# Dietary Pectin Increases Intestinal Crypt Stem Cell Survival following Radiation Injury

**Authors:** Sripathi M. Sureban, Randal May, Dongfeng Qu, Parthasarathy Chandrakesan, Nathaniel Weygant, Naushad Ali, Stan A. Lightfoot, Kai Ding, Shahid Umar, Michael J. Schlosser, Courtney W. Houchen

PMC · DOI: 10.1371/journal.pone.0135561 · PLoS ONE · 2015-08-13

## TL;DR

Dietary pectin helps protect the intestines from radiation damage by increasing stem cell survival and improving overall survival in mice.

## Contribution

This study demonstrates dietary pectin's novel radioprotective effect on intestinal stem cells and survival post-radiation.

## Key findings

- Pectin treatment increased intestinal crypt stem cell survival three-fold after radiation.
- Pectin improved overall survival in mice exposed to lethal radiation doses.
- Pectin increased expression of key stem cell and survival markers like Dclk1 and Lgr5.

## Abstract

Gastrointestinal (GI) mucosal damage is a devastating adverse effect of radiation therapy. We have recently reported that expression of Dclk1, a Tuft cell and tumor stem cell (TSC) marker, 24h after high dose total-body gamma-IR (TBI) can be used as a surrogate marker for crypt survival. Dietary pectin has been demonstrated to possess chemopreventive properties, whereas its radioprotective property has not been studied. The aim of this study was to determine the effects of dietary pectin on ionizing radiation (IR)-induced intestinal stem cell (ISC) deletion, crypt and overall survival following lethal TBI. C57BL/6 mice received a 6% pectin diet and 0.5% pectin drinking water (pre-IR mice received pectin one week before TBI until death; post-IR mice received pectin after TBI until death). Animals were exposed to TBI (14 Gy) and euthanized at 24 and 84h post-IR to assess ISC deletion and crypt survival respectively. Animals were also subjected to overall survival studies following TBI. In pre-IR treatment group, we observed a three-fold increase in ISC/crypt survival, a two-fold increase in Dclk1+ stem cells, increased overall survival (median 10d vs. 7d), and increased expression of Dclk1, Msi1, Lgr5, Bmi1, and Notch1 (in small intestine) post-TBI in pectin treated mice compared to controls. We also observed increased survival of mice treated with pectin (post-IR) compared to controls. Dietary pectin is a radioprotective agent; prevents IR-induced deletion of potential reserve ISCs; facilitates crypt regeneration; and ultimately promotes overall survival. Given the anti-cancer activity of pectin, our data support a potential role for dietary pectin as an agent that can be administered to patients receiving radiation therapy to protect against radiation-induces mucositis.

## Linked entities

- **Genes:** DCLK1 (doublecortin like kinase 1) [NCBI Gene 9201], MSI1 (musashi RNA binding protein 1) [NCBI Gene 4440], LGR5 (leucine rich repeat containing G protein-coupled receptor 5) [NCBI Gene 8549], BMI1 (BMI1 proto-oncogene, polycomb ring finger) [NCBI Gene 648], NOTCH1 (notch receptor 1) [NCBI Gene 4851]
- **Chemicals:** pectin (PubChem CID 441476)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Notch1 (notch 1) [NCBI Gene 18128] {aka 9930111A19Rik, Mis6, N1, Tan1, lin-12}, Bmi1 (Bmi1 proto-oncogene, polycomb ring finger) [NCBI Gene 12151] {aka Bmi-1, Pcgf4}, Dclk1 (doublecortin-like kinase 1) [NCBI Gene 13175] {aka 1700113D08Rik, 2810480F11Rik, Click-I, Cpg16, Dcamkl1, Dcl}, Lgr5 (leucine rich repeat containing G protein coupled receptor 5) [NCBI Gene 14160] {aka FEX, Gpr49}, Msi1 (musashi RNA-binding protein 1) [NCBI Gene 17690] {aka Msi1h, Musahi1, m-Msi-1}, CLDN7 (claudin 7) [NCBI Gene 1366] {aka CEPTRL2, CLDN-7, CPETRL2, Hs.84359, claudin-1}, TJP1 (tight junction protein 1) [NCBI Gene 7082] {aka ZO-1}, TJP2 (tight junction protein 2) [NCBI Gene 9414] {aka C9DUPq21.11, DFNA51, DUP9q21.11, FHCA1, PFIC4, X104}, Dntt (deoxynucleotidyltransferase, terminal) [NCBI Gene 21673] {aka Tdt}, Cdkn1a (cyclin dependent kinase inhibitor 1A) [NCBI Gene 12575] {aka CAP20, CDKI, CIP1, Cdkn1, P21, SDI1}, DCLK1 (doublecortin like kinase 1) [NCBI Gene 9201] {aka CL1, CLICK1, DCAMKL1, DCDC3A, DCLK}, CLDN1 (claudin 1) [NCBI Gene 9076] {aka CLD1, ILVASC, SEMP1}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}
- **Diseases:** pain (MESH:D010146), hyperplasia (MESH:D006965), ISC (MESH:C567703), rectal bleeding (MESH:D012002), inflammation (MESH:D007249), constipation (MESH:D003248), cervical dislocation (MESH:D002575), colon tumors (MESH:D003110), malabsorption syndromes (MESH:D008286), gut mucosal damage (MESH:D052016), bacterial infection (MESH:D001424), imbalances (MESH:D000137), cancer (MESH:D009369), loss (MESH:D016388), mucosal ulceration (MESH:D014456), IR (MESH:D011832), Gastrointestinal (GI) mucosal damage (MESH:D005767), diarrhea (MESH:D003967), infection (MESH:D007239), lethargic (MESH:D004674), damage (MESH:D020263), injury to ISCs (MESH:D014947), nausea and vomiting (MESH:D020250), abdominal and pelvic tumors (MESH:D000008), Death (MESH:D003643), toxicity (MESH:D064420), hypotension (MESH:D007022), acute radiation injury (MESH:D054508), TBI (MESH:D006362),  (MESH:D011833)
- **Chemicals:** amino-acid (MESH:D000596), paraffin (MESH:D010232), polysaccharide (MESH:D011134), thiol (MESH:D013438), thiophosphate (MESH:C035638), cellulose (MESH:D002482), dUTP (MESH:C027078), galactoside (MESH:D005697), Amifostine (MESH:D004999), Androstenediol (MESH:D015114), citrate (MESH:D019343), hydrogen peroxide (MESH:D006861), hemicellulose (MESH:C007916), 5-bromo-2'-deoxyuridine (MESH:D001973), CO2 (MESH:D002245), cysteine (MESH:D003545), Pectin (MESH:D010368), citrus pectin (MESH:C586814), BrdUrd (-), formalin (MESH:D005557), PBS (MESH:D007854), 137Cs (MESH:C000614989), water (MESH:D014867),  (MESH:D011837)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU)

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC4536042/full.md

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Source: https://tomesphere.com/paper/PMC4536042