Limits...
Suppression of anoikis in human intestinal epithelial cells: differentiation state-selective roles of α2β1, α3β1, α5β1, and α6β4 integrins.

Beauséjour M, Thibodeau S, Demers MJ, Bouchard V, Gauthier R, Beaulieu JF, Vachon PH - BMC Cell Biol. (2013)

Bottom Line: Activation levels of Fak and Src, as well as functional Fak-Src interactions, were also assessed.We report herein that differentiated IECs exhibit a greater sensitivity to anoikis than undifferentiated ones.Additionally, we show that α2β1 and α5β1 suppress anoikis in undifferentiated cells, whereas α3β1 does so in differentiated ones.

View Article: PubMed Central - HTML - PubMed

Affiliation: Département d'anatomie et de biologie cellulaire, Faculté de médecine et des sciences de la santé, Université de Sherbrooke, J1H5N4 Sherbrooke, Québec, Canada. Pierre.H.Vachon@USherbrooke.ca.

ABSTRACT

Background: Regulation of anoikis in human intestinal epithelial cells (IECs) implicates differentiation state-specific mechanisms. Human IECs express distinct repertoires of integrins according to their state of differentiation. Therefore, we investigated whether α2β1, α3β1, α5β1, and α6β4 integrins perform differentiation state-specific roles in the suppression of IEC anoikis.

Results: Human (HIEC, Caco-2/15) IECs were exposed to specific antibodies that block the binding activity of integrin subunits (α2, α3, α5, α6, β1 or β4) to verify whether or not their inhibition induced anoikis. The knockdown of α6 was also performed by shRNA. Additionally, apoptosis/anoikis was induced by pharmacological inhibition of Fak (PF573228) or Src (PP2). Anoikis/apoptosis was assayed by DNA laddering, ISEL, and/or caspase activity (CASP-8, -9, or -3). Activation levels of Fak and Src, as well as functional Fak-Src interactions, were also assessed. We report herein that differentiated IECs exhibit a greater sensitivity to anoikis than undifferentiated ones. This involves an earlier onset of anoikis when kept in suspension, as well as significantly greater contributions from β1 and β4 integrins in the suppression of anoikis in differentiated cells, and functional distinctions between β1 and β4 integrins in engaging both Fak and Src, or Src only, respectively. Likewise, Fak performs significantly greater contributions in the suppression of anoikis in differentiated cells. Additionally, we show that α2β1 and α5β1 suppress anoikis in undifferentiated cells, whereas α3β1 does so in differentiated ones. Furthermore, we provide evidence that α6β4 contributes to the suppression of anoikis in a primarily α6 subunit-dependent manner in undifferentiated cells, whereas this same integrin in differentiated cells performs significantly greater contributions in anoikis suppression than its undifferentiated state-counterpart, in addition to doing so through a dependence on both of its subunits.

Conclusions: Our findings indicate that the suppression of human IEC anoikis implicates differentiation state-selective repertoires of integrins, which in turn results into distinctions in anoikis regulation, and sensitivity, between undifferentiated and differentiated IECs. These data further the functional understanding of the concept that the suppression of anoikis is subjected to cell differentiation state-selective mechanisms.

Show MeSH

Related in: MedlinePlus

Differentiation state-distinct contributions of α2, α3, α5 and α6 integrin subunits, in the suppression of human IEC anoikis. A. Representative (n ≥ 3) double labeling-merged immunofluorescence micrographs of adhering HIEC cell cultures maintained 24 h serum-free (control) with mouse IgG’s, P1E6 (α2 binding activity-blocking mAb), P1D6 (α5 binding activity-blocking mAb), or GoH3 (α6 binding activity-blocking mAb). ISEL (green) was thereafter performed, with DAPI (blue) counter-staining of nuclei. B. Same as in (A), except that adhering 30PC Caco-2/15 cells were maintained 24 h serum-free (control) with mouse IgG’s, P1B5 (α3 binding activity-blocking mAb), P1D6 (α5 binding activity-blocking mAb), or GoH3 (α6 binding activity-blocking mAb). C. Adhering HIEC (Undifferentiated; filled columns) and 30PC Caco-2/15 (Differentiated; open columns) cell cultures were maintained 24 h serum-free (control) with mouse IgG’s, P1E6, P1B5, P1D6, or GoH3. ISEL assays were performed and compared to controls. Statistically significant (0.0001 ≤ P ≤ 0.001; n ≥ 3) differences between treated and control cultures are indicated by (*). Statistically significant (0.0005 ≤ P ≤ 0.005; n ≥ 3) differences between differentiated and undifferentiated IECs are indicated by (#). A-B. Original magnifications: 20X. A, C. Results obtained with -2PC Caco-2/15 cells were highly similar to those shown here for HIEC cells.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
getmorefigures.php?uid=PMC4219346&req=5

