A prospective study of bone marrow hematopoietic and mesenchymal stem cells in type 1 Gaucher disease patients
Gaucher disease (GD) is an autosomal recessive disorder characterized by lysosomal glucocerebrosidase (GBA) deficiency leading to hematological and skeletal manifestations. Mechanisms underlying these symptoms have not yet been elucidated. In vivo, bone marrow (BM) mesenchymal stem cells (MSCs) have...
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creator | Lecourt, Séverine Mouly, Enguerran Freida, Delphine Cras, Audrey Ceccaldi, Raphaël Heraoui, Djazia Chomienne, Christine Marolleau, Jean-Pierre Arnulf, Bertrand Porcher, Raphael Caillaud, Catherine Vanneaux, Valérie Belmatoug, Nadia Larghero, Jérôme |
description | Gaucher disease (GD) is an autosomal recessive disorder characterized by lysosomal glucocerebrosidase (GBA) deficiency leading to hematological and skeletal manifestations. Mechanisms underlying these symptoms have not yet been elucidated. In vivo, bone marrow (BM) mesenchymal stem cells (MSCs) have important role in the regulation of bone mass and in the support of hematopoiesis, thus representing potential candidate that could contribute to the disease. GBA deficiency may also directly impair hematopoietic stem/progenitors cells (HSPCs) intrinsic function and induce hematological defect. In order to evaluate the role of BM stem cells in GD pathophysiology, we prospectively analyzed BM-MSCs and HSPCs properties in a series of 10 patients with type 1 GD. GBA activity was decreased in all tested cell subtypes. GD-MSCs had an impaired growth potential, morphological and cell cycle abnormalities, decreased capacities to differentiate into osteoblasts. Moreover, GD-MSCs secreted soluble factors that stimulated osteoclasts resorbing activities. In vitro and in vivo primitive and mature hematopoiesis were similar between patients and controls. However, GD-MSCs had a lower hematopoietic supportive capacity than those from healthy donors. These data suggest that BM microenvironment is altered in GD and that MSCs are key components of the manifestations observed in GD. |
doi_str_mv | 10.1371/journal.pone.0069293 |
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Mechanisms underlying these symptoms have not yet been elucidated. In vivo, bone marrow (BM) mesenchymal stem cells (MSCs) have important role in the regulation of bone mass and in the support of hematopoiesis, thus representing potential candidate that could contribute to the disease. GBA deficiency may also directly impair hematopoietic stem/progenitors cells (HSPCs) intrinsic function and induce hematological defect. In order to evaluate the role of BM stem cells in GD pathophysiology, we prospectively analyzed BM-MSCs and HSPCs properties in a series of 10 patients with type 1 GD. GBA activity was decreased in all tested cell subtypes. GD-MSCs had an impaired growth potential, morphological and cell cycle abnormalities, decreased capacities to differentiate into osteoblasts. Moreover, GD-MSCs secreted soluble factors that stimulated osteoclasts resorbing activities. In vitro and in vivo primitive and mature hematopoiesis were similar between patients and controls. However, GD-MSCs had a lower hematopoietic supportive capacity than those from healthy donors. These data suggest that BM microenvironment is altered in GD and that MSCs are key components of the manifestations observed in GD.