Name: Murine Alveolar Bone Specimen Collection
Uploaded: 2023-07-21T12:20:00
Description: Watch this Scientific Journal Video about Murine Alveolar Bone Specimen Collection at JoVE.com

murine alveolar bone specimen collection 

Analyse du remodelage de l’os alvéolaire pour explorer la biologie mécanique squelettique

It is generally known that bone is under constant reconstruction throughout life, in response to mechanical forces according to Wolff&#39;s law1,2. Appropriate mechanical stimulation, such as gravity and daily exercise, maintains bone mass and strength and prevents bone loss by stimulating both osteoblasts and osteoclasts. Osteoclasts, responsible for bone resorption3,4,5,6,7, and osteoblasts, responsible for bone formation8,9,10, maintain bone homeostasis and function jointly in the biological process of bone remodeling. In contrast, in the absence of loading stimuli, as in astronauts under long-term microgravity, bones suffer 10% bone mineral density loss, thus increasing the risk of osteoporosis11,12. Furthermore, noninvasive and convenient mechanical therapies, including orthodontics and distraction osteogenesis, have emerged as treatments for bone diseases13,14. All these have shown that mechanical force plays a critical role in maintaining bone quality and quantity. Recent studies generally analyzed bone remodeling in response to mechanical loading using time-consuming models such as running wheel and tail suspension tests, which usually took 4 weeks or more to simulate force loading or unloading15,16. Therefore, there is demand for a convenient and efficient animal model for studying bone remodeling driven by force loading.
The alveolar bone is the most active in terms of bone remodeling, with a high turnover rate17. Orthodontic tooth movement (OTM), a common treatment for malocclusion, is an artificial process of alveolar bone remodeling in response to mechanical force. However, OTM, which induces rapid bone remodeling18, is also a time-saving way to study the effects of mechanical force on bone remodeling compared with other models with a long experimental period. Therefore, OTM is an ideal model to study bone remodeling under mechanical stimuli. It is noteworthy that the mechanism of alveolar bone remodeling is often time-sensitive, and it is necessary to observe the changes in alveolar bone remodeling at certain time points after modeling. With the dual advantages of temporal and spatial control of DNA recombination and tissue specificity, an inducible conditional gene knockout mouse model is a suitable choice for OTM studies.
Conventionally, OTM-mediated alveolar bone remodeling has been divided into tension zones involving bone formation and pressure zones involving bone resorption19,20,21, which is more detailed but difficult to regulate. Furthermore, Yuri et al. reported that the time of bone formation in OTM differed on the tension and compression sides22. In addition, a previous study had demonstrated that the first molar could initiate wide remodeling of the maxillary alveolar bone under orthodontic force, which was not constrained to the tension and pressure zones23. Therefore, we selected the area located within three roots of M1 in the cross-section of the maxillary bone as the region of interest (ROI) and described methods to assess the activity of osteoblasts and osteoclasts in the same area to evaluate alveolar bone remodeling under OTM.
As a nuclear transcription factor, signal transducer and activator of transcription 3 (STAT3) has been proven critical in bone homeostasis24,25. Previous studies have reported low bone mineral density and recurrent pathological fractures in Stat3-mutant mice26,27. Our previous study demonstrated that deletion of Stat3 in Osx+ osteoblasts caused craniofacial malformation and osteoporosis, as well as spontaneous bone fracture28. Recently, we provided in vivo evidence with an inducible osteoblast-specific Stat3 deletion mouse model (Col1&#945;2CreERT2; Stat3fl/fl, hereafter called Stat3Col1&#945;2ERT2) that STAT3 is critical in mediating the effects of orthodontic force driving alveolar bone remodeling29. In this study, we provide methods and protocols for using inducible osteoblast lineage-specific Stat3 knockout mice to study bone remodeling under orthodontic force and describe methods for analyzing alveolar bone remodeling during OTM, thus shedding light on skeletal mechanical biology.

Pleins feux sur l’auteur : Comparaison du remodelage alvéolaire et des os longs pour explorer le potentiel du modèle OTM 

Utilisation de souris knock-out Stat3 inductibles spécifiques à la lignée ostéoblastique pour étudier le remodelage osseux alvéolaire pendant le mouvement des dents orthodontiques

Our research focuses on the mechanism of bone remodeling under mechanical force, including alveolar bone and long bones. We try to answer how bones respond to mechanical stimuli to shed new light on skeletal mechanical biology for further clinical treatment. Currently, studies on OTM were limited to gene expression analysis in vivo or cellular function analysis in vitro.To this end, a challenge arose. How to trace and explore the function of specific genes in specific lineages during OTM in vivo? That's why we use inducible conditional knockout mice here.Orthodontic tooth movement, which induces rampant bone remodeling, is a time-saving method to study the effects of mechanical force on bone remodeling compared to other models that have a long experimental period. Our protocol also reveals dynamic alveolar bone remodeling at different time points with inducible gene-specific knockout mice. There are many important cell lineages in the alveolar bone.We aim to trace them and find out their underlying mechanisms during OTM. Furthermore, we will compare the mechanisms between alveolar bone and long bone remodeling to provide further clues for the potential of OTM model in biomechanical research.

Watch this Scientific Journal Video about Murine Alveolar Bone Specimen Collection at JoVE.com

Murine Alveolar Bone Specimen Collection   

Collection d’échantillons d’os alvéolaires murins 

Commencez par couper la peau verticalement de la région cervicale des souris euthanasiées, séparez la tête du corps, avec toute la peau de la tête disséquée. Ensuite, coupez la peau et les muscles buccinateurs de l’angulus oris bilatéral à la région postérieure de la mandibule. Déconnectez complètement les muscles buccaux et les tendons des coracoïdes pour retirer la mandibule.Coupez tous les os supplémentaires pour obtenir les maxillaires complets. Retirez l’os derrière les troisièmes molaires bilatérales et décollez la muqueuse palatine. Enfin, débranchez l’appareil orthodontique et coupez l’os entre les incisives le long de la suture palatine médiane pour obtenir l’os alvéolaire droit et gauche.Le remodelage osseux alvéolaire dans la délétion de STAT3 dans les ostéoblastes a été confirmé par une coloration immunofluorescente de l’os alvéolaire. La stéréomicroscopie a révélé que la distance de déplacement orthodontique des dents des souris de type sauvage augmentait aux jours quatre, sept et dix. Cependant, la distance de déplacement des dents orthodontiques a été réduite chez les souris knock-out STAT3.L’analyse micro-TDM du jour 10 a confirmé la réduction des mouvements, indiquant que la délétion STAT3 ralentissait le mouvement des dents orthodontiques.

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Medicine

Murine Alveolar Bone Specimen Collection 

Using Inducible Osteoblastic Lineage-Specific Stat3 Knockout Mice to Study Alveolar Bone Remodeling During Orthodontic Tooth Movement

The alveolar bone, with a high turnover rate, is the most actively-remodeling bone in the body. Orthodontic tooth movement (OTM) is a common artificial ...