Figure 6: Differentiation state-distinct contributions of α2, α3, α5 and α6 integrin subunits, in the suppression of human IEC anoikis. A. Representative (n ≥ 3) double labeling-merged immunofluorescence micrographs of adhering HIEC cell cultures maintained 24 h serum-free (control) with mouse IgG’s, P1E6 (α2 binding activity-blocking mAb), P1D6 (α5 binding activity-blocking mAb), or GoH3 (α6 binding activity-blocking mAb). ISEL (green) was thereafter performed, with DAPI (blue) counter-staining of nuclei. B. Same as in (A), except that adhering 30PC Caco-2/15 cells were maintained 24 h serum-free (control) with mouse IgG’s, P1B5 (α3 binding activity-blocking mAb), P1D6 (α5 binding activity-blocking mAb), or GoH3 (α6 binding activity-blocking mAb). C. Adhering HIEC (Undifferentiated; filled columns) and 30PC Caco-2/15 (Differentiated; open columns) cell cultures were maintained 24 h serum-free (control) with mouse IgG’s, P1E6, P1B5, P1D6, or GoH3. ISEL assays were performed and compared to controls. Statistically significant (0.0001 ≤ P ≤ 0.001; n ≥ 3) differences between treated and control cultures are indicated by (*). Statistically significant (0.0005 ≤ P ≤ 0.005; n ≥ 3) differences between differentiated and undifferentiated IECs are indicated by (#). A-B. Original magnifications: 20X. A, C. Results obtained with -2PC Caco-2/15 cells were highly similar to those shown here for HIEC cells.

Mentions: As assessed by ISEL, the inhibition of the α2 integrin subunit induced significant cell death in undifferentiated cells, but not in differentiated ones (Figure 6A, C). Likewise, the inhibition of α5 produced significant anoikis in undifferentiated IECs only (Figure 6A-C). By contrast, the inhibition of α3 induced significant cell death in differentiated IECs, but not in undifferentiated ones (Figure 6B-C). Finally, the inhibition of α6 produced abundant anoikis regardless of the state of differentiation, although its impact to this effect was significantly greater in differentiated cells (Figure 6A-C).


Suppression of anoikis in human intestinal epithelial cells: differentiation state-selective roles of α2β1, α3β1, α5β1, and α6β4 integrins.

Beauséjour M, Thibodeau S, Demers MJ, Bouchard V, Gauthier R, Beaulieu JF, Vachon PH - BMC Cell Biol. (2013)

Differentiation state-distinct contributions of α2, α3, α5 and α6 integrin subunits, in the suppression of human IEC anoikis. A. Representative (n ≥ 3) double labeling-merged immunofluorescence micrographs of adhering HIEC cell cultures maintained 24 h serum-free (control) with mouse IgG’s, P1E6 (α2 binding activity-blocking mAb), P1D6 (α5 binding activity-blocking mAb), or GoH3 (α6 binding activity-blocking mAb). ISEL (green) was thereafter performed, with DAPI (blue) counter-staining of nuclei. B. Same as in (A), except that adhering 30PC Caco-2/15 cells were maintained 24 h serum-free (control) with mouse IgG’s, P1B5 (α3 binding activity-blocking mAb), P1D6 (α5 binding activity-blocking mAb), or GoH3 (α6 binding activity-blocking mAb). C. Adhering HIEC (Undifferentiated; filled columns) and 30PC Caco-2/15 (Differentiated; open columns) cell cultures were maintained 24 h serum-free (control) with mouse IgG’s, P1E6, P1B5, P1D6, or GoH3. ISEL assays were performed and compared to controls. Statistically significant (0.0001 ≤ P ≤ 0.001; n ≥ 3) differences between treated and control cultures are indicated by (*). Statistically significant (0.0005 ≤ P ≤ 0.005; n ≥ 3) differences between differentiated and undifferentiated IECs are indicated by (#). A-B. Original magnifications: 20X. A, C. Results obtained with -2PC Caco-2/15 cells were highly similar to those shown here for HIEC cells.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC4219346&req=5

