Reduced Osteoclastogenesis and RANKL Expression in Marrow from Women Taking Alendronate
Alendronate (AL) is commonly used for the prevention and treatment of osteoporotic fractures. Little is known about the effects of AL administration on osteoclast differentiation from human marrow progenitor cells. We used marrow discarded during orthopedic surgery to test the hypothesis that cultur...
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Published in | Calcified tissue international Vol. 88; no. 4; pp. 272 - 280 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer-Verlag
01.04.2011
Springer Nature B.V |
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Abstract | Alendronate (AL) is commonly used for the prevention and treatment of osteoporotic fractures. Little is known about the effects of AL administration on osteoclast differentiation from human marrow progenitor cells. We used marrow discarded during orthopedic surgery to test the hypothesis that cultures of bone marrow-derived stem cells (BMCs) from subjects receiving AL (+AL) may differ from control subjects with respect to in vitro osteoclast differentiation and regulatory factors. The number of osteoclasts generated in BMC cultures from control subjects was 4.7-fold greater than that from +AL subjects (
P
= 0.015). RANKL expression in +AL BMCs was 57% of that in controls (
P
= 0.001), and OPG expression in +AL BMCs was greater than in controls (153%,
P
= 0.01). The mean RANKL/OPG ratio in BMCs was 0.65 ± 0.35 for +AL specimens and 1.28 ± 0.53 for controls (
P
= 0.031). In addition, we assessed the direct effect of AL on expression of RANKL and OPG in marrow stromal cells isolated from nine control women. Treatment with AL downregulated RANKL expression and upregulated OPG expression, with an average 50% decrease in RANKL/OPG ratio at 10
−7
M (
P
= 0.004). These results show that osteoclast differentiation is dysregulated in marrow isolated from +AL subjects. Furthermore, AL may inhibit human osteoclastogenesis by affecting the key regulatory genes in marrow cells. |
---|---|
AbstractList | Alendronate (AL) is commonly used for the prevention and treatment of osteoporotic fractures. Little is known about the effects of AL administration on osteoclast differentiation from human marrow progenitor cells. We used marrow discarded during orthopedic surgery to test the hypothesis that cultures of bone marrow-derived stem cells (BMCs) from subjects receiving AL (+AL) may differ from control subjects with respect to in vitro osteoclast differentiation and regulatory factors. The number of osteoclasts generated in BMC cultures from control subjects was 4.7-fold greater than that from +AL subjects (P = 0.015). RANKL expression in +AL BMCs was 57% of that in controls (P = 0.001), and OPG expression in +AL BMCs was greater than in controls (153%, P = 0.01). The mean RANKL/OPG ratio in BMCs was 0.65 ± 0.35 for +AL specimens and 1.28 ± 0.53 for controls (P = 0.031). In addition, we assessed the direct effect of AL on expression of RANKL and OPG in marrow stromal cells isolated from nine control women. Treatment with AL downregulated RANKL expression and upregulated OPG expression, with an average 50% decrease in RANKL/OPG ratio at 10(-7) M (P = 0.004). These results show that osteoclast differentiation is dysregulated in marrow isolated from +AL subjects. Furthermore, AL may inhibit human osteoclastogenesis by affecting the key regulatory genes in marrow cells. Alendronate (AL) is commonly used for the prevention and treatment of osteoporotic fractures. Little is known about the effects of AL administration on osteoclast differentiation from human marrow progenitor cells. We used marrow discarded during orthopedic surgery to test the hypothesis that cultures of bone marrow-derived stem cells (BMCs) from subjects receiving AL (+AL) may differ from control subjects with respect to in vitro osteoclast differentiation and regulatory factors. The number of osteoclasts generated in BMC cultures from control subjects was 4.7-fold greater than that from +AL subjects (P = 0.015). RANKL expression in +AL BMCs was 57% of that in controls (P = 0.001), and OPG expression in +AL BMCs was greater than in controls (153%, P = 0.01). The mean RANKL/OPG ratio in BMCs was 0.65 ± 0.35 for +AL specimens and 1.28 ± 0.53 for controls (P = 0.031). In addition, we assessed the direct effect of AL on expression of RANKL and OPG in marrow stromal cells isolated from nine control women. Treatment with AL downregulated RANKL expression and upregulated OPG expression, with an average 50% decrease in RANKL/OPG ratio at 10^sup -7^ M (P = 0.004). These results show that osteoclast differentiation is dysregulated in marrow isolated from +AL subjects. Furthermore, AL may inhibit human osteoclastogenesis by affecting the key regulatory genes in marrow cells.