Thai, Victoria L Candelas, Diego O Leach, J Kent
Mesenchymal stromal cells (MSCs) are under investigation for wound healing and tissue regeneration due to their potent secretome. Compared to monodisperse cells, MSC spheroids exhibit increased cell survival and enhanced secretion of endogenous factors such as vascular endothelial growth factor (VEGF) and prostaglandin E2 (PGE2), two key factors in...
Xue, Dixuan Lu, Shan Zhang, Hailing Zhang, Li Dai, Zhijun Kaufman, Dan S Zhang, Jin
T cells, natural killer (NK) cells, macrophages (Macs), and dendritic cells (DCs) are among the most common sources for immune-cell-based therapies for cancer. Antitumor activity can be enhanced in induced pluripotent stem cell (iPSC)-derived immune cells by using iPSCs as a platform for stable genetic modifications that impact immuno-activating or...
Dagar, Gunjan Gupta, Ashna Masoodi, Tariq Nisar, Sabah Merhi, Maysolun Hashem, Sheema Chauhan, Ravi Dagar, Manisha Mirza, Sameer Bagga, Puneet
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Traditional cancer treatments use nonspecific drugs and monoclonal antibodies to target tumor cells. Chimeric antigen receptor (CAR)-T cell therapy, however, leverages the immune system's T-cells to recognize and attack tumor cells. T-cells are isolated from patients and modified to target tumor-associated antigens. CAR-T therapy has achieved FDA a...
Stelmach, Patrick Richter, Sarah Sauer, Sandra Fabre, Margarete A Gu, Muxin Rohde, Christian Janssen, Maike Liebers, Nora Proynova, Rumyana Weinhold, Niels
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Clonal hematopoiesis (CH) is an age-related condition driven by stem- and progenitor cells harboring recurrent mutations linked to myeloid neoplasms. Currently, potential effects on hematopoiesis, stem cell function and regenerative potential under stress conditions are unknown. We performed targeted DNA sequencing of 457 hematopoietic stem cell gr...
Wang, Bohan Gao, Wenjun Zheng, Micha Y Lin, Guiting Lue, Tom F
IntroductionWhile phosphodiesterase type 5 inhibitors (PDE5is) and others are used to treat Erectile dysfunction (ED), many patients are either unresponsive or resistant to it. Stem cell therapy (SCT) is a promising alternative approach. Numerous preclinical trials have demonstrated improved erectile function in animal models using SCT, although th...
Xu, Xiao Xia, Tian
The success of mRNA vaccines during the COVID-19 pandemic has greatly accelerated the development of mRNA therapy. mRNA is a negatively charged nucleic acid that serves as a template for protein synthesis in the ribosome. Despite its utility, the instability of mRNA requires suitable carriers for in vivo delivery. Lipid nanoparticles (LNPs) are emp...
Lu, Ting-Yu Xiang, Yi Tang, Min Chen, Shaochen
Purpose of reviewBioengineering of functional cardiac tissue composed of primary cardiomyocytes has great potential for myocardial regeneration and in vitro tissue modeling. 3D bioprinting was developed to create cardiac tissue in hydrogels that can mimic the structural, physiological, and functional features of native myocardium. Through a detaile...
Yale, Andrew R Kim, Estelle Gutierrez, Brenda Hanamoto, J Nicole Lav, Nicole S Nourse, Jamison L Salvatus, Marc Hunt, Robert F Monuki, Edwin S Flanagan, Lisa A
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Undifferentiated neural stem and progenitor cells (NSPCs) encounter extracellular signals that bind plasma membrane proteins and influence differentiation. Membrane proteins are regulated by N-linked glycosylation, making it possible that glycosylation plays a critical role in cell differentiation. We assessed enzymes that control N-glycosylation i...
Hu, Xiaomeng White, Kathy Olroyd, Ari G DeJesus, Rowena Dominguez, Antonia A Dowdle, William E Friera, Annabelle M Young, Chi Wells, Frank Chu, Elaine Y
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Genetic engineering of allogeneic cell therapeutics that fully prevents rejection by a recipient's immune system would abolish the requirement for immunosuppressive drugs or encapsulation and support large-scale manufacturing of off-the-shelf cell products. Previously, we generated mouse and human hypoimmune pluripotent (HIP) stem cells by depletin...
Chamberlain, Jeffrey S Robb, Melissa Braun, Serge Brown, Kristy J Danos, Olivier Ganot, Annie Gonzalez-Alegre, Pedro Hunter, Nina McDonald, Craig Morris, Carl
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Duchenne muscular dystrophy (DMD) is a serious, rare genetic disease, affecting primarily boys. It is caused by mutations in the DMD gene and is characterized by progressive muscle degeneration that results in loss of function and early death due to respiratory and/or cardiac failure. Although limited treatment options are available, some for only ...