Morphological Study of Bone Cranial in Athymic Mice

The aim of our research was to create an osteogenic unit in the skulls of athymic mice; however, the first challenge we faced was to find sufficient and adequate data that would allow us to determine the morphological, immunohistochemical and microtopographical characteristics that could be used as...

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Autores principales: Sesman,Ana, Ruvalcaba,Erika, Herrera,Arturo, Sánchez Guerrero,Sergio, Lecona,Hugo, Baena-Ocampo,Leticia, Solis,Lilia, Ávila,Hector, García de la Puente,Silvestre, Vargas,Betha, Guerrero,Xochitl, Velasquillo,Cristina
Lenguaje:English
Publicado: Sociedad Chilena de Anatomía 2013
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022013000100050
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spelling oai:scielo:S0717-950220130001000502014-09-09Morphological Study of Bone Cranial in Athymic MiceSesman,AnaRuvalcaba,ErikaHerrera,ArturoSánchez Guerrero,SergioLecona,HugoBaena-Ocampo,LeticiaSolis,LiliaÁvila,HectorGarcía de la Puente,SilvestreVargas,BethaGuerrero,XochitlVelasquillo,Cristina Osteogenesis Osteoinduction Osteoconductivity The aim of our research was to create an osteogenic unit in the skulls of athymic mice; however, the first challenge we faced was to find sufficient and adequate data that would allow us to determine the morphological, immunohistochemical and microtopographical characteristics that could be used as normality standards in athymic mice skulls and, hence, a reference in the event of achieving the formation of de novo bone using the osteogenic unit we proposed. Knowing the normal bone morphology in the skull of athymic mice was a necessary precondition to develop subsequently an osteogenic unit possessing the Osteogenesis, Osteoinduction and Osteoconductivity that could be compared versus those in the normal bone during its formations and remodeling processes. Therefore, we conducted a pilot study to determine bone morphological characteristics in the skull of athymic mice by means of specific histological staining: hematoxylin-eosin and Von Kossa, for osteoid tissue and mineralized bone, and Masson Tri-chrome for ossified areas. We also use immunohistochemistry to detect bone formation markers: alkaline phosphatase resulting from osteoblastic activity stimulation, type 1 collagen a bonematrix structural protein; Osteopontine, a protein specifically synthesized by osteoblasts that favors cell proliferation and remodeling in bone defects; Osteocalcine, a peptide hormone produced by osteoblasts during bone formation; and, Runx 2, a transcription factor expressed by stem cells which stimulates bone differentiation. Likewise, we used electron microscopy on the newly formed tissue to determine the presence of organic deposits, such as calcium, phosphate and magnesium in bone tissue.info:eu-repo/semantics/openAccessSociedad Chilena de AnatomíaInternational Journal of Morphology v.31 n.1 20132013-03-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022013000100050en10.4067/S0717-95022013000100050
institution Scielo Chile
collection Scielo Chile
language English
topic Osteogenesis
Osteoinduction
Osteoconductivity
spellingShingle Osteogenesis
Osteoinduction
Osteoconductivity
Sesman,Ana
Ruvalcaba,Erika
Herrera,Arturo
Sánchez Guerrero,Sergio
Lecona,Hugo
Baena-Ocampo,Leticia
Solis,Lilia
Ávila,Hector
García de la Puente,Silvestre
Vargas,Betha
Guerrero,Xochitl
Velasquillo,Cristina
Morphological Study of Bone Cranial in Athymic Mice
description The aim of our research was to create an osteogenic unit in the skulls of athymic mice; however, the first challenge we faced was to find sufficient and adequate data that would allow us to determine the morphological, immunohistochemical and microtopographical characteristics that could be used as normality standards in athymic mice skulls and, hence, a reference in the event of achieving the formation of de novo bone using the osteogenic unit we proposed. Knowing the normal bone morphology in the skull of athymic mice was a necessary precondition to develop subsequently an osteogenic unit possessing the Osteogenesis, Osteoinduction and Osteoconductivity that could be compared versus those in the normal bone during its formations and remodeling processes. Therefore, we conducted a pilot study to determine bone morphological characteristics in the skull of athymic mice by means of specific histological staining: hematoxylin-eosin and Von Kossa, for osteoid tissue and mineralized bone, and Masson Tri-chrome for ossified areas. We also use immunohistochemistry to detect bone formation markers: alkaline phosphatase resulting from osteoblastic activity stimulation, type 1 collagen a bonematrix structural protein; Osteopontine, a protein specifically synthesized by osteoblasts that favors cell proliferation and remodeling in bone defects; Osteocalcine, a peptide hormone produced by osteoblasts during bone formation; and, Runx 2, a transcription factor expressed by stem cells which stimulates bone differentiation. Likewise, we used electron microscopy on the newly formed tissue to determine the presence of organic deposits, such as calcium, phosphate and magnesium in bone tissue.
author Sesman,Ana
Ruvalcaba,Erika
Herrera,Arturo
Sánchez Guerrero,Sergio
Lecona,Hugo
Baena-Ocampo,Leticia
Solis,Lilia
Ávila,Hector
García de la Puente,Silvestre
Vargas,Betha
Guerrero,Xochitl
Velasquillo,Cristina
author_facet Sesman,Ana
Ruvalcaba,Erika
Herrera,Arturo
Sánchez Guerrero,Sergio
Lecona,Hugo
Baena-Ocampo,Leticia
Solis,Lilia
Ávila,Hector
García de la Puente,Silvestre
Vargas,Betha
Guerrero,Xochitl
Velasquillo,Cristina
author_sort Sesman,Ana
title Morphological Study of Bone Cranial in Athymic Mice
title_short Morphological Study of Bone Cranial in Athymic Mice
title_full Morphological Study of Bone Cranial in Athymic Mice
title_fullStr Morphological Study of Bone Cranial in Athymic Mice
title_full_unstemmed Morphological Study of Bone Cranial in Athymic Mice
title_sort morphological study of bone cranial in athymic mice
publisher Sociedad Chilena de Anatomía
publishDate 2013
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022013000100050
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