola</creatorcontrib><creatorcontrib>Chilosi, Marco</creatorcontrib><creatorcontrib>Caligaris-Cappio, Federico</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><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>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Granziero, Luisa</au><au>Ghia, Paolo</au><au>Circosta, Paola</au><au>Gottardi, Daniela</au><au>Strola, Giuliana</au><au>Geuna, Massimo</au><au>Montagna, Licia</au><au>Piccoli, Paola</au><au>Chilosi, Marco</au><au>Caligaris-Cappio, Federico</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Survivin is expressed on CD40 stimulation and interfaces proliferation and apoptosis in B-cell chronic lymphocytic leukemia</atitle><jtitle>Blood</jtitle><addtitle>Blood</addtitle><date>2001-05-01</date><risdate>2001</risdate><volume>97</volume><issue>9</issue><spage>2777</spage><epage>2783</epage><pages>2777-2783</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>In B-cell chronic lymphocytic leukemia (B-CLL), defective apoptosis causes the accumulation of mature CD5+ B cells in lymphoid organs, bone marrow (BM), and peripheral blood (PB). These cells are the progeny of a proliferating pool that feeds the accumulating compartment. The authors sought to determine which molecular mechanisms govern the proliferating pool, how they relate to apoptosis, and what the role is of the microenvironment. To begin to resolve these problems, the expression and modulation of the family of inhibitor of apoptosis proteins (IAPs) were investigated, with consideration given to the possibility that physiological stimuli, such as CD40 ligand (CD40L), available to B cells in the microenvironment, might modulate IAP expression. The in vitro data on mononuclear cells from PB or BM of 30 patients demonstrate that B-CLL cells on CD40 stimulation express Survivin and that Survivin is the only IAP whose expression is induced by CD40L. Through immunohistochemistry, in vivo Survivin expression in lymph node (LN) and BM biopsies was evaluated. In reactive LN, Survivin was detected only in highly proliferating germinal center cells. In LN from patients with B-CLL, Survivin was detected only in pseudofollicles. Pseudofollicle Survivin+ cells were actively proliferating and, in contrast to Survivin+ B cells found in normal GC, were Bcl-2+. In B-CLL BM biopsies, CD5+, Survivin+ cells were observed in clusters interspersed with T cells. These findings establish that Survivin controls the B-CLL proliferative pool interfacing apoptosis and that its expression may be modulated by microenvironmental stimuli.</abstract><cop>Washington, DC</cop><pub>Elsevier Inc</pub><pmid>11313271</pmid><doi>10.1182/blood.V97.9.2777</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Aged, 80 and over Apoptosis - immunology Biological and medical sciences CD40 Antigens - immunology Cell Division - immunology Female Hematologic and hematopoietic diseases Humans Inhibitor of Apoptosis Proteins Leukemia, Lymphocytic, Chronic, B-Cell - immunology Leukemia, Lymphocytic, Chronic, B-Cell - metabolism Leukemia, Lymphocytic, Chronic, B-Cell - pathology Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Medical sciences Microtubule-Associated Proteins Neoplasm Proteins Protein Biosynthesis Proteins - immunology Survivin |
title | Survivin is expressed on CD40 stimulation and interfaces proliferation and apoptosis in B-cell chronic lymphocytic leukemia |
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