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Awad, Mohamed E.

https://orcid.org/0000-0001-7525-5364

Mayo Clinic

Western University of Health Sciences

Citations 3

Author response: O-GlcNAc glycosylation orchestrates fate decision and niche function of bone marrow stromal progenitors
Zhang, Zengdi , Awad, Mohamed E. , Elsalanty, Mohammed , Maynard, Jason C. , Burlingame, Alma L. , Huang, Zan , Cray, James , Ball, Lauren Elizabeth , Zeng, Hu , Mansky, Kim C. , Ruan, Hai‐Bin

No container title available | March 22, 2023 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.7554/elife.85464.sa2 Get It

O-GlcNAc glycosylation orchestrates fate decision and niche function of bone marrow stromal progenitors
Zhang, Zengdi , Awad, Mohamed E. , Elsalanty, Mohammed , Cray, James , Maynard, Jason C. , Burlingame, Alma L. , Ruan, Hai‐Bin , Ruan, Hai-Bin , Huang, Zan , Ball, Lauren Elizabeth , Zeng, Hu , Mansky, Kim C.

eLife | March 2, 2023 | Volume: 12 | Issue: No issue available | Pages: No page available

10.7554/elife.85464 Get It

In mammals, interactions between the bone marrow (BM) stroma and hematopoietic progenitors contribute to bone-BM homeostasis. Perinatal bone growth and ossification provide a microenvironment for the transition to definitive hematopoiesis; however, mechanisms and interactions orchestrating the development of skeletal and hematopoietic systems remain largely unknown. Here, we establish intracellular O-linked β-N-acetylglucosamine (O-GlcNAc) modification as a posttranslational switch that dictates the differentiation fate and niche function of early BM stromal cells (BMSCs). By modifying and activating RUNX2, O-GlcNAcylation promotes osteogenic differentiation of BMSCs and stromal IL-7 expression to support lymphopoiesis. In contrast, C/EBPβ-dependent marrow adipogenesis and expression of myelopoietic stem cell factor (SCF) is inhibited by O-GlcNAcylation. Ablating O-GlcNAc transferase (OGT) in BMSCs leads to impaired bone formation, increased marrow adiposity, as well as defective B-cell lymphopoiesis and myeloid overproduction in mice. Thus, the balance of osteogenic and adipogenic differentiation of BMSCs is determined by reciprocal O-GlcNAc regulation of transcription factors, which simultaneously shapes the hematopoietic niche.
Meta-Analysis and Evidence Base for the Efficacy of Autologous Bone Marrow Mesenchymal Stem Cells in Knee Cartilage Repair: Methodological Guidelines and Quality Assessment
Awad, Mohamed E. , Abdelsamid, Mohamed Farouk, Aguilar‐Perez, Alexandra, Mohsen, Ibrahim , Hunter, Monte, Hamrick, Mark W. , Isales, Carlos M. , Elsalanty, Mohammed , Hill, William , Fulzele, Sadanand , Elsisy, Mohamed F. , Abdelsamid, Mohamed F, Hamrick, Mark W , Hill, William D , Fulzele, Sadanand , Hussein, Khaled A. , Helwa, Inas

Stem Cells International | April 7, 2019 | Volume: 2019 | Issue: No issue available | Pages: 1-15

10.1155/2019/3826054 Get It

The aim of this study is to review all the published clinical trials on autologous bone marrow mesenchymal stem cells (BM-MSCs) in the repair of cartilage lesions of the knee. We performed a comprehensive search in three electronic databases: PubMed, Medline via Ovid, and Web of Science. A systematic review was conducted according to the guidelines of PRISMA protocol and the Cochrane Handbook for Systematic Reviews of Interventions. The modified Coleman methodology score was used to assess the quality of the included studies. Meta-analysis was conducted to estimate the effect size for Pain and function change after receiving BM-MSCs. Thirty-three studies—including 724 patients of mean age 44.2 years—were eligible. 50.7% of the included patients received cultured BM-MSCs for knee cartilage repair. There was improvement in the MINORS quality score over time with a positive correlation with the publication year. Meta-analysis indicated better improvement and statistical significance in the Visual Analog Scale for Pain, IKDC Function, Tegner Activity Scale, and Lysholm Knee Score after administration of noncultured BM-MSCs when compared to evaluation before the treatment. Meanwhile, there was a clear methodological defect in most studies with an average modified Coleman methodology score (MCMS) of 55. BM-MSCs revealed a clinically relevant improvement in pain, function, and histological regeneration.