Loss of MYO5B in Mice Recapitulates Microvillus Inclusion Disease and Reveals an Apical Trafficking Pathway Distinct to Neonatal Duodenum

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• 作者：Victoria G. Weis¹ ; ² ; Byron C. Knowles³ ; ² ; Eunyoung Choi¹ ; ² ; ⁴ ; Anna E. Goldstein¹ ; ² ; Janice A. Williams¹ ; ² ; Elizabeth H. Manning¹ ; ² ; ⁴ ; Joseph T. Roland¹ ; ² ; Lynne A. Lapierre¹ ; ² ; ⁴ ; James R. Goldenring¹ ; ² ; ³ ; ⁴ ; ^{jim.goldenring@vanderbilt.edu" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Enterocyte Trafficking ; Brush Border ; Rab11a ; Rab8a ; Syntaxin 3 ; NHE3 ; MYO5B
• 刊名：CMGH Cellular and Molecular Gastroenterology and Hepatology
• 出版年：2016
• 出版时间：February 2016
• 年：2016
• 卷：2
• 期：2
• 页码：131-157
• 全文大小：12656 K

文摘

Inactivating mutations in myosin Vb (MYO5B) cause severe neonatal diarrhea in microvillus inclusion disease. Loss of active MYO5B causes the formation of pathognomonic inclusions and aberrations in brush-border enzymes.

Methods

We developed 3 mouse models of germline, constitutively intestinal targeted, and inducible intestinal targeted deletion of MYO5B. The mice were evaluated for enterocyte cellular morphology.

Results

Germline MYO5B knockout mice showed early diarrhea and failure to thrive with evident microvillus inclusions and loss of apical transporters in the duodenum. IgG was present within inclusions. Apical transporters were lost and inclusions were present in the duodenum, but were nearly absent in the ileum. VillinCre;MYO5B^F/F mice showed similar pathology and morphologic changes in duodenal enterocytes. In contrast, when MYO5B KO was induced with tamoxifen treatment at 8 weeks of age, VillinCre^ERT2;MYO5B^F/F mice developed severe diarrhea with loss of duodenal brush-border enzymes, but few inclusions were observed in enterocytes. However, if tamoxifen was administered to 2-day-old VillinCre^ERT2;MYO5B^F/F mice, prominent microvillus inclusions were observed.

Conclusions

The microvillus inclusions that develop after MYO5B loss show the presence of an unrecognized apical membrane trafficking pathway in neonatal duodenal enterocytes. However, the diarrheal pathology after MYO5B loss is caused by deficits in transporter presentation at the apical membrane in duodenal enterocytes.