scholarly journals In vivo Labeling of Bone Microdamage in an Animal Model of Type 1 Diabetes Mellitus

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Sahar Mohsin ◽  
Suneesh Kaimala ◽  
Eman Khamis Yousef AlTamimi ◽  
Saeed Tariq ◽  
Ernest Adeghate

AbstractType 1 diabetes mellitus (DM1) is linked to a decrease in bone strength. Bone strength entails both bone mineral density and bone quality. Limited data are available regarding diabetes-induced microdamage, which can severely influence bone quality. This study has investigated bone microdamage as a measure of bone quality in an animal model of DM1. Microdamage in the neck of the femur was labelled in vivo using multiple fluorochromes at 4, 12 and 24 weeks after the onset of DM1. Microcracks were quantified and their morphology analyzed using microscopy techniques. The mean length of microcracks at 24 weeks, and crack numerical and surface densities were significantly higher (p < 0.05) 4 weeks after the onset of DM1 when compared with control. Diffuse damage density was highest at 12 weeks after the onset of DM1. The arrangement of the collagen fibrils became progressively more irregular from 4 to 24 weeks of DM. This is the first study to analyze microdamage in vivo at different time points of DM1. DM1is associated with microcracks from the early stage, however bone microstructure shows toughening mechanisms that arrest their growth but disease progression further deteriorates bone quality resulting in longer microcracks which may increase fracture risk.

2019 ◽  
Vol 47 (1) ◽  
pp. 721-726 ◽  
Author(s):  
Michelle T. Alves ◽  
Amanda C. S. Chaves ◽  
Ana Paula M. Almeida ◽  
Ana Cristina Simões e Silva ◽  
Stanley de A. Araújo ◽  
...  

2019 ◽  
Vol 5 (1) ◽  
Author(s):  
Rongze Wang ◽  
Yuanxu Zhang ◽  
Fujun Jin ◽  
Gongchen Li ◽  
Yao Sun ◽  
...  

Abstract Type 1 diabetes mellitus (T1DM) is an autoimmune insulin-dependent disease associated with destructive bone homeostasis. Accumulating evidence has proven that miRNAs are widely involved in the regulation of bone homeostasis. However, whether miRNAs also regulate osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) in T1DM mice is under exploration. In this study, miRNA microarray was utilized to screen the differentially expressed miRNAs, which uncovered that miR-214-3p potentially inhibited BMSCs osteogenic differentiation in T1DM mice. We found that high glucose suppressed BMSCs osteogenic differentiation with significant elevation of the miR-214-3p expression. Further study found that the osteogenic differentiation of BMSCs was inhibited by AgomiR-214-3p while enhanced by AntagomiR-214-3p in BMSCs supplemented with high glucose. Moreover, we found that miR-214-3p knockout T1DM mice were resistant to high-glucose-induced bone loss. These results provide a novel insight into an inhibitory role of high-glucose-induced miR-214-3p in BMSCs osteogenic differentiation both in vitro and in vivo. Molecular studies revealed that miR-214-3p inhibits BMSCs osteogenic differentiation by targeting the 3′-UTR of β-catenin, which was further corroborated in human bone specimens and BMSCs of T1DM patients. Taken together, our study discovered that miR-214-3p is a pivotal regulator of BMSCs osteogenic differentiation in T1DM mice. Our findings also suggest that miR-214-3p could be a potential target in the treatment of bone disorders in patients with T1DM.


2010 ◽  
Vol 42 ◽  
pp. 728
Author(s):  
Marcelo Ferreina Novelino ◽  
Muiara Aparecida Morais ◽  
Dihogo Gama Mattos ◽  
Raúl Marcel Gonzalez Garcia

2015 ◽  
Vol 10 (3) ◽  
pp. 300-305 ◽  
Author(s):  
Khalid I. Khoshhal ◽  
Salah A. Sheweita ◽  
Mohammad S. Al-Maghamsi ◽  
Abdelhadi M. Habeb

2021 ◽  
Author(s):  
Catharina Barros Pimentel Villaça ◽  
Carolina Cavalcante Paula ◽  
Caroline Cruz Oliveira ◽  
Eloisa Aparecida Vilas‐Boas ◽  
Junia Carolina Santos‐Silva ◽  
...  

1989 ◽  
Vol 52 (3) ◽  
pp. 406-413 ◽  
Author(s):  
Liisa Räsänen ◽  
H. Hyöty ◽  
Maili Lehto ◽  
O.-P. Kallioniemi ◽  
Tuula Huupponen ◽  
...  

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