PubMed · 14809141
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P ROBERT. [Painful malacic decalcification].. https://pubmed.ncbi.nlm.nih.gov/14809141/
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We isolated dental papilla from impacted human molar and proliferated adherent fibroblastic cells after collagenase treatment of the papilla. The cells were negative for hematopoietic markers but positive for CD29, CD44, CD90, CD105, and CD166. When the cells were further cultured in the presence of beta-glycerophosphate, ascorbic acid, and dexamethasone for 14 days, mineralized areas together with osteogenic differentiation evidenced by high alkaline phosphatase activity and osteocalcin contents were observed. The differentiation was confirmed at both protein and gene expression levels. The cells can also be cryopreserved and, after thawing, could show in vivo bone-forming capability. These results indicate that mesenchymal type cells localize in dental papilla and that the cells can be culture expanded/utilized for bone tissue engineering.
Mammograms taken by two views: cranio-caudal (CC) and medio-lateral oblique (MLO) views provide only 2D projections of the microcalcifications, which lack the depth information. Thus, envisioning the relative lesion location from mammograms is a challenge for radiologists. To assist radiologists in locating and rendering lesion tissues, a modified projective grid space (MPGS) scheme is proposed to reconstruct 3D microcalcifications. The MPGS scheme reconstructs 3D microcalcifications in a unique space defined by corresponding points and the epipoles retrieved from the fundamental matrix of the CC and MLO views. Since only corresponding points of images are required in the proposed MPGS scheme, we can avoid the difficulty associated with most reconstruction approaches that require prior complicated calibration of X-ray machine. Considering the deformation of the breast, a new method based on the concept of bundle adjustment is proposed to rectify the 3D locations of reconstructed microcalcifications by uncompressed breast model reconstructed from the real patient body using MPGS scheme with iterative closest point (ICP). Then, the reconstructed microcalcifications are augmented in the real patient body model to show their relative positions.
We studied the effect of calcite encrustation in stoneworts (Chara spp.) on P cycling in an aquatic ecosystem. Sequential fractionation was performed to quantify P fractions of the internodes of calcified (Ca-CF) and uncalcified (UCa-CF) Chara fibrosa Agardh ex Bruzelius. Our results showed that Ca-CF was able to store more P and about 14 to 23% of total P in Ca-CF was co-precipitated with encrusted calcite, while only 2 to 3% was found in UCa-CF. Furthermore, in Ca-CF, an increased amount of total P did not result in a higher release of bioavailable water-soluble and sodium hydroxide-extractable P. Extracellular calcification in Chara enhanced nutrient sink for P, provided a further bottom-up control of phytoplankton, and should be regarded as a positive feedback in stabilizing Chara dominance in lakes.