Literature DB >> 10593411

Isolation and hormonal responsiveness of primary cultures of human bone-derived cells: gender and age differences.

S Katzburg1, M Lieberherr, A Ornoy, B Y Klein, D Hendel, D Somjen.   

Abstract

We present a model for isolating human cell culture derived from biopsies obtained during orthopedic surgery. Four donor groups were defined by gender and age: pre- and postmenopausal women (<50 and >55 years, respectively), and younger (30-55 years) and older (>60 years) men. Bone-derived cells were identified as osteoblasts by major osteoblastic characteristics; that is, high alkaline phosphatase (ALP) activity, dose-dependent increase of ALP by 1,25(OH)2D3, high levels of parathyroid hormone (PTH)-induced cyclic AMP, and 1,25-(OH)2D3-induced osteocalcin. In all cells, levels of osteocalcin were significantly elevated (p < 0.05 and 0.01). In cells derived from men, no significant age differences were found in ALP and osteocalcin values of basal activity and in fold stimulation 1,25(OH)2D3. Cells from postmenopausal women showed a nonsignificant lower basal ALP activity than premenopausal cells. In postmenopausal cells, ALP responded less to 1,25(OH)2D3 (33% increase, p < 0.05) than the premenopausal cells (100% increase, p < 0.05). In cells from either age group, ALP did not respond to the gonadal steroids 17beta-estradiol (E2) and dihydrotestosterone (DHT) or progesterone. Basal levels of osteocalcin were higher in cells of premenopausal origin as compared with postmenopausal cells (p = 0.05), but response to 1,25(OH)2D3 was the same. PTH significantly stimulated cAMP (p = 0.001) in all age and gender groups analyzed. In all groups, no differences were found in either basal activity or in PTH response. Unlike men, cells derived from the bone of women were more susceptible to age changes. We postulate that the postmenopausal cell population had a decreased number of osteoblasts, or cells in a lower differentiation stage. These results extend our knowledge of bone biology found in animal models and reveal that human osteoblasts from men do not show the same age-dependent differences observed in women.

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Year:  1999        PMID: 10593411     DOI: 10.1016/s8756-3282(99)00225-2

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  11 in total

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3.  Age and gender specific stimulation of creatine kinase specific activity by gonadal steroids in human bone-derived cells in culture.

Authors:  S Katzburg; A Ornoy; D Hendel; M Lieberherr; A M Kaye; D Somjen
Journal:  J Endocrinol Invest       Date:  2001-03       Impact factor: 4.256

4.  Decreased response of osteoblasts obtained from aged Cohen diabetic sensitive rats to sex steroid hormones and 1,25OH2D3 in culture.

Authors:  Asher Ornoy; Perchia Yaffe; Sarah W Zangen; Nathan Patlas; Zvi Schwartz
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5.  Efficacy and safety of DT56a compared to hormone therapy in Greek post-menopausal women.

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Journal:  J Endocrinol Invest       Date:  2013-04-08       Impact factor: 4.256

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Review 9.  Molecular Basis of Bone Aging.

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Journal:  Int J Mol Sci       Date:  2020-05-23       Impact factor: 5.923

Review 10.  Let's Talk About Sex-Biological Sex Is Underreported in Biomaterial Studies.

Authors:  Bryan D James; Paxton Guerin; Josephine B Allen
Journal:  Adv Healthc Mater       Date:  2020-10-11       Impact factor: 9.933

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