[PUBLICATION ABSTRACT] Alendronate (AL) is commonly used for the prevention and treatment of osteoporotic fractures. Little is known about the effects of AL administration on osteoclast differentiation from human marrow progenitor cells. We used marrow discarded during orthopedic surgery to test the hypothesis that cultures of bone marrow-derived stem cells (BMCs) from subjects receiving AL (+AL) may differ from control subjects with respect to in vitro osteoclast differentiation and regulatory factors. The number of osteoclasts generated in BMC cultures from control subjects was 4.7-fold greater than that from +AL subjects (P = 0.015). RANKL expression in +AL BMCs was 57% of that in controls (P = 0.001), and OPG expression in +AL BMCs was greater than in controls (153%, P = 0.01). The mean RANKL/OPG ratio in BMCs was 0.65 ± 0.35 for +AL specimens and 1.28 ± 0.53 for controls (P = 0.031). In addition, we assessed the direct effect of AL on expression of RANKL and OPG in marrow stromal cells isolated from nine control women. Treatment with AL downregulated RANKL expression and upregulated OPG expression, with an average 50% decrease in RANKL/OPG ratio at 10(-7) M (P = 0.004). These results show that osteoclast differentiation is dysregulated in marrow isolated from +AL subjects. Furthermore, AL may inhibit human osteoclastogenesis by affecting the key regulatory genes in marrow cells.Alendronate (AL) is commonly used for the prevention and treatment of osteoporotic fractures. Little is known about the effects of AL administration on osteoclast differentiation from human marrow progenitor cells. We used marrow discarded during orthopedic surgery to test the hypothesis that cultures of bone marrow-derived stem cells (BMCs) from subjects receiving AL (+AL) may differ from control subjects with respect to in vitro osteoclast differentiation and regulatory factors. The number of osteoclasts generated in BMC cultures from control subjects was 4.7-fold greater than that from +AL subjects (P = 0.015). RANKL expression in +AL BMCs was 57% of that in controls (P = 0.001), and OPG expression in +AL BMCs was greater than in controls (153%, P = 0.01). The mean RANKL/OPG ratio in BMCs was 0.65 ± 0.35 for +AL specimens and 1.28 ± 0.53 for controls (P = 0.031). In addition, we assessed the direct effect of AL on expression of RANKL and OPG in marrow stromal cells isolated from nine control women. Treatment with AL downregulated RANKL expression and upregulated OPG expression, with an average 50% decrease in RANKL/OPG ratio at 10(-7) M (P = 0.004). These results show that osteoclast differentiation is dysregulated in marrow isolated from +AL subjects. Furthermore, AL may inhibit human osteoclastogenesis by affecting the key regulatory genes in marrow cells. Alendronate (AL) is commonly used for prevention and treatment of osteoporotic fractures. Little is known about the effects of AL administration on osteoclast differentiation from human marrow progenitor cells. We used marrow discarded during orthopedic surgery to test the hypothesis that cultures of bone marrow-derived stem cells (BMCs) from subjects receiving AL (+AL) may differ from control subjects with respect to in vitro osteoclast differentiation and regulatory factors. The number of osteoclasts generated in BMC cultures from control subjects was 4.7-fold greater than +AL subjects (p = 0.015). The expression of RANKL in +AL BMCs was 57% of that in controls (p = 0.001), and the expression of OPG in +AL BMCs was greater than in controls (153%, p = 0.01). The mean RANKL/OPG ratio in BMCs was 0.65 ± 0.35 for +AL specimens and 1.28 ± 0.53 for Controls (p = 0.031). In addition, we assessed the direct effect of AL on expression of RANKL and OPG in marrow stromal cells isolated from 9 control women. Treatment with AL downregulated RANKL expression and upregulated expression of OPG, with an average 50% decrease in RANKL/OPG ratio at 10 −7 M (p = 0.004). These studies show that osteoclast differentiation is dysregulated in marrow isolated from +AL subjects. Furthermore, these results demonstrate that AL may inhibit human osteoclastogenesis by affecting the key regulatory genes in marrow cells. Alendronate (AL) is commonly used for the prevention and treatment of osteoporotic fractures. Little is known about the effects of AL administration on osteoclast differentiation from human marrow progenitor cells. We used marrow discarded during orthopedic surgery to test the hypothesis that cultures of bone marrow-derived stem cells (BMCs) from subjects receiving AL (+AL) may differ from control subjects with respect to invitro osteoclast differentiation and regulatory factors. The number of osteoclasts generated in BMC cultures from control subjects was 4.7-fold greater than that from +AL subjects (P=0.015). RANKL expression in +AL BMCs was 57% of that in controls (P=0.001), and OPG expression in +AL BMCs was greater than in controls (153%, P=0.01). The mean RANKL/OPG ratio in BMCs was 0.65 plus or minus 0.35 for +AL specimens and 1.28 plus or minus 0.53 for controls (P=0.031). In addition, we assessed the direct effect of AL on expression of RANKL and OPG in marrow stromal cells isolated from nine control women. Treatment with AL downregulated RANKL expression and upregulated OPG expression, with an average 50% decrease in RANKL/OPG ratio at 10 