Dr. Arshad Ayyaz

Assistant Professor,

Department of Biological Sciences, Faculty of Science, University of Calgary, 2500 University Dr NW, Calgary, AB T2N 1N4, Canada

arshad.ayyaz@ucalgary.ca

Dr. Ayyaz is a distinguished geneticist and stem cell biologist, renowned for his seminal contributions to the fields of somatic tissue repair, inflammation, fibrosis, and oncology. His pioneering research has significantly augmented our comprehension of the intricate mechanisms governing somatic stem cell regulation under physiological conditions and the aberrations that manifest in pathological states.

In a groundbreaking study published in Nature Cell Biology in 2015, Dr. Ayyaz elucidated the role of innate immune cells in modulating stem cell activity through the invocation of conserved developmental pathways. This seminal work revealed a dual role for these pathways: promoting regeneration of the intestinal epithelium on one hand, and stimulating tumorigenic proliferation of stem cell clusters on the other (Ayyaz et al., 2015, Nature Cell Biology).

Subsequently, Dr. Ayyaz spearheaded a single-cell genomics study that led to the identification and characterization of a novel stem cell type, which he aptly termed the "revival stem cell." His findings underscored the quintessential role these cells play in facilitating the regeneration of the intestinal epithelium post-injury and in the aftermath of homeostatic stem cell ablation in the intestine (Ayyaz et al., 2019, Nature).

Beyond these accomplishments, Dr. Ayyaz has been an active collaborator with various research teams, both within Canada and internationally. His collaborative endeavors have been instrumental in unveiling the molecular signaling pathways that facilitate stem cell interactions with their microenvironment in health and disease, encompassing elements such as the mesenchyme, immune system, gut microbiota, and enteric pathogens (e.g., Dervovic et al., 2023 in Nature Communications; Baghdadi et al., 2021 in Cell Stem Cell; Goldsmith et al., 2020 in Nature Communications; Sousa-Victor et al., 2017 in Cell Reports).