Benson M. George

ORCID: 0000-0003-4031-0954
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About
Contact & Profiles
Research Areas
  • Single-cell and spatial transcriptomics
  • Hematopoietic Stem Cell Transplantation
  • Immune Cell Function and Interaction
  • CAR-T cell therapy research
  • RNA modifications and cancer
  • Immune cells in cancer
  • RNA and protein synthesis mechanisms
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Glycosylation and Glycoproteins Research
  • Acute Myeloid Leukemia Research
  • Neurogenesis and neuroplasticity mechanisms
  • Immunotherapy and Immune Responses
  • T-cell and B-cell Immunology
  • Phagocytosis and Immune Regulation
  • Epigenetics and DNA Methylation
  • Nausea and vomiting management
  • Anesthesia and Pain Management
  • Spine and Intervertebral Disc Pathology
  • Cell Image Analysis Techniques
  • Bone health and osteoporosis research
  • Erythrocyte Function and Pathophysiology
  • Dental Anxiety and Anesthesia Techniques
  • Monoclonal and Polyclonal Antibodies Research
  • Pluripotent Stem Cells Research
  • Chromosomal and Genetic Variations

Dana-Farber Cancer Institute
2024-2025

Boston Children's Hospital
2023-2025

Boston Children's Museum
2025

Harvard University
2023-2024

Stanford University
2015-2023

Brigham and Women's Hospital
2022-2023

Boston University
2023

California Institute for Regenerative Medicine
2016-2022

Institute for Stem Cell Biology and Regenerative Medicine
2019-2020

Maimonides Medical Center
2016-2019

Nicole Almanzar Jane Antony Ankit S. Baghel Isaac Bakerman Ishita Bansal and 95 more Ben A. Barres Philip A. Beachy Daniela Berdnik Biter Bilen Douglas Brownfield Corey J. Cain Charles K. F. Chan Michelle B. Chen Michael F. Clarke Stephanie D. Conley Spyros Darmanis Aaron Demers Kubilay Demir Antoine de Morrée Tessa Divita Haley du Bois Hamid Ebadi F. Hernán Espinoza Matt Fish Qiang Gan Benson M. George Astrid Gillich Rafael Gómez-Sjöberg Foad Green Geraldine Genetiano Xueying Gu Gunsagar S. Gulati Oliver Hãhn Michael S. Haney Yan Hang Lincoln Harris Mu He Shayan Hosseinzadeh Albin Huang Kerwyn Casey Huang Tal Iram Taichi Isobe Feather Ives Robert C. Jones Kevin S. Kao Jim Karkanias Guruswamy Karnam Andreas Keller Aaron M. Kershner Nathalie Khoury Seung K. Kim Bernhard Kiss William Kong Mark A. Krasnow Maya E. Kumar Christin S. Kuo Jonathan Y. Lam Davis P. Lee Song Eun Lee Benoit Lehallier Olivia Leventhal Guang Li Qingyun Li Ling Liu Annie Lo Wan-Jin Lu Maria Lugo-Fagundo Anoop Manjunath Andrew P. May Ashley Maynard Aaron McGeever Marina McKay M. Windy McNerney Bryan D. Merrill Ross J. Metzger Marco Mignardi Dullei Min Ahmad N. Nabhan Norma Neff Katharine M. Ng Patricia K. Nguyen Joseph J. Noh Roel Nusse Róbert Pálovics Rasika Patkar Weng Chuan Peng Lolita Penland Angela Oliveira Pisco Katherine S. Pollard Robert Puccinelli Zhen Qi Stephen R. Quake Thomas A. Rando Eric Rulifson Nicholas Schaum Joe M. Segal Shaheen S. Sikandar Rahul Sinha Rene Sit Justin L. Sonnenburg

10.1038/s41586-020-2496-1 article EN Nature 2020-07-15

To define the cellular composition and architecture of cutaneous squamous cell carcinoma (cSCC), we combined single-cell RNA sequencing with spatial transcriptomics multiplexed ion beam imaging from a series human cSCCs matched normal skin. cSCC exhibited four tumor subpopulations, three recapitulating epidermal states, tumor-specific keratinocyte (TSK) population unique to cancer, which localized fibrovascular niche. Integration data mapped ligand-receptor networks specific types, revealing...

10.1016/j.cell.2020.05.039 article EN cc-by Cell 2020-06-23

10.1038/s41586-020-2499-y article EN Nature 2020-07-15

Aneuploidy decreases cellular fitness, yet it is also associated with cancer, a disease of enhanced proliferative capacity. To investigate one mechanism by which aneuploidy could contribute to tumorigenesis, we examined the effects on genomic stability. We analyzed 13 budding yeast strains that carry extra copies single chromosomes and found all aneuploid exhibited or more forms instability. Most displayed increased chromosome loss mitotic recombination, as well defective DNA damage repair....

