Literature DB >> 16047382

Osteoblasts engulf apoptotic bodies during alveolar bone formation in the rat maxilla.

Paulo Sérgio Cerri1.   

Abstract

During bone formation, as in other tissues and organs, intense cellular proliferation and differentiation are usually observed. It has been described that programmed cell death, i.e., apoptosis, takes place in the control of the cellular population by removing of the excessive and damaged cells. Although it is generally accepted that apoptotic bodies are engulfed by professional phagocytes, the neighboring cells can also take part in the removal of apoptotic bodies. In the present study, regions of initial alveolar bone formation of rat molars were examined with the aim to verify whether osteoblasts are capable of engulfing apoptotic bodies, such as professional phagocytes. Rats aged 11-19 days were sacrificed and the maxillary fragments containing the first molar were removed and immersed in the fixative solution. The specimens fixed in glutaraldehyde-formaldehyde were processed for light microscopy and transmission electron microscopy. For the detection of apoptosis, the specimens were fixed in formaldehyde, embedded in paraffin, and submitted to the TUNEL method. The results revealed round/ovoid structures containing dense bodies on the bone surface in close contact to osteoblasts and in conspicuous osteoblast vacuoles. These round/ovoid structures showed also positivity to the TUNEL method, indicating that bone cells on the bone surface are undergoing apoptosis. Ultrathin sections showed images of apoptotic bodies being engulfed by osteoblasts. Occasionally, the osteoblasts exhibited large vacuoles containing blocks of condensed chromatin and remnants of organelles. Thus, these images suggest that osteoblasts are able to engulf and degrade apoptotic bodies. Copyright 2005 Wiley-Liss, Inc

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Year:  2005        PMID: 16047382     DOI: 10.1002/ar.a.20220

Source DB:  PubMed          Journal:  Anat Rec A Discov Mol Cell Evol Biol        ISSN: 1552-4884


  10 in total

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3.  Structural and functional changes in the alveolar bone osteoclasts of estrogen-treated rats.

Authors:  Ana Paula de Souza Faloni; Estela Sasso-Cerri; Fernanda Regina Godoy Rocha; Eduardo Katchburian; Paulo Sérgio Cerri
Journal:  J Anat       Date:  2011-11-16       Impact factor: 2.610

4.  Immunohistochemical detection of estrogen receptor beta in alveolar bone cells of estradiol-treated female rats: possible direct action of estrogen on osteoclast life span.

Authors:  Mady Crusodé de Souza; Mady Cruzoé-Souza; Estela Sasso-Cerri; Paulo S Cerri
Journal:  J Anat       Date:  2009-12       Impact factor: 2.610

5.  Apoptosis and reduced microvascular density of the lamina propria during tooth eruption in rats.

Authors:  José Paulo de Pizzol Júnior; Estela Sasso-Cerri; Paulo Sérgio Cerri
Journal:  J Anat       Date:  2015-07-30       Impact factor: 2.610

6.  Increased apoptosis in osteoclasts and decreased RANKL immunoexpression in periodontium of cimetidine-treated rats.

Authors:  Renata Longhini; Priscila Aparecida de Oliveira; Ana Paula de Souza Faloni; Estela Sasso-Cerri; Paulo Sérgio Cerri
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7.  Immunoexpression pattern of autophagy mediators in alveolar bone osteoclasts following estrogen withdrawal in female rats.

Authors:  Rinaldo Florencio-Silva; Gisela Rodrigues da Silva Sasso; Estela Sasso-Cerri; Manuel de Jesus Simões; Paulo Sérgio Cerri
Journal:  J Mol Histol       Date:  2021-01-06       Impact factor: 2.611

8.  Morphological evidences indicate that the interference of cimetidine on the peritubular components is responsible for detachment and apoptosis of Sertoli cells.

Authors:  Estela Sasso-Cerri; Paulo S Cerri
Journal:  Reprod Biol Endocrinol       Date:  2008-05-09       Impact factor: 5.211

9.  Matrix Metalloproteinase-1 and Acid Phosphatase in the Degradation of the Lamina Propria of Eruptive Pathway of Rat Molars.

Authors:  José Paulo de Pizzol Júnior; Estela Sasso-Cerri; Paulo Sérgio Cerri
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Review 10.  Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells.

Authors:  Rinaldo Florencio-Silva; Gisela Rodrigues da Silva Sasso; Estela Sasso-Cerri; Manuel Jesus Simões; Paulo Sérgio Cerri
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  10 in total

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