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 inCalcified tissue international Vol. 88; no. 4; pp. 272 - 280
Main Authors Eslami, Behnam, Zhou, Shuanhu, Van Eekeren, Inge, LeBoff, Meryl S., Glowacki, Julie
Format Journal Article
LanguageEnglish
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
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  surname: Eslami
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  organization: Department of Orthopedic Surgery, Brigham and Women Hospital and Harvard Medical School
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  givenname: Shuanhu
  surname: Zhou
  fullname: Zhou, Shuanhu
  organization: Department of Orthopedic Surgery, Brigham and Women Hospital and Harvard Medical School
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  givenname: Inge
  surname: Van Eekeren
  fullname: Van Eekeren, Inge
  organization: Department of Orthopedic Surgery, Brigham and Women Hospital and Harvard Medical School
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  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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1432-0827
IngestDate Thu Aug 21 13:59:07 EDT 2025
Fri Jul 11 02:07:55 EDT 2025
Mon Jul 21 11:57:23 EDT 2025
Fri Jul 25 19:16:31 EDT 2025
Mon Jul 21 05:56:34 EDT 2025
Tue Jul 01 05:19:00 EDT 2025
Thu Apr 24 23:01:12 EDT 2025
Fri Feb 21 02:44:37 EST 2025
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Issue 4
Keywords Bisphosphonate
RANKL
Osteoclast
Alendronate
OPG
Language English
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content type line 14
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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...
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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
URI https://link.springer.com/article/10.1007/s00223-011-9473-5
https://www.ncbi.nlm.nih.gov/pubmed/21327765
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Volume 88
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