10.1126/science.1206412 article EN Science 2011-08-18

Interleukin-2 (IL-2) is a cytokine required for effector T cell expansion, survival, and function, especially engineered cells in adoptive immunotherapy, but its pleiotropy leads to simultaneous stimulation suppression of immune responses as well systemic toxicity, limiting therapeutic use. We IL-2 cytokine-receptor orthogonal (ortho) pairs that interact with one another, transmitting native signals, do not their natural receptor counterparts. Introduction orthoIL-2Rβ into enabled the...

10.1126/science.aar3246 article EN Science 2018-03-01

Significance Cancer immunotherapy is a promising therapeutic intervention. However, complete and durable responses are only seen in fraction of patients who have cancer. Although cells the myeloid lineage frequently infiltrate tumors limit success, currently approved immunotherapies primarily target tumor-infiltrating T natural killer lymphocytes. The inhibitory receptor signal regulatory protein-α (SIRPα) represents myeloid-specific immune checkpoint that engages “don’t eat me” CD47. Here,...

10.1073/pnas.1710877114 article EN Proceedings of the National Academy of Sciences 2017-11-20

10.1038/s41586-022-04461-2 article EN Nature 2022-03-02

Abstract The diversity of cell types is a challenge for quantifying aging and its reversal. Here we develop ‘aging clocks’ based on single-cell transcriptomics to characterize cell-type-specific rejuvenation. We generated transcriptomes from the subventricular zone neurogenic region 28 mice, tiling ages young old. trained single-cell-based regression models predict chronological age biological (neural stem proliferation capacity). These clocks are generalizable independent cohorts other...

10.1038/s43587-022-00335-4 article EN cc-by Nature Aging 2022-12-19

Targeted protein degradation is an emerging strategy for the elimination of classically undruggable proteins. Here, to expand landscape targetable substrates, we designed degraders that achieve substrate selectivity via recognition a discrete peptide and glycan motif cell-type antigen-driven cell-surface binding. We applied this approach mucins, O-glycosylated proteins drive cancer progression through biophysical immunological mechanisms. Engineering bacterial mucin-selective protease...

10.1038/s41587-023-01840-6 article EN cc-by Nature Biotechnology 2023-08-03

Significance This is the first in-depth profiling of pancreatic neuroendocrine tumors (PanNETs), to our knowledge, that illuminates fundamental biological processes for this class tumors. Beginning with index case and confirmed additional patient tumors, we showed dependence on paracrine signaling through hepatocyte growth factor (HGF)/receptor tyrosine kinase MET axis. We created a novel cell line derived from well-differentiated PanNET autocrine HGF/MET signaling. also identified...

10.1073/pnas.1600007113 article EN Proceedings of the National Academy of Sciences 2016-03-31

Glycans modify protein, lipid, and even RNA molecules to form the regulatory outer coat on cells called glycocalyx. The changes in glycosylation have been linked initiation progression of many diseases. Thus, while significance is well established, a lack accessible methods characterize glycans has hindered ability understand their biological functions. Mass spectrometry (MS)-based generally at core most glycan profiling efforts; however, modern data-independent acquisition (DIA), which...

10.1101/2024.03.12.584702 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-03-13

The balance of hematopoietic stem cell (HSC) self-renewal and differentiation is critical for a healthy blood supply; imbalances underlie hematological diseases. importance HSCs their progenitors have led to extensive characterization at genomic transcriptomic levels. However, the proteomics hematopoiesis remains incompletely understood. Here we report resource from mass spectrometry mouse young adult old HSCs, multipotent oligopotent progenitors; 12 types in total. We validated differential...

10.7554/elife.62210 article EN cc-by eLife 2020-11-25

The Tabula Muris Consortium We have created a compendium of single cell transcriptome data from the model organism Mus musculus comprising more than 100,000 cells 20 organs and tissues. These represent new resource for biology, revealing gene expression in poorly characterized populations allowing direct controlled comparison types shared between tissues, such as T-lymphocytes endothelial distinct anatomical locations. Two technical approaches were used most tissues: one approach,...

10.1101/237446 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2017-12-20

Key Points Upon injury, the mesothelium recruits neutrophils to peritoneal space, which contributes adhesion formation. Neutrophil recruitment and macrophage-depletion kinetics in adhesions differ from normal innate response.

10.1182/bloodadvances.2018024026 article EN cc-by-nc-nd Blood Advances 2019-09-13

Abstract Chemical tools enable precise characterization of many biopolymers, including glycoconjugates. Metabolic chemical reporters enabled the discovery glycoRNAs, however they have certain limitations due requirement having living cells to incorporate modified sugar. Here we develop a periodate oxidation and aldehyde ligation method detect characterize native sialoglycoRNAs, termed rPAL. With optimized RNA biochemistry enhance recovery analysis small RNAs, show rPAL is at least an order...

10.1101/2023.02.26.530106 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2023-02-26
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