B-cell lymphopoiesis is regulated by cathepsin L.

Cathepsin L (CTSL) is a ubiquitously expressed lysosomal cysteine peptidase with diverse and highly specific functions. The involvement of CTSL in thymic CD4+ T-cell positive selection has been well documented. Using CTSL(nkt/nkt) mice that lack CTSL activity, we have previously demonstrated that th...

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Main Authors: Maria Noel Badano, Gabriela Lorena Camicia, Gabriela Lombardi, Andrea Maglioco, Gabriel Cabrera, Hector Costa, Roberto Pablo Meiss, Isabel Piazzon, Irene Nepomnaschy
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3621861?pdf=render
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author Maria Noel Badano
Gabriela Lorena Camicia
Gabriela Lombardi
Andrea Maglioco
Gabriel Cabrera
Hector Costa
Roberto Pablo Meiss
Isabel Piazzon
Irene Nepomnaschy
author_facet Maria Noel Badano
Gabriela Lorena Camicia
Gabriela Lombardi
Andrea Maglioco
Gabriel Cabrera
Hector Costa
Roberto Pablo Meiss
Isabel Piazzon
Irene Nepomnaschy
author_sort Maria Noel Badano
collection DOAJ
description Cathepsin L (CTSL) is a ubiquitously expressed lysosomal cysteine peptidase with diverse and highly specific functions. The involvement of CTSL in thymic CD4+ T-cell positive selection has been well documented. Using CTSL(nkt/nkt) mice that lack CTSL activity, we have previously demonstrated that the absence of CTSL activity affects the homeostasis of the T-cell pool by decreasing CD4+ cell thymic production and increasing CD8+ thymocyte production. Herein we investigated the influence of CTSL activity on the homeostasis of peripheral B-cell populations and bone marrow (BM) B-cell maturation. B-cell numbers were increased in lymph nodes (LN), spleen and blood from CTSL (nkt/nkt) mice. Increases in splenic B-cell numbers were restricted to transitional T1 and T2 cells and to the marginal zone (MZ) cell subpopulation. No alterations in the proliferative or apoptosis levels were detected in peripheral B-cell populations from CTSL (nkt/nkt) mice. In the BM, the percentage and the absolute number of pre-pro-B, pro-B, pre-B, immature and mature B cells were not altered. However, in vitro and in vivo experiments showed that BM B-cell production was markedly increased in CTSL (nkt/nkt) mice. Besides, BM B-cell emigration to the spleen was increased in CTSL (nkt/nkt) mice. Colony-forming unit pre-B (CFU pre-B) assays in the presence of BM stromal cells (SC) and reciprocal BM chimeras revealed that both BM B-cell precursors and SC would contribute to sustain the increased B-cell hematopoiesis in CTSL (nkt/nkt) mice. Overall, our data clearly demonstrate that CTSL negatively regulates BM B-cell production and output therefore influencing the homeostasis of peripheral B cells.
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spelling doaj.art-fb460282bf724fadacab445676e55e672022-12-22T02:40:30ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6134710.1371/journal.pone.0061347B-cell lymphopoiesis is regulated by cathepsin L.Maria Noel BadanoGabriela Lorena CamiciaGabriela LombardiAndrea MagliocoGabriel CabreraHector CostaRoberto Pablo MeissIsabel PiazzonIrene NepomnaschyCathepsin L (CTSL) is a ubiquitously expressed lysosomal cysteine peptidase with diverse and highly specific functions. The involvement of CTSL in thymic CD4+ T-cell positive selection has been well documented. Using CTSL(nkt/nkt) mice that lack CTSL activity, we have previously demonstrated that the absence of CTSL activity affects the homeostasis of the T-cell pool by decreasing CD4+ cell thymic production and increasing CD8+ thymocyte production. Herein we investigated the influence of CTSL activity on the homeostasis of peripheral B-cell populations and bone marrow (BM) B-cell maturation. B-cell numbers were increased in lymph nodes (LN), spleen and blood from CTSL (nkt/nkt) mice. Increases in splenic B-cell numbers were restricted to transitional T1 and T2 cells and to the marginal zone (MZ) cell subpopulation. No alterations in the proliferative or apoptosis levels were detected in peripheral B-cell populations from CTSL (nkt/nkt) mice. In the BM, the percentage and the absolute number of pre-pro-B, pro-B, pre-B, immature and mature B cells were not altered. However, in vitro and in vivo experiments showed that BM B-cell production was markedly increased in CTSL (nkt/nkt) mice. Besides, BM B-cell emigration to the spleen was increased in CTSL (nkt/nkt) mice. Colony-forming unit pre-B (CFU pre-B) assays in the presence of BM stromal cells (SC) and reciprocal BM chimeras revealed that both BM B-cell precursors and SC would contribute to sustain the increased B-cell hematopoiesis in CTSL (nkt/nkt) mice. Overall, our data clearly demonstrate that CTSL negatively regulates BM B-cell production and output therefore influencing the homeostasis of peripheral B cells.http://europepmc.org/articles/PMC3621861?pdf=render
spellingShingle Maria Noel Badano
Gabriela Lorena Camicia
Gabriela Lombardi
Andrea Maglioco
Gabriel Cabrera
Hector Costa
Roberto Pablo Meiss
Isabel Piazzon
Irene Nepomnaschy
B-cell lymphopoiesis is regulated by cathepsin L.
PLoS ONE
title B-cell lymphopoiesis is regulated by cathepsin L.
title_full B-cell lymphopoiesis is regulated by cathepsin L.
title_fullStr B-cell lymphopoiesis is regulated by cathepsin L.
title_full_unstemmed B-cell lymphopoiesis is regulated by cathepsin L.
title_short B-cell lymphopoiesis is regulated by cathepsin L.
title_sort b cell lymphopoiesis is regulated by cathepsin l
url http://europepmc.org/articles/PMC3621861?pdf=render
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