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0069293</identifier><identifier>PMID: 23935976</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Abnormalities ; Adult ; Aged ; Analysis ; Animals ; Biocompatibility ; Biology ; Biomedical materials ; Bone density ; Bone marrow ; Bone Marrow Cells - enzymology ; Bone Marrow Cells - pathology ; Bone mass ; Case-Control Studies ; Cell cycle ; Cell Differentiation ; Cell Proliferation ; Cellular Microenvironment ; Consent ; Cytokines ; Defects ; Enzymes ; Female ; Gaucher Disease - enzymology ; Gaucher Disease - pathology ; Gaucher's disease ; Glucosylceramidase ; Glucosylceramidase - deficiency ; Hematology ; Hematopoiesis ; Hematopoietic stem cells ; Hematopoietic Stem Cells - enzymology ; Hematopoietic Stem Cells - pathology ; Hereditary diseases ; Humans ; Life Sciences ; Male ; Medical research ; Medicine ; Mesenchymal stem cells ; Mesenchymal Stromal Cells - enzymology ; Mesenchymal Stromal Cells - pathology ; Mesenchyme ; Mice ; Middle Aged ; Multiple myeloma ; Osteoblasts ; Osteoblasts - pathology ; Osteoclasts ; Osteoclasts - pathology ; Patients ; Prospective Studies ; Rodents ; Stem cells</subject><ispartof>PloS one, 2013-07, Vol.8 (7), p.e69293-e69293</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Lecourt et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2013 Lecourt et al 2013 Lecourt et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c726t-3c2400beb76550db765ea5e8cd979c23676ecb9046134f4cd623f7b78b4935c43</citedby><cites>FETCH-LOGICAL-c726t-3c2400beb76550db765ea5e8cd979c23676ecb9046134f4cd623f7b78b4935c43</cites><orcidid>0000-0003-2086-7448</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3723887/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3723887/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2926,23865,27923,27924,53790,53792,79371,79372</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23935976$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04717981$$DView record in HAL$$Hfree_for_read</backlink></links><search><contributor>Dardis, Andrea</contributor><creatorcontrib>Lecourt, Séverine</creatorcontrib><creatorcontrib>Mouly, Enguerran</creatorcontrib><creatorcontrib>Freida, Delphine</creatorcontrib><creatorcontrib>Cras, Audrey</creatorcontrib><creatorcontrib>Ceccaldi, Raphaël</creatorcontrib><creatorcontrib>Heraoui, Djazia</creatorcontrib><creatorcontrib>Chomienne, Christine</creatorcontrib><creatorcontrib>Marolleau, Jean-Pierre</creatorcontrib><creatorcontrib>Arnulf, Bertrand</creatorcontrib><creatorcontrib>Porcher, Raphael</creatorcontrib><creatorcontrib>Caillaud, Catherine</creatorcontrib><creatorcontrib>Vanneaux, Valérie</creatorcontrib><creatorcontrib>Belmatoug, Nadia</creatorcontrib><creatorcontrib>Larghero, Jérôme</creatorcontrib><title>A prospective study of bone marrow hematopoietic and mesenchymal stem cells in type 1 Gaucher disease patients</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Gaucher disease (GD) is an autosomal recessive disorder characterized by lysosomal glucocerebrosidase (GBA) deficiency leading to hematological and skeletal manifestations. Mechanisms underlying these symptoms have not yet been elucidated. In vivo, bone marrow (BM) mesenchymal stem cells (MSCs) have important role in the regulation of bone mass and in the support of hematopoiesis, thus representing potential candidate that could contribute to the disease. GBA deficiency may also directly impair hematopoietic stem/progenitors cells (HSPCs) intrinsic function and induce hematological defect. In order to evaluate the role of BM stem cells in GD pathophysiology, we prospectively analyzed BM-MSCs and HSPCs properties in a series of 10 patients with type 1 GD. GBA activity was decreased in all tested cell subtypes. GD-MSCs had an impaired growth potential, morphological and cell cycle abnormalities, decreased capacities to differentiate into osteoblasts. Moreover, GD-MSCs secreted soluble factors that stimulated osteoclasts resorbing activities. In vitro and in vivo primitive and mature hematopoiesis were similar between patients and controls. However, GD-MSCs had a lower hematopoietic supportive capacity than those from healthy donors. These data suggest that BM microenvironment is altered in GD and that MSCs are key components of the manifestations observed in GD.