Smooth muscle deletion of Jag1, but not endothelial deletion, leads to jaundice, cholestasis and bile duct paucity. (A) Mating schema for generating J1^SMKO and J1^ECKO mice. (B) J1^SMKO exhibited jaundice and growth retardation from birth. (C) J1^ECKO mice were viable and normal in size and appearance. (D) Kaplan-meier survival analysis of newborn J1^SMKO mice. (E) Weight (mean, in grams) of J1^SMKO, J1^ECKO and J1^WT+Het mice. Bars indicate s.e.m. (F) (Top) Livers of J1^SMKO mice showed hemorrhage (chevrons) and bile deposits (open arrows). (Middle) Hematoxylin and Eosin staining of P7 livers revealed bile ducts in J1^WT and J1^ECKO mice (arrows), and a lack of patent bile ducts (arrowhead), as well as necrosis (broken white line, open arrow), in J1^SMKO mice. (Bottom) Cytokeratin immunostaining of P25 livers indicated bilayered lumenized bile ducts in J1^WT and J1^ECKO (arrows) and non-lumenized ducts in J1^SMKO (open arrows) mice. gb, gall bladder; pv, portal vein. Scale bars: top row, 20 mm; middle and bottom rows, 100 μm.

Loss of Jag1 in portal vein mesenchyme results in defective bile duct morphogenesis. (A-F) During IHBD development, Jag1 was found in the endothelium (arrows) of both mice, but only in the mesenchyme (asterisks) of J1^WT mice. BECs (arrowheads) labeled with wide-spectrum cytokeratin (ws-CK) form a ductal plate alongside Jag1-positive PVM, while the J1^SMKO liver had not yet formed this structure (E). At P3, the J1^WT liver displayed a well-formed bile duct and Jag1 expression (C, arrows) remained in the endothelium, PVM and BECs. J1^SMKO mice lack patent duct formation and showed a single layer of ws-CK positive cells that resembled the primitive ductal plate (pdp) (F, arrowheads). (G) Immunoprecipitation of Jag1 in whole liver lysates from J1^WT and J1^SMKO mice at E14.5, E16.5 and E18.5. Ns, non-specific band. (H) Western blot of isolated endothelium, BECs and PVM from P3 J1^WT and J1^SMKO livers. (I-L′) Jag1 expression (in red) alone in the endothelium and PVM, and co-localized with ws-CK (green) in BECs (I′,J′, arrowheads) of E18.5 and P3 J1^WT livers. (J′,J′) Jag1-positive PVM (asterisks) at P3 (J′ is a higher magnification of J′). (K,K′) J1^SMKO livers maintain Jag1 expression in the endothelium, but no staining was seen in the PVM or the BECs. (L′,L′) At P3, J1^SMKO livers showed Jag1 colocalized with ws-CK in the disorganized BECs (arrowheads), but absent from PVM (L′ is a higher magnification of L′, bracket). bd, bile duct; bec, biliary epithelial cell; dp, ductal plate; en, endothelium; ha, hepatic artery; pdp, primitive ductal plate; pv, portal vein; pvm, portal vein mesenchyme. Scale bars: 50 μm.

Specificity of Cre expression in developing livers. (A-D) SM22-Cre;R26R double transgenic mice were used to trace Cre activity (β-gal staining, blue) during bile duct morphogenesis (cytokeratin, black). At E15.5, BECs (B,B′, arrowheads) aggregate near β-gal-positive mesenchymal cells that form the primitive ductal plate. By E18.5, a few lumenized bile ducts (C,C′, arrows) form within the mesenchyme (red bracket) and continue to develop at P3 (D,D′, arrows). (E) Western blot for Cre on liver lysates from SM22-Cre;R26R and control mice. Non-specific bands (arrowhead) indicate loading. (F) Sequential sections of SM22Cre;Rosa26R E18.5 (F,F′) livers with and without ws-CK staining. Arrowheads indicate BECs. (G-I) Mesenchymal layer thickness was decreased in J1^SMKO livers compared with heterozygous littermates (brackets), and BEC organization was similar to the primitive ductal plate (H, arrowhead). In J1^ECKO livers, the endothelium (I, open arrows), but not the mesenchyme, was β-gal positive. (J) SM22-Cre;R26R adults show persistence of β-gal staining in both endothelial and smooth muscle cells (open arrows), as well as the PVM (red bracket) surrounding mature bile ducts (arrows). ha, hepatic artery; pv, portal vein; Std, molecular weight standard. Scale bars: 100 μm in A-D; 50 μm in A′-D′,F-J.