Figure 6: Differentiation state-distinct contributions of α2, α3, α5 and α6 integrin subunits, in the suppression of human IEC anoikis. A. Representative (n ≥ 3) double labeling-merged immunofluorescence micrographs of adhering HIEC cell cultures maintained 24 h serum-free (control) with mouse IgG’s, P1E6 (α2 binding activity-blocking mAb), P1D6 (α5 binding activity-blocking mAb), or GoH3 (α6 binding activity-blocking mAb). ISEL (green) was thereafter performed, with DAPI (blue) counter-staining of nuclei. B. Same as in (A), except that adhering 30PC Caco-2/15 cells were maintained 24 h serum-free (control) with mouse IgG’s, P1B5 (α3 binding activity-blocking mAb), P1D6 (α5 binding activity-blocking mAb), or GoH3 (α6 binding activity-blocking mAb). C. Adhering HIEC (Undifferentiated; filled columns) and 30PC Caco-2/15 (Differentiated; open columns) cell cultures were maintained 24 h serum-free (control) with mouse IgG’s, P1E6, P1B5, P1D6, or GoH3. ISEL assays were performed and compared to controls. Statistically significant (0.0001 ≤ P ≤ 0.001; n ≥ 3) differences between treated and control cultures are indicated by (*). Statistically significant (0.0005 ≤ P ≤ 0.005; n ≥ 3) differences between differentiated and undifferentiated IECs are indicated by (#). A-B. Original magnifications: 20X. A, C. Results obtained with -2PC Caco-2/15 cells were highly similar to those shown here for HIEC cells.
Mentions: As assessed by ISEL, the inhibition of the α2 integrin subunit induced significant cell death in undifferentiated cells, but not in differentiated ones (Figure 6A, C). Likewise, the inhibition of α5 produced significant anoikis in undifferentiated IECs only (Figure 6A-C). By contrast, the inhibition of α3 induced significant cell death in differentiated IECs, but not in undifferentiated ones (Figure 6B-C). Finally, the inhibition of α6 produced abundant anoikis regardless of the state of differentiation, although its impact to this effect was significantly greater in differentiated cells (Figure 6A-C).

Bottom Line: Activation levels of Fak and Src, as well as functional Fak-Src interactions, were also assessed.We report herein that differentiated IECs exhibit a greater sensitivity to anoikis than undifferentiated ones.Additionally, we show that α2β1 and α5β1 suppress anoikis in undifferentiated cells, whereas α3β1 does so in differentiated ones.

View Article: PubMed Central - HTML - PubMed

Affiliation: Département d'anatomie et de biologie cellulaire, Faculté de médecine et des sciences de la santé, Université de Sherbrooke, J1H5N4 Sherbrooke, Québec, Canada. Pierre.H.Vachon@USherbrooke.ca.

ABSTRACT

Background: Regulation of anoikis in human intestinal epithelial cells (IECs) implicates differentiation state-specific mechanisms. Human IECs express distinct repertoires of integrins according to their state of differentiation. Therefore, we investigated whether α2β1, α3β1, α5β1, and α6β4 integrins perform differentiation state-specific roles in the suppression of IEC anoikis.

Results: Human (HIEC, Caco-2/15) IECs were exposed to specific antibodies that block the binding activity of integrin subunits (α2, α3, α5, α6, β1 or β4) to verify whether or not their inhibition induced anoikis. The knockdown of α6 was also performed by shRNA. Additionally, apoptosis/anoikis was induced by pharmacological inhibition of Fak (PF573228) or Src (PP2). Anoikis/apoptosis was assayed by DNA laddering, ISEL, and/or caspase activity (CASP-8, -9, or -3). Activation levels of Fak and Src, as well as functional Fak-Src interactions, were also assessed. We report herein that differentiated IECs exhibit a greater sensitivity to anoikis than undifferentiated ones. This involves an earlier onset of anoikis when kept in suspension, as well as significantly greater contributions from β1 and β4 integrins in the suppression of anoikis in differentiated cells, and functional distinctions between β1 and β4 integrins in engaging both Fak and Src, or Src only, respectively. Likewise, Fak performs significantly greater contributions in the suppression of anoikis in differentiated cells. Additionally, we show that α2β1 and α5β1 suppress anoikis in undifferentiated cells, whereas α3β1 does so in differentiated ones. Furthermore, we provide evidence that α6β4 contributes to the suppression of anoikis in a primarily α6 subunit-dependent manner in undifferentiated cells, whereas this same integrin in differentiated cells performs significantly greater contributions in anoikis suppression than its undifferentiated state-counterpart, in addition to doing so through a dependence on both of its subunits.

Conclusions: Our findings indicate that the suppression of human IEC anoikis implicates differentiation state-selective repertoires of integrins, which in turn results into distinctions in anoikis regulation, and sensitivity, between undifferentiated and differentiated IECs. These data further the functional understanding of the concept that the suppression of anoikis is subjected to cell differentiation state-selective mechanisms.

Show MeSH
Related in: MedlinePlus