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We read with interest the recent work by Schleier et al 1 demonstrating consequences of impaired α4β7 integrin-dependent gut homing of intestinal macrophages on wound healing, which fits well with own observations we have made in a case of congenital infantile intractable diarrhoea linked to impaired integrin receptors in intestinal epithelia (αVβ6). Specifically, a male dizygotic twin was delivered dystrophic (1715 g) at 36 weeks of gestational age and developed intractable diarrhoea within the following 2 months, contrary to his twin brother. Severe systemic infection or parasitosis was ruled out, but subsequently low-serum IgG and severe neutropenia occurred due to consumption of neutrophils during the prolonged diarrhoea. Eventually, he developed cholestatic hepatopathy and thrombocytopenia and died of uncontrollable GI, dermal haemorrhages and hepatic failure at 7 months of age. Extensive diagnostics included biopsies of liver, muscle, bone marrow, small intestine, the exclusion of known congenital diarrhoea reasons and immunodeficiencies by leucocyte FACS, CD40L expression, WASP staining, et cetera with no results.2 Familial anamnesis revealed similar fatalities of a sister and further cousins from the patient’s known generation within their first year of life due to intractable diarrhoea (figure 1A; 5 fatalities/16 infants).
Using whole exome sequencing on both twins and parents we identified a single-nucleotide polymorphism (SNP) in the integrin beta-6-subunit-encoding gene (ITGB6G1312A|rs61737764) leading to a valine to methionine substitution (ITGB6V438M). The heterodimeric αVβ6 receptor participates in mediating cell-cell and cell-extracellular matrix interactions. Further SNPs fitting to autosomal-recessive inheritance were improbable candidates due to lacking phenotype conformity (DSG4C1568T)3 or relatively high population frequency (TTC3G2771A).4 5 Next, we analysed the relevance of ITGB6V438M by structural simulation, cell-based interaction studies, immunohistochemistry and ITGB6 knockdown in zebrafish. Anti-αVβ6 monoclonal immunohistochemistry revealed diminished intestinal αVβ6,6 7 which correlated with enriched LTBP1, possibly influencing TGF-β1 activation from its latent precursor (figure 1B).8 Evolutionary ITGB6V438 conservation within a hydrophilic motif in mammalian integrin β6 and human integrins β3, β5 and β6 emphasises its relevance (figure 2A). Comparative structure inspection on PDB ID 4UM8|ITGB6(wt)9 suggests that ITGB6V438M could affect the conformational transition between the inactive bent stage and the activated open conformation by establishing additional intramolecular hydrogen bonds (figure 2B1–3),8 10 possibly impairing proper αV/β6 subunit interactions. To study the impact of ITGB6V438M on heterodimerisation we used fluorescent two-hybrid assays in hamster cells. Both subunits colocalised when ITGB6(wt)-GFP2 and ITGAV-RFP were cotransfected (figure 2C, top), but not when ITGB6V438M-GFP2 was cotransfected with ITGAV-RFP (figure 2C, bottom). Finally, ITGB6 morpholino injection led to altered tailfin epithelia recovery after standardised injuries in zebrafish embryos with significant delays in wound recovery when morpholinos were used at 0.3, 0.6 or 0.9 mM after 24 hours and increased mortality after 48 hours above 0.9 mM, supporting a role of ITGB6 in tissue integrity (figure 2D1–5). We propose that improper conformational transition of αVβ6 integrin receptors affects intestinal tissue integrity and barrier function explaining both diarrhoea and haemorrhages.
We thank the children and their parents for their participation in this study. We further thank Paul Weinreb, Biogen, Cambridge, MA, USA, for donating anti-αVβ6 mAbs (clone 6.2A1), Philipp Schreiner, Silvia Vogel, Frauke Schuster and Hubert Zirngibl for their support and scientific input.
We thank the Vereinigung Rheinisch-Westfälischer Kinder- und Jugendärzte und Kinderchirurgen eV (RWKJK) for awarding this study.
AJ and JP are joint last authors.
ACJ and JP contributed equally.
Contributors ACJ, SW and RvdB collected the patient material. ACJ and JP performed the study design and coordinated the experiments. PW performed the exome sequencing and the in silico analysis. PW and VO performed the cell culture studies. DG performed the immunohistochemistry. TZ and SJ performed the zebra fish studies. ACJ and JP wrote the manuscript.
Funding This work was supported by HELIOS Research Center, Berlin, Germany (HRC IDs 009694 and 060721).
Disclaimer The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests None declared.
Provenance and peer review Not commissioned; internally peer reviewed.
Patient consent for publication Not required.
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