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    <identifier>10.57760/sciencedb.08509</identifier>
    <datestamp>2023-06-07T14:14:30Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2023-06-07</dc:date>
  <dc:title>Salvianolic acid B accelerates osteoporotic fracture healing via lncRNA-MALAT1/miR-155-5p/HIF1A axis</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.08509</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Figure 1. SalB promotes osteogenic differentiation of hMSCs by activating MALAT1. (A) The hMSCs were subjected to osteogenic induction for 5 days, and different concentrations of SalB were added. The mRNA expression levels of MIAT, MALAT1, HOTAIR, MEG3 and H19 were evaluated by qPCR. (B-D) The hMSCs were transfected with siRNA targeting MALAT1, then the cells were treated with osteogenic induction medium with or without SalB (5 &amp;mu;M) for 7 days. The osteogenesis-related marker genes were evaluated by qPCR; (C&amp;amp;D) after 14 days of osteogenic induction, the cells were stained with Alizarin Red S, and quantified. &amp;nbsp;Figure 2. MALAT1 sponges miR-155-5p and HIF1&amp;alpha; is a bona fide target of miR-155-5p. (A) The HEK293T cells were transfected with MALAT1, empty vector, negative control (NC) or siMALAT1, then the level of mir-155-5p was quantified by qPCR. (B) The HEK293T cell lysate was incubated with biotin-labeled MALAT1. After pulldown, the miRNAs were extracted and measured by qPCR. (C) The HEK293 cells were transfected with NC, mimic or inhibitor of mir-155-5p, and the level of HIF1&amp;alpha; was quantified by qPCR. (D) Wild type (WT) and mutant (MUT) 3&amp;prime; UTR of HIF1&amp;alpha; containing the binding site with miR-155-5p was inserted into pMIR-GLO vector, respectively. The HEK293 cells were co-transfected with miRNA oligos combined with luciferase reporter (WT or MUT). Then the relative luciferase activity was measured by luciferase reporter assay and calculated. (E) Immunofluorescent detection of HIF1&amp;alpha; in hMSCs transfected with NC or mir-155-5p inhibitor.&amp;nbsp;Figure 3. SalB promoted osteoporotic fracture healing in rats. (A-C) At 6 weeks after fracture surgery, the femurs were collected for micro-CT analysis. Representative 3D images and 2D sections generated from micro-CT analysis of femurs with fracture were shown, as well as the quantitative parameters including bone volume density (BMD), and BV/TV) (n = 5). (D-F) The sections were stained with Safranin O/Fast green or HE, and the relative area of bone and uncalcified region were calculated using Image J software. (G&amp;amp;H) The mechanical properties of femurs were tested using 3-point bending test. The ultimate load and stiffness of the fractured femur were normalized with the contralateral intact femur (n = 8). *P &amp;lt; 0.05. &amp;nbsp;Figure 4. SalB increased osteogenesis and angiogenesis-related markers in the calluses. (A&amp;amp;B) The expressions of BMP2, OPN, HIF1&amp;alpha; and Runx2 in the callus were detected by immunohistological staining. (C) The H-type vessels (CD31 and EMCN positive) in the calluses were detected by immunofluorescent staining.</dc:description>
  <dc:subject>Salvianolic acid B (SalB); Osteoporotic Fracture; lncRNA-MALAT1; miR-155-5p; HIF-1α.</dc:subject>
  <dc:creator>liang</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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