Hematopoietic stem and progenitor cells integrate microbial signals to promote post-inflammation gut tissue repair.
Maiko SezakiYoshikazu HayashiGaku NakatoYuxin WangSayuri NakataSubinoy BiswasTatsuya MorishimaMd FakruddinJieun MoonSoyeon AhnPilhan KimYuji MiyamotoHideo BabaShinji FukudaHitoshi TakizawaPublished in: The EMBO journal (2022)
Bone marrow (BM)-resident hematopoietic stem and progenitor cells (HSPCs) are often activated following bacterial insults to replenish the host hemato-immune system, but how they integrate the associated tissue damage signals to initiate distal tissue repair is largely unknown. Here, we show that acute gut inflammation expands HSPCs in the BM and directs them to inflamed mesenteric lymph nodes through GM-CSFR activation for further expansion and potential differentiation into Ly6C + /G + myeloid cells specialized in gut tissue repair. We identified this process to be mediated by Bacteroides, a commensal gram-negative bacteria that activates innate immune signaling. These findings establish cross-organ communication between the BM and distant inflamed sites, whereby a certain subset of multipotent progenitors is specified to respond to imminent hematopoietic demands and to alleviate inflammatory symptoms.
Keyphrases
- bone marrow
- oxidative stress
- lymph node
- innate immune
- induced apoptosis
- mesenchymal stem cells
- liver failure
- microbial community
- immune response
- cell proliferation
- early stage
- minimally invasive
- acute myeloid leukemia
- hepatitis b virus
- cell death
- respiratory failure
- signaling pathway
- neoadjuvant chemotherapy
- climate change
- extracorporeal membrane oxygenation
- sentinel lymph node
- emergency medicine
- sleep quality
- mechanical ventilation