super(-7) M (P=0.004). These results show that osteoclast differentiation is dysregulated in marrow isolated from +AL subjects. Furthermore, AL may inhibit human osteoclastogenesis by affecting the key regulatory genes in marrow cells. Alendronate (AL) is commonly used for the prevention and treatment of osteoporotic fractures. Little is known about the effects of AL administration on osteoclast differentiation from human marrow progenitor cells. We used marrow discarded during orthopedic surgery to test the hypothesis that cultures of bone marrow-derived stem cells (BMCs) from subjects receiving AL (+AL) may differ from control subjects with respect to in vitro osteoclast differentiation and regulatory factors. The number of osteoclasts generated in BMC cultures from control subjects was 4.7-fold greater than that from +AL subjects ( P = 0.015). RANKL expression in +AL BMCs was 57% of that in controls ( P = 0.001), and OPG expression in +AL BMCs was greater than in controls (153%, P = 0.01). The mean RANKL/OPG ratio in BMCs was 0.65 ± 0.35 for +AL specimens and 1.28 ± 0.53 for controls ( P = 0.031). In addition, we assessed the direct effect of AL on expression of RANKL and OPG in marrow stromal cells isolated from nine control women. Treatment with AL downregulated RANKL expression and upregulated OPG expression, with an average 50% decrease in RANKL/OPG ratio at 10 −7 M ( P = 0.004). These results show that osteoclast differentiation is dysregulated in marrow isolated from +AL subjects. Furthermore, AL may inhibit human osteoclastogenesis by affecting the key regulatory genes in marrow cells. |
Author | Zhou, Shuanhu LeBoff, Meryl S. Van Eekeren, Inge Eslami, Behnam Glowacki, Julie |
AuthorAffiliation | c Department of Oral & Maxillofacial Surgery, Harvard School of Dental Medicine, Boston, MA a Department of Orthopedic Surgery, Brigham and Women Hospital and Harvard Medical School, Boston, MA b Division of Endocrinology, Brigham and Women Hospital and Harvard Medical School, Boston, MA |
AuthorAffiliation_xml | – name: a Department of Orthopedic Surgery, Brigham and Women Hospital and Harvard Medical School, Boston, MA – name: c Department of Oral & Maxillofacial Surgery, Harvard School of Dental Medicine, Boston, MA – name: b Division of Endocrinology, Brigham and Women Hospital and Harvard Medical School, Boston, MA |
Author_xml | – sequence: 1 givenname: Behnam surname: Eslami fullname: Eslami, Behnam organization: Department of Orthopedic Surgery, Brigham and Women Hospital and Harvard Medical School – sequence: 2 givenname: Shuanhu surname: Zhou fullname: Zhou, Shuanhu organization: Department of Orthopedic Surgery, Brigham and Women Hospital and Harvard Medical School – sequence: 3 givenname: Inge surname: Van Eekeren fullname: Van Eekeren, Inge organization: Department of Orthopedic Surgery, Brigham and Women Hospital and Harvard Medical School – sequence: 4 givenname: Meryl S. surname: LeBoff fullname: LeBoff, Meryl S. organization: Division of Endocrinology, Brigham and Women Hospital and Harvard Medical School – sequence: 5 givenname: Julie surname: Glowacki fullname: Glowacki, Julie email: jglowacki@rics.bwh.harvard.edu organization: Department of Orthopedic Surgery, Brigham and Women Hospital and Harvard Medical School, Department of Oral & Maxillofacial Surgery, Harvard School of Dental Medicine |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/21327765$$D View this record in MEDLINE/PubMed |
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Keywords | Bisphosphonate RANKL Osteoclast Alendronate OPG |
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Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 This work was conducted in partial fulfillment for the D.M.Sc. in Oral Biology and for Certification in Oral and Maxillofacial Pathology from the Harvard School of Dental Medicine |
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Snippet | Alendronate (AL) is commonly used for the prevention and treatment of osteoporotic fractures. Little is known about the effects of AL administration on... Alendronate (AL) is commonly used for prevention and treatment of osteoporotic fractures. Little is known about the effects of AL administration on osteoclast... |
SourceID | pubmedcentral proquest pubmed crossref springer |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 272 |
SubjectTerms | Aged, 80 and over Alendronate - pharmacology Biochemistry Biomedical and Life Sciences Bone marrow Bone Marrow Cells - cytology Case-Control Studies Cell Biology Cell Differentiation Cellular biology Diphosphonates - pharmacology Drug therapy Endocrinology Female Gene Expression Regulation Humans Life Sciences Original Research Orthopedics Osteoclasts - cytology Osteoporosis Osteoporosis, Postmenopausal - prevention & control Osteoprotegerin - biosynthesis Pharmacology RANK Ligand - biosynthesis Stem Cells - cytology |
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Title | Reduced Osteoclastogenesis and RANKL Expression in Marrow from Women Taking Alendronate |
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