Ankita Singh
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Ankita Singh has a total of 17 co-authors. Here are the top co-authors by number of shared publications:
- Amita Aggarwal
Department of Clinical Immunology and Rheumatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
1 shared publication - Bodduluri Haribabu
Department of Microbiology and Immunology, University of Louisville, Louisville, KY 40202, USA
1 shared publication - Gerald Wayne Dryden
Department of Medicine, University of Louisville, Louisville, USA
1 shared publication - Harikrishnan Gangadharan
Department of Rheumatology, Government Medical College Kottayam, Gandhinagar, India
1 shared publication Khaliqur Rahman
Department of Hematology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India
1 shared publicationKomal Singh
Department of Clinical Immunology and Rheumatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India
1 shared publication
Latest Publications
- Open Access
- 23 June 2026
- Published by Springer Nature in Nature Communications
- Vol. 17 (1) , 5411
Urolithin A activates aryl hydrocarbon receptor-NLRP6-mediated pathways in intestinal epithelial cells to modulate mucosal immunity and strengthen gut barrier integrity
The aryl hydrocarbon receptor (AHR) plays a central role in orchestrating gut barrier and mucosal immune functions in the pathogenesis of inflammatory bowel disease (IBD). Nevertheless, activation of the AHR by diverse ligands yields varied outcomes, and the downstream pathways responsible for these effects remain unknown. Here, we report that selective activation of AHR in mouse intestinal epithelial cells (IEC) by the microbial metabolite, urolithin A (UroA), triggers the Nod-like receptor pyrin domain-containing protein 6 (NLRP6) inflammasome, resulting in the release of interleukin (IL)−18 but not IL-1β. Further, we show that UroA-induced IL-18 in IECs is critical for IL-22, mucin 2 and REG3γ production, as well as protection against colitis. Moreover, UroA significantly upregulates IL-18 and IL-22 levels in IECs and type-3 innate lymphoid cells, respectively, in intestinal biopsies from patients with IBD patients. These results demonstrate that activation of AHR by UroA modulates intestinal barrier function through an NLRP6-IL-18-IL-22 pathway in both healthy and IBD conditions.
- 23 June 2026
- Published by Springer Nature in Nature Communications
- Vol. 17 (1) , 5411
Open AccessUrolithin A activates aryl hydrocarbon receptor-NLRP6-mediated pathways in intestinal epithelial cells to modulate mucosal immunity and strengthen gut barrier integrity
The aryl hydrocarbon receptor (AHR) plays a central role in orchestrating gut barrier and mucosal immune functions in the pathogenesis of inflammatory bowel disease (IBD). Nevertheless, activation of the AHR by diverse ligands yields varied outcomes, and the downstream pathways responsible for these effects remain unknown. Here, we report that selective activation of AHR in mouse intestinal epithelial cells (IEC) by the microbial metabolite, urolithin A (UroA), triggers the Nod-like receptor pyrin domain-containing protein 6 (NLRP6) inflammasome, resulting in the release of interleukin (IL)−18 but not IL-1β. Further, we show that UroA-induced IL-18 in IECs is critical for IL-22, mucin 2 and REG3γ production, as well as protection against colitis. Moreover, UroA significantly upregulates IL-18 and IL-22 levels in IECs and type-3 innate lymphoid cells, respectively, in intestinal biopsies from patients with IBD patients. These results demonstrate that activation of AHR by UroA modulates intestinal barrier function through an NLRP6-IL-18-IL-22 pathway in both healthy and IBD conditions.
- 12 November 2020
- Published by Springer Nature in Indian Journal of Hematology and Blood Transfusion
- Vol. 37 (3) , 511-513
A Rare Cause of Double Negative αβ T Cell Lymphocytosis
- 12 November 2020
- Published by Springer Nature in Indian Journal of Hematology and Blood Transfusion
- Vol. 37 (3) , 511-513
A Rare Cause of Double Negative αβ T Cell Lymphocytosis