A photo of Matthew Kofron.

J. Matthew Kofron, PhD


  • Director, Bio-Imaging and Analysis Facility
  • Professor, UC Department of Pediatrics

About

Biography

I chose to become a researcher because of my passion for discovery and innovation. My research interests include developmental biology, germ layer formation, cell signaling, microscopy, immunology, lung biology and digestive disease. I began my work at Cincinnati Children’s in 2000 and have more than 30 years of research experience. I received the Senior Faculty Service award in 2020 from Cincinnati Children’s.

In my early career, I focused on embryonic development and cell-cell signaling. I now facilitate the use of microscopy and advanced imaging for other researchers in the Cincinnati Children’s Research Foundation in the Bio-Imaging and Analysis Facility. This type of advanced imaging provides a high resolution that allows microscopic visualization down to the subcellular level. In addition to imaging, we have developed tools for analysis and methodologies for image interpretation for quantitative analysis.

My work has been published in various publications, including Nature, Cell Stem Cell, Developmental Cell, Nature Cell Biology, Clinical Cytometry, Genes and Brain Behavior and Hepatology.

PhD: University of Minnesota, Minneapolis, MN, 1999.

Interests

Early vertebrate patterning; germ layer formation

Research Areas

Developmental Biology, Fibrosis

Publications

Single-cell sequencing dissects the transcriptional identity of activated fibroblasts and identifies novel persistent distal tubular injury patterns in kidney fibrosis. Rudman-Melnick, V; Adam, M; Stowers, K; Potter, A; Ma, Q; Chokshi, SM; Vanhoutte, D; Valiente-Alandi, I; Lindquist, DM; Nieman, ML; Kofron, JM; Chung, E; Park, JS; Potter, SS; Devarajan, P. Scientific Reports. 2024; 14:439.

Resilient anatomy and local plasticity of naive and stress haematopoiesis. Wu, Q; Zhang, J; Kumar, S; Shen, S; Kincaid, M; Johnson, CB; Zhang, YS; Turcotte, R; Alt, C; Ito, K; Ito, K; Way, SS; Kofron, JM; Lucas, D. Nature. 2024; 627:839-846.

Alveolar epithelial progenitor cells require Nkx2-1 to maintain progenitor-specific epigenomic state during lung homeostasis and regeneration. Toth, A; Kannan, P; Snowball, J; Kofron, M; Wayman, JA; Bridges, JP; Miraldi, ER; Swarr, D; Zacharias, WJ. Nature Communications. 2023; 14:8452.

Single cell transcriptomic analysis of HPV16-infected epithelium identifies a keratinocyte subpopulation implicated in cancer. Bedard, MC; Chihanga, T; Carlile, A; Jackson, R; Brusadelli, MG; Lee, D; VonHandorf, A; Rochman, M; Dexheimer, PJ; Chalmers, J; Lambert, PF; Adam, M; Steven Potter, S; Wells, SI. Nature Communications. 2023; 14:1975.

Pulmonary Alveolar Microlithiasis. Lampl, CD; Wikenheiser-Brokamp, KA; Woods, JC; Matthew Kofron, J; McCormack, FX. Orphan Lung Diseases. : Springer Nature; Springer Nature; 2023.

Rap1b-loss increases neutrophil lactate dehydrogenase activity to enhance neutrophil migration and acute inflammation in vivo. Chowdhury, CS; Wareham, E; Xu, J; Kumar, S; Kofron, M; Lakshmikanthan, S; Chrzanowska, M; Filippi, MD. Frontiers in Immunology. 2022; 13:1061544.

In situ mapping identifies distinct vascular niches for myelopoiesis. Zhang, J; Wu, Q; Johnson, CB; Pham, G; Kinder, JM; Olsson, A; Slaughter, A; May, M; Weinhaus, B; D’Alessandro, A; Way, SS; Salomonis, N; Grimes, HL; Lucas, D. Nature. 2021; 590:457-462.

Patient-Derived Organotypic Epithelial Rafts Model Phenotypes in Juvenile-Onset Recurrent Respiratory Papillomatosis. Bedard, MC; Brusadelli, MG; Carlile, A; Ruiz-Torres, S; Lodin, H; Lee, D; Kofron, M; Lambert, PF; Lane, A; Ameziane, N; Bahassi, EM; Wikenheiser-Brokamp, KA; de Alarcon, A; Smith, DF; Wells, SI. Viruses-Basel. 2021; 13:68.

Single-Cell Profiling of AKI in a Murine Model Reveals Novel Transcriptional Signatures, Profibrotic Phenotype, and Epithelial-to-Stromal Crosstalk. Rudman-Melnick, V; Adam, M; Potter, A; Chokshi, SM; Ma, Q; Drake, KA; Schuh, MP; Matthew Kofron, J; Devarajan, P; Steven Potter, S. Journal of the American Society of Nephrology : JASN. 2020; 31:2793-2814.

Lipopolysaccharide Reverses Hepatic Stellate Cell Activation Through Modulation of cMyb, Small Mothers Against Decapentaplegic, and CCAAT/Enhancer-Binding Protein C/EBP Transcription Factors. Sharma, A; Verma, AK; Kofron, M; Kudira, R; Miethke, A; Wu, T; Wang, J; Gandhi, CR. Hepatology. 2020; 72:1800-1818.

From the Blog

Of Mice and Molecules: Our Confocal Imaging Core
Imaging Sciences

Of Mice and Molecules: Our Confocal Imaging Core

J. Matthew Kofron, PhD6/30/2019