27 research outputs found
Neuromatch Academy: Teaching Computational Neuroscience with global accessibility
Neuromatch Academy designed and ran a fully online 3-week Computational
Neuroscience summer school for 1757 students with 191 teaching assistants
working in virtual inverted (or flipped) classrooms and on small group
projects. Fourteen languages, active community management, and low cost allowed
for an unprecedented level of inclusivity and universal accessibility.Comment: 10 pages, 3 figures. Equal contribution by the executive committee
members of Neuromatch Academy: Tara van Viegen, Athena Akrami, Kate Bonnen,
Eric DeWitt, Alexandre Hyafil, Helena Ledmyr, Grace W. Lindsay, Patrick
Mineault, John D. Murray, Xaq Pitkow, Aina Puce, Madineh Sedigh-Sarvestani,
Carsen Stringer. and equal contribution by the board of directors of
Neuromatch Academy: Gunnar Blohm, Konrad Kording, Paul Schrater, Brad Wyble,
Sean Escola, Megan A. K. Peter
Fault Zone Development with Temporal Impact on Fluid Flow - Example from Navajo Sandstone, Utah
Comparison of the Effect of Adipocyte-derived Stem Cells and Curcumin Nanoliposomes with Phenytoin on Open Cutaneous Wound Healing in Rats
Background:
Reducing the healing time of wounds can decrease the patient's immobility
time and their medical costs, leading a faster return of the patients to daily work.
Objective:
The aim of the present study is to compare the effect of adipose-derived stem cells and curcumin-
containing liposomal nanoparticles with phenytoin on wound healing.
Methods:
After anesthesia of the rats, open skin ulcers were made by a bistoury blade. Subsequently,
stem cells were removed from the adipose tissue of the upper border of the epididymis. The originality
of stem cells was then confirmed by the flow cytometry. The fusion method was used to prepare the
liposome; and also, nanoliposomal particles were confirmed by using the DLS microscope. The percentage
of recovery and the cell count was measured with IMAGEJ. The expression of genes was assessed
by PCR. The number of fibroblasts was counted by immunohistochemistry techniques. The
amount of collagen was determined by Tri-chromosome staining, and the number of capillaries was
enumerated by H & E staining.
Results:
The expression of the TGF-β1 gene, vascular number, wound healing rate and the number of
fibroblasts increased significantly in adipose tissue-derived stem cells and curcumin nanoliposome
groups (p<0.05); the wound surface was also decreased significantly (p<0.05).
Conclusion:
Based on the results of our research, adipose tissue-derived stem cells and curcumin
nanoliposomes can heal wounds efficiently.
</jats:sec
Experimental Study of Modeling Partially Drained Dense Sand Behavior in Monotonic Triaxial Compression Loading Tests
The Effects of Strain Localization on the Determination of Critical State Seen with Experimental and Numerical Models
Developing a multiple-criteria decision analysis for green economy transition: a Canadian case study
Strain localization in sandstone and its implications for CO2 storage
International audienc
CAR T-cell-mediated delivery of bispecific innate immune cell engagers for neuroblastoma
Abstract Novel chimeric antigen receptor (CAR) T-cell approaches are needed to improve therapeutic efficacy in solid tumors. High-risk neuroblastoma is an aggressive pediatric solid tumor that expresses cell-surface GPC2 and GD2 with a tumor microenvironment infiltrated by CD16a-expressing innate immune cells. Here we engineer T-cells to express a GPC2-directed CAR and simultaneously secrete a bispecific innate immune cell engager (BiCE) targeting both GD2 and CD16a. In vitro, GPC2.CAR-GD2.BiCE T-cells induce GPC2-dependent cytotoxicity and secrete GD2.BiCE that promotes GD2-dependent activation of antitumor innate immunity. In vivo, GPC2.CAR-GD2.BiCE T-cells locally deliver GD2.BiCE and increase intratumor retention of NK-cells. In mice bearing neuroblastoma patient-derived xenografts and reconstituted with human CD16a-expressing immune cells, GD2.BiCEs enhance GPC2.CAR antitumor efficacy. A CAR.BiCE strategy should be considered for tumor histologies where antigen escape limits CAR efficacy, especially for solid tumors like neuroblastoma that are infiltrated by innate immune cells
