Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Aug 4:13:952071.
doi: 10.3389/fimmu.2022.952071. eCollection 2022.

Mesenchymal stem/stromal cells in the pathogenesis and regenerative therapy of inflammatory bowel diseases

Affiliations
Review

Mesenchymal stem/stromal cells in the pathogenesis and regenerative therapy of inflammatory bowel diseases

Zhengping Che et al. Front Immunol. .

Abstract

Inflammatory bowel diseases (IBDs) represent a group of chronic inflammatory disorders of the gastrointestinal (GI) tract including ulcerative colitis (UC), Crohn's disease (CD), and unclassified IBDs. The pathogenesis of IBDs is related to genetic susceptibility, environmental factors, and dysbiosis that can lead to the dysfunction of immune responses and dysregulated homeostasis of local mucosal tissues characterized by severe inflammatory responses and tissue damage in GI tract. To date, extensive studies have indicated that IBDs cannot be completely cured and easy to relapse, thus prompting researchers to find novel and more effective therapeutics for this disease. Due to their potent multipotent differentiation and immunomodulatory capabilities, mesenchymal stem/stromal cells (MSCs) not only play an important role in regulating immune and tissue homeostasis but also display potent therapeutic effects on various inflammatory diseases, including IBDs, in both preclinical and clinical studies. In this review, we present a comprehensive overview on the pathological mechanisms, the currently available therapeutics, particularly, the potential application of MSCs-based regenerative therapy for IBDs.

Keywords: Crohn’s disease; inflammatory bowel diseases; mesenchymal stem/stromal cells; regenerative therapy; ulcerative colitis.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
(A) The self-renewal and multipotent differentiation functions of MSCs. (B) The mechanism of immune responses in the pathogenic process of IBDs.
Figure 2
Figure 2
Schematic diagram of the mechanism of MSCs treatment in IBDs. (A) The secretion of anti-proliferative soluble factors. (B) Cell-To-Cell Contact. (C) Exosomes treatment. (D) Mitochondria transfer. (E) MSCs express PD-L1.

References

    1. Fujino S, Andoh A, Bamba S, Ogawa A, Hata K, Araki Y, et al. . Increased expression of interleukin 17 in inflammatory bowel disease. Gut (2003) 52:65–70. doi: 10.1136/gut.52.1.65 - DOI - PMC - PubMed
    1. Rogler G, Vavricka S. Exposome in ibd: Recent insights in environmental factors that influence the onset and course of ibd. Inflammation Bowel Dis (2015) 21:400–8. doi: 10.1097/MIB.0000000000000229 - DOI - PubMed
    1. Abraham BP. Symptom management in inflammatory bowel disease. Expert Rev Gastroenterol Hepatol (2015) 9:953–67. doi: 10.1586/17474124.2015.1038241 - DOI - PubMed
    1. Nowakowski J, Chrobak AA, Dudek D. Psychiatric illnesses in inflammatory bowel diseases - psychiatric comorbidity and biological underpinnings. Psychiatr Pol (2016) 50:1157–66. doi: 10.12740/PP/62382 - DOI - PubMed
    1. Bonaz B, Sinniger V, Pellissier S. Therapeutic potential of vagus nerve stimulation for inflammatory bowel diseases. Front Neurosci (2021) 15:650971. doi: 10.3389/fnins.2021.650971 - DOI - PMC - PubMed

Publication types

MeSH terms