</description><subject>Abnormalities</subject><subject>Adult</subject><subject>Aged</subject><subject>Analysis</subject><subject>Animals</subject><subject>Biocompatibility</subject><subject>Biology</subject><subject>Biomedical materials</subject><subject>Bone density</subject><subject>Bone marrow</subject><subject>Bone Marrow Cells - enzymology</subject><subject>Bone Marrow Cells - pathology</subject><subject>Bone mass</subject><subject>Case-Control Studies</subject><subject>Cell cycle</subject><subject>Cell Differentiation</subject><subject>Cell Proliferation</subject><subject>Cellular Microenvironment</subject><subject>Consent</subject><subject>Cytokines</subject><subject>Defects</subject><subject>Enzymes</subject><subject>Female</subject><subject>Gaucher Disease - enzymology</subject><subject>Gaucher Disease - pathology</subject><subject>Gaucher's disease</subject><subject>Glucosylceramidase</subject><subject>Glucosylceramidase - deficiency</subject><subject>Hematology</subject><subject>Hematopoiesis</subject><subject>Hematopoietic stem cells</subject><subject>Hematopoietic Stem Cells - enzymology</subject><subject>Hematopoietic Stem Cells - pathology</subject><subject>Hereditary diseases</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Mesenchymal stem cells</subject><subject>Mesenchymal Stromal Cells - enzymology</subject><subject>Mesenchymal Stromal Cells - pathology</subject><subject>Mesenchyme</subject><subject>Mice</subject><subject>Middle Aged</subject><subject>Multiple myeloma</subject><subject>Osteoblasts</subject><subject>Osteoblasts - pathology</subject><subject>Osteoclasts</subject><subject>Osteoclasts - pathology</subject><subject>Patients</subject><subject>Prospective 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prospective study of bone marrow hematopoietic and mesenchymal stem cells in type 1 Gaucher disease patients</title><author>Lecourt, Séverine ; Mouly, Enguerran ; Freida, Delphine ; Cras, Audrey ; Ceccaldi, Raphaël ; Heraoui, Djazia ; Chomienne, Christine ; Marolleau, Jean-Pierre ; Arnulf, Bertrand ; Porcher, Raphael ; Caillaud, Catherine ; Vanneaux, Valérie ; Belmatoug, Nadia ; Larghero, Jérôme</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c726t-3c2400beb76550db765ea5e8cd979c23676ecb9046134f4cd623f7b78b4935c43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Abnormalities</topic><topic>Adult</topic><topic>Aged</topic><topic>Analysis</topic><topic>Animals</topic><topic>Biocompatibility</topic><topic>Biology</topic><topic>Biomedical materials</topic><topic>Bone density</topic><topic>Bone marrow</topic><topic>Bone Marrow Cells - enzymology</topic><topic>Bone Marrow Cells - pathology</topic><topic>Bone mass</topic><topic>Case-Control Studies</topic><topic>Cell cycle</topic><topic>Cell Differentiation</topic><topic>Cell Proliferation</topic><topic>Cellular Microenvironment</topic><topic>Consent</topic><topic>Cytokines</topic><topic>Defects</topic><topic>Enzymes</topic><topic>Female</topic><topic>Gaucher Disease - enzymology</topic><topic>Gaucher Disease - pathology</topic><topic>Gaucher's disease</topic><topic>Glucosylceramidase</topic><topic>Glucosylceramidase - deficiency</topic><topic>Hematology</topic><topic>Hematopoiesis</topic><topic>Hematopoietic stem cells</topic><topic>Hematopoietic Stem Cells - enzymology</topic><topic>Hematopoietic Stem Cells - pathology</topic><topic>Hereditary diseases</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Mesenchymal stem cells</topic><topic>Mesenchymal Stromal Cells - enzymology</topic><topic>Mesenchymal Stromal Cells - pathology</topic><topic>Mesenchyme</topic><topic>Mice</topic><topic>Middle Aged</topic><topic>Multiple myeloma</topic><topic>Osteoblasts</topic><topic>Osteoblasts - pathology</topic><topic>Osteoclasts</topic><topic>Osteoclasts - pathology</topic><topic>Patients</topic><topic>Prospective Studies</topic><topic>Rodents</topic><topic>Stem cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lecourt, Séverine</creatorcontrib><creatorcontrib>Mouly, Enguerran</creatorcontrib><creatorcontrib>Freida, Delphine</creatorcontrib><creatorcontrib>Cras, Audrey</creatorcontrib><creatorcontrib>Ceccaldi, Raphaël</creatorcontrib><creatorcontrib>Heraoui, Djazia</creatorcontrib><creatorcontrib>Chomienne, Christine</creatorcontrib><creatorcontrib>Marolleau, Jean-Pierre</creatorcontrib><creatorcontrib>Arnulf, Bertrand</creatorcontrib><creatorcontrib>Porcher, Raphael</creatorcontrib><creatorcontrib>Caillaud, Catherine</creatorcontrib><creatorcontrib>Vanneaux, 