Increased Expression of Musashi-1 Evidences Mesenchymal Repair in Maxillary Sinus Floor Elevation.
Francisco O'ValleJuan G de BuitragoPedro Hernández-CortésMiguel Padial-MolinaVicente Crespo-LoraMarien CoboDavid AguilarPablo Galindo-MorenoPublished in: Scientific reports (2018)
This study aimed to analyze the expression of Musashi-1 (MSI1) in maxillary native bone and grafted bone after maxillary sinus floor elevation. To do so, fifty-seven bone biopsies from 45 participants were studied. Eighteen samples were collected from native bone while 39 were obtained 6 months after maxillary sinus grafting procedures. Musashi-1 was analyzed by immunohistochemistry and RT-PCR. MSI1 was detected in osteoblasts and osteocytes in 97.4% (38/39) of grafted areas. In native bone, MSI1 was detected in only 66.6% (12/18) of the biopsies, mainly in osteocytes. Detection of MSI1 was significantly higher in osteoprogenitor mesenchymal cells of grafted biopsies (p < 0.001) but minor in smooth muscle and endothelial cells; no expression was detected in adipocytes. The mesenchymal cells of the non-mineralized tissue of native bone showed very low nuclear expression of MSI1, in comparison to fusiform cells in grafted areas (0.28(0.13) vs. 2.10(0.14), respectively; p < 0.001). Additionally, the detection of MSI1 mRNA was significantly higher in biopsies from grafted areas than those from native bone (1.00(0.51) vs. 60.34(35.2), respectively; p = 0.029). Thus, our results regardig the significantly higher detection of Musashi-1 in grafted sites than in native bone reflects its importance in the remodeling/repair events that occur after maxillary sinus floor elevation in humans.
Keyphrases
- bone mineral density
- poor prognosis
- bone regeneration
- induced apoptosis
- soft tissue
- bone loss
- stem cells
- endothelial cells
- postmenopausal women
- smooth muscle
- bone marrow
- cell cycle arrest
- binding protein
- metabolic syndrome
- oxidative stress
- adipose tissue
- body composition
- cell proliferation
- cell death
- real time pcr
- long non coding rna
- skeletal muscle
- insulin resistance