4.6 Article

Estrogen depletion on In vivo osteocyte calcium signaling responses to mechanical loading

期刊

BONE
卷 152, 期 -, 页码 -

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bone.2021.116072

关键词

Osteocytes; In vivo; Estrogen loss; Mechanosensing; Ca2+ signaling

资金

  1. National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institutes of Health [AR041210, AR070547, AR073475, AG056397, DK091466, NS092466]
  2. National Institue of Aging of the National Institutes of Health [AR041210, AR070547, AR073475, AG056397, DK091466, NS092466]
  3. National Institute of Neurological Disorders and Stroke of the National Institutes of Health [AR041210, AR070547, AR073475, AG056397, DK091466, NS092466]

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The study demonstrates that ovariectomy alters the acute response of osteocytes to mechanical loading, with changes in the number, composition, and organization of osteocyte mechanosomes. Estrogen deprivation also affects the ability of osteocytes to sense small mechanical stimuli, potentially due to alterations in the structure and organization of their mechanosomes.
Microstructural adaptation of bone in response to mechanical stimuli is diminished with estrogen deprivation. Here we tested in vivo whether ovariectomy (OVX) alters the acute response of osteocytes, the principal mechanosensory cells of bone, to mechanical loading in mice. We also used super resolution microscopy (Structured Illumination microscopy or SIM) in conjunction with immunohistochemistry to assess changes in the number and organization of osteocyte mechanosomes - complexes of Panx1 channels, P2X7 receptors and CaV3 voltage-gated Ca2+ channels clustered around alpha vB3 integrin foci on osteocyte processes. Third metatarsals bones of mice expressing an osteocyte-targeted genetically encoded Ca2+ indicator (DMP1-GCaMP3) were cyclically loaded in vivo to strains from 250 to 3000 ge and osteocyte intracellular Ca2+ signaling responses were assessed in mid-diaphyses using multiphoton microscopy. The number of Ca2+ signaling osteocytes in control mice increase monotonically with applied strain magnitude for the physiological range of strains. The relationship between the number of Ca2+ signaling osteocytes and loading was unchanged at 2 days post-OVX. However, it was altered markedly at 28 days post-OVX. At loads up to 1000 ge, there was a dramatic reduction in number of responding (i.e. Ca2+ signaling) osteocytes; however, at higher strains the numbers of Ca2+ signaling osteocytes were similar to control mice. OVX significantly altered the abundance, make-up and organization of osteocyte mechanosome complexes on dendritic processes. Numbers of alpha vB3 foci also staining with either Panx 1, P2X7R or CaV3 declined by nearly half after OVX, pointing to a loss of osteocyte mechanosomes on the dendritic processes with estrogen depletion. At the same time, the areas of the remaining foci that stained for alpha vB3 and channel proteins increased significantly, a redistribution of mechanosome components suggesting a potential compensatory response. These results demonstrate that the deleterious effects of estrogen depletion on skeletal mechanical adaptation appear at the level of mechanosensation; osteocytes lose the ability to sense small (physiological) mechanical stimuli. This decline may result at least partly from changes in the structure and organization of osteocyte mechanosomes, which contribute to the distinctive sensitivity of osteocytes (particularly their dendritic processes) to mechanical stimulation.

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