Enhancement of Murine Intestinal Stem Cell Survival after Irradiation by Keratinocyte Growth Factor

1997 ◽  
Vol 148 (3) ◽  
pp. 248 ◽  
Author(s):  
Waqqar B. Khan ◽  
Chaoxiang Shui ◽  
Shoucheng Ning ◽  
Susan J. Knox
2019 ◽  
Vol 12 ◽  
pp. 117906601983696 ◽  
Author(s):  
Elle Koren ◽  
Yaron Fuchs

Although much is known regarding intestinal stem cell (ISC) self-renewal and differentiation, the specific mechanisms used for their elimination is unclear. We recently discovered that the pro-apoptotic protein ARTS, a Septin4 isoform, interacts with X-linked inhibitor of apoptosis (XIAP) in the ISC niche to regulate stem cell survival during intestinal homeostasis and regeneration. These findings point to an intriguing avenue of translational research, examining how manipulation of stem cell apoptosis through the ARTS/XIAP module can affect stem-cell-dependent processes.


RSC Advances ◽  
2015 ◽  
Vol 5 (69) ◽  
pp. 55948-55956 ◽  
Author(s):  
Young Min Shin ◽  
Jong-Young Lim ◽  
Jong-Seok Park ◽  
Hui-Jeong Gwon ◽  
Sung In Jeong ◽  
...  

Co-immobilization of EGF and gelatin on a fibrous mesh promotes spreading and viability of hMSC, and coupled EGF involves involucrin expression and procollagen secretion, indicating trans-differentiation to keratinocyte-like cell.


2021 ◽  
Author(s):  
Wesley Tung ◽  
Ullas Valiya Chembazhi ◽  
Jing Yang ◽  
Ka Lam Nguyen ◽  
Aryan Lalwani ◽  
...  

Properly controlled intestinal epithelial cell regeneration is not only vital for protection against insults from environmental hazards but also crucial for preventing intestinal cancer. Intestinal stem cells located in the crypt region provide the driving force for epithelial regeneration, and thus their survival and death must be precisely regulated. We show here that polypyrimidine tract binding protein 1 (PTBP1, also called heterogeneous nuclear ribonucleoprotein I, or HNRNP I), an RNA-binding protein that post-transcriptionally regulates gene expression, is critical for intestinal stem cell survival and stemness. Mechanistically, we show that PTBP1 inhibits the expression of PHLDA3, an AKT repressor, and thereby maintains AKT activity in the intestinal stem cell compartment to promote stem cell survival and proliferation. Furthermore, we show that PTBP1 inhibits the expression of PTBP2, a paralog of PTBP1 that is known to induce neuron differentiation, through repressing inclusion of alternative exon 10 to Ptbp2 transcript. Loss of PTBP1 results in a significant upregulation of PTBP2, which is accompanied by splicing changes in genes that are important for neuron cell development. This finding suggests that PTBP1 prevents aberrant differentiation of intestinal stem cells into neuronal cells through inhibiting PTBP2. Our results thus reveal a novel mechanism whereby PTBP1 maintains intestinal stem cell survival and stemness through the control of gene function post-transcriptionally.


2009 ◽  
Vol 296 (2) ◽  
pp. G245-G254 ◽  
Author(s):  
Robert J. George ◽  
Mark A. Sturmoski ◽  
Randal May ◽  
Sripathi M. Sureban ◽  
Brian K. Dieckgraefe ◽  
...  

The microcolony assay following gamma irradiation (IR) is a functional assay of intestinal stem cell fate. The cyclin-dependent kinase (CDK) inhibitor p21Waf1/Cip1/Sdi1(p21) regulates cell cycle arrest following DNA damage. To explore the role of p21 on stem cell fate, we examined the effects of p21 deletion on intestinal crypt survival following IR and expression of the stem/progenitor cell marker Musashi-1 (Msi-1) and the antiapoptotic gene survivin. Intestinal stem cell survival in adult wild-type (WT) and p21−/−mice was measured using the microcolony assay. Msi-1, p21, and survivin mRNA were measured using real-time PCR and immunohistochemical analysis. Laser capture microdissection (LCM) was used to isolate mRNA from the crypt stem cell zone. No differences in radiation-induced apoptosis were observed between WT and p21−/−mice. However, increased crypt survival (3.0-fold) was observed in p21−/−compared with WT mice 3.5 days after 13 Gy. Msi-1 and survivin mRNA were elevated 12- and 7.5-fold, respectively, in LCM-dissected crypts of p21−/−compared with WT mice. In conclusion, deletion of p21 results in protection of crypt stem/progenitor cells from IR-induced cell death. Furthermore, the increase in crypt survival is associated with increased numbers of Msi-1- and survivin-expressing cells in regenerative crypts.


Blood ◽  
2017 ◽  
Vol 129 (3) ◽  
pp. 307-318 ◽  
Author(s):  
David J. H. F. Knapp ◽  
Colin A. Hammond ◽  
Nima Aghaeepour ◽  
Paul H. Miller ◽  
Davide Pellacani ◽  
...  

Key Points Human HSCs show higher tonic signaling activity in multiple pathways than MPPs. Growth factor–activated AKT and β-catenin in human HSCs regulate their survival and mitogenesis.


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