Cell Adhesion Molecule CD166/ALCAM Functions Within the Crypt to Orchestrate Murine Intestinal Stem Cell Homeostasis

Nicholas R. Smith, Paige Davies, Trevor G. Levin, Alexandra C. Gallagher, Douglas R. Keene, Sidharth K. Sengupta, Nikki Wieghard, Edward El Rassi, Melissa Wong

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Background & Aims Intestinal epithelial homeostasis is maintained by active-cycling and slow-cycling stem cells confined within an instructive crypt-based niche. Exquisite regulating of these stem cell populations along the proliferation-to-differentiation axis maintains a homeostatic balance to prevent hyperproliferation and cancer. Although recent studies focus on how secreted ligands from mesenchymal and epithelial populations regulate intestinal stem cells (ISCs), it remains unclear what role cell adhesion plays in shaping the regulatory niche. Previously we have shown that the cell adhesion molecule and cancer stem cell marker, CD166/ALCAM (activated leukocyte cell adhesion molecule), is highly expressed by both active-cycling Lgr5+ ISCs and adjacent Paneth cells within the crypt base, supporting the hypothesis that CD166 functions to mediate ISC maintenance and signal coordination. Methods Here we tested this hypothesis by analyzing a CD166–/– mouse combined with immunohistochemical, flow cytometry, gene expression, and enteroid culture. Results We found that animals lacking CD166 expression harbored fewer active-cycling Lgr5+ ISCs. Homeostasis was maintained by expansion of the transit-amplifying compartment and not by slow-cycling Bmi1+ ISC stimulation. Loss of active-cycling ISCs was coupled with deregulated Paneth cell homeostasis, manifested as increased numbers of immature Paneth progenitors due to decreased terminal differentiation, linked to defective Wnt signaling. CD166–/– Paneth cells expressed reduced Wnt3 ligand expression and depleted nuclear β-catenin. Conclusions These data support a function for CD166 as an important cell adhesion molecule that shapes the signaling microenvironment by mediating ISC–niche cell interactions. Furthermore, loss of CD166 expression results in decreased ISC and Paneth cell homeostasis and an altered Wnt microenvironment.

Original languageEnglish (US)
Pages (from-to)389-409
Number of pages21
JournalCMGH
Volume3
Issue number3
DOIs
StatePublished - May 1 2017

Fingerprint

Activated-Leukocyte Cell Adhesion Molecule
Cell Adhesion Molecules
Homeostasis
Stem Cells
Paneth Cells
Ligands
Catenins
Neoplastic Stem Cells
Cell Adhesion
Cell Communication
Population
Flow Cytometry

Keywords

  • CD166
  • Homeostasis
  • Intestinal Stem Cell
  • Paneth Cell
  • Stem Cell Niche

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology

Cite this

Cell Adhesion Molecule CD166/ALCAM Functions Within the Crypt to Orchestrate Murine Intestinal Stem Cell Homeostasis. / Smith, Nicholas R.; Davies, Paige; Levin, Trevor G.; Gallagher, Alexandra C.; Keene, Douglas R.; Sengupta, Sidharth K.; Wieghard, Nikki; El Rassi, Edward; Wong, Melissa.

In: CMGH, Vol. 3, No. 3, 01.05.2017, p. 389-409.

Research output: Contribution to journalArticle

Smith, NR, Davies, P, Levin, TG, Gallagher, AC, Keene, DR, Sengupta, SK, Wieghard, N, El Rassi, E & Wong, M 2017, 'Cell Adhesion Molecule CD166/ALCAM Functions Within the Crypt to Orchestrate Murine Intestinal Stem Cell Homeostasis', CMGH, vol. 3, no. 3, pp. 389-409. https://doi.org/10.1016/j.jcmgh.2016.12.010
Smith, Nicholas R. ; Davies, Paige ; Levin, Trevor G. ; Gallagher, Alexandra C. ; Keene, Douglas R. ; Sengupta, Sidharth K. ; Wieghard, Nikki ; El Rassi, Edward ; Wong, Melissa. / Cell Adhesion Molecule CD166/ALCAM Functions Within the Crypt to Orchestrate Murine Intestinal Stem Cell Homeostasis. In: CMGH. 2017 ; Vol. 3, No. 3. pp. 389-409.
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AU - Levin, Trevor G.

AU - Gallagher, Alexandra C.

AU - Keene, Douglas R.

AU - Sengupta, Sidharth K.

AU - Wieghard, Nikki

AU - El Rassi, Edward

AU - Wong, Melissa

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