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Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lecourt, Séverine</au><au>Mouly, Enguerran</au><au>Freida, Delphine</au><au>Cras, Audrey</au><au>Ceccaldi, Raphaël</au><au>Heraoui, Djazia</au><au>Chomienne, Christine</au><au>Marolleau, Jean-Pierre</au><au>Arnulf, Bertrand</au><au>Porcher, Raphael</au><au>Caillaud, Catherine</au><au>Vanneaux, Valérie</au><au>Belmatoug, Nadia</au><au>Larghero, Jérôme</au><au>Dardis, Andrea</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A prospective study of bone marrow hematopoietic and mesenchymal stem cells in type 1 Gaucher disease patients</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-07-25</date><risdate>2013</risdate><volume>8</volume><issue>7</issue><spage>e69293</spage><epage>e69293</epage><pages>e69293-e69293</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Gaucher disease (GD) is an autosomal recessive disorder characterized by lysosomal glucocerebrosidase (GBA) deficiency leading to hematological and skeletal manifestations. Mechanisms underlying these symptoms have not yet been elucidated. In vivo, bone marrow (BM) mesenchymal stem cells (MSCs) have important role in the regulation of bone mass and in the support of hematopoiesis, thus representing potential candidate that could contribute to the disease. GBA deficiency may also directly impair hematopoietic stem/progenitors cells (HSPCs) intrinsic function and induce hematological defect. In order to evaluate the role of BM stem cells in GD pathophysiology, we prospectively analyzed BM-MSCs and HSPCs properties in a series of 10 patients with type 1 GD. GBA activity was decreased in all tested cell subtypes. GD-MSCs had an impaired growth potential, morphological and cell cycle abnormalities, decreased capacities to differentiate into osteoblasts. Moreover, GD-MSCs secreted soluble factors that stimulated osteoclasts resorbing activities. In vitro and in vivo primitive and mature hematopoiesis were similar between patients and controls. However, GD-MSCs had a lower hematopoietic supportive capacity than those from healthy donors. These data suggest that BM microenvironment is altered in GD and that MSCs are key components of the manifestations observed in GD.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23935976</pmid><doi>10.1371/journal.pone.0069293</doi><tpages>e69293</tpages><orcidid>https://orcid.org/0000-0003-2086-7448</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2013-07, Vol.8 (7), p.e69293-e69293 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1427822383 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Public Library of Science (PLoS); EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Abnormalities Adult Aged Analysis Animals Biocompatibility Biology Biomedical materials Bone density Bone marrow Bone Marrow Cells - enzymology Bone Marrow Cells - pathology Bone mass Case-Control Studies Cell cycle Cell Differentiation Cell Proliferation Cellular Microenvironment Consent Cytokines Defects Enzymes Female Gaucher Disease - enzymology Gaucher Disease - pathology Gaucher's disease Glucosylceramidase Glucosylceramidase - deficiency Hematology Hematopoiesis Hematopoietic stem cells Hematopoietic Stem Cells - enzymology Hematopoietic Stem Cells - pathology Hereditary diseases Humans Life Sciences Male Medical research Medicine Mesenchymal stem cells Mesenchymal Stromal Cells - enzymology Mesenchymal Stromal Cells - pathology Mesenchyme Mice Middle Aged Multiple myeloma Osteoblasts Osteoblasts - pathology Osteoclasts Osteoclasts - pathology Patients Prospective Studies Rodents Stem cells |
title | A prospective study of bone marrow hematopoietic and mesenchymal stem cells in type 1 Gaucher disease patients |
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