Expression of Sox9 in J1^SMKO livers is affected by the loss of Jag1. (A-J) Immunostaining revealed delayed onset and reduced numbers of Sox9-positive cells (arrows) in J1^SMKO mice in embryonic and neonatal livers compared with J1^WT mice. (K-R) Hes1 expression (arrows) at E16.5 (N) was present in both J1^WT and J1^SMKO CK19-positive populations, but was still in the single layer in the disorganized BECs of E18.5 J1^SMKO livers (R). bd, bile duct; pv, portal vein.

Loss of Jag1 halts biliary duct tubulogenesis. (A-B′) Cytokeratin 8 (CK8) in P10 J1^WT and J1^SMKO livers (higher magnifications in A′,B′). CK8-positive BECs formed ducts in J1^WT livers (arrows), while J1^SMKO BECs (arrowheads) did not. (C) FACS analysis of P0 livers from J1^WT, J1^SMHet and J1^SMKO mice show a decrease number of BECs in J1^SMKO mice at P10-11. Bars represent mean±s.e.m. ^*P<0.05 (n=3-7 animals per time point). (D) Western blot of E16.5 and P0 sorted BECs from J1^WT and J1^SMKO livers. E-cadherin (E-cad), CK8 and cytokeratin 19 (CK19) were increased in both mice at P0 in relation to E16.5. α-Enolase was used for loading control. (E) Fluorescent immunostaining of CK8 (red) and TOPRO3 (blue) in J1^WT livers at E18.5 and P10. CK8 expression was initially present along the portal side (arrowheads), but expanded when both epithelial layers were present. Keratin filaments in BECs were bundled and visible at E18.5 (open arrows). By P10, BECs were organized into ducts and CK8 expression circumscribed the cells (arrows). (F,G) Ws-CK, (green) colocalized with CK8 and CK19 in J1^WT P10 livers (arrows, fourth panels). By contrast, CK8 expression was widespread and did not fully overlap with ws-CK (F, arrowheads) in J1^SMKO livers. CK19 expression in J1^SMKO livers was present (G) on the portal side of the BEC layer and not on the parenchymal layer where ws-CK was expressed (arrowheads). CK8 and CK19 keratin filaments were less compacted and organized in J1^SMKO BECs (open arrows). pv, portal vein; nt, necrotic tissue. Scale bars: 100 μm in A,B; 50 μm in A′,B′; 50 μm in E (first and third panels); 10 μm in E (second and fourth panels); 50 μm in F,G; 10 μm in F,G (fourth panels).

Jag1 in the PVM is required for BEC spheroid formation. (A) Western blot of Jag1 in PVM cultures from mutant and control mice. (B) Two-dimensional co-cultures containing BECs and PVM do not form spheroids, but 3D co-cultures with PVM, not with dermal fibroblasts (DF) induce clustering of BECs (arrowhead). (C) Wild-type BECs cultured with J1^WT PVM form spheroids (arrows), but failed to compact when co-cultured with J1^SMKO PVM. (D) Quantification of spheroids from multiple cultures (n=5 independent cultures). ^*P≤0.001; error bars represent ±s.e.m. (E-G′) Immunostaining of the 3D cultures showed expression of BEC differentiation markers (ws-CK or CK19, in green). Wild-type BECS cultured with J1^SMKO PVM did not form large spheroids, but did show smaller cell aggregates that expressed ws-CK (open arrow), similar to the clumps of cells around the portal vein seen in vivo (arrows). Scale bars: 100 μm in B,C,F; 50 μm in E-G,G′; 10 μm in E′,F′.

Temporal requirement of Jag1 signaling for morphogenesis of bile ducts. (A) Notch signaling blockade in wild-type co-cultures of PVM and BECs (at E16.5 and P2) with DAPT prevents spheroid formation (arrows) at E16.5 but not at P2. (B) Western blot demonstrates Notch2 activation within BECs after binding to Jag1 peptide (Fc, control). Black arrow indicates intact Notch2; black arrowhead indicates cleaved Notch2. When cultured with J1^SMKO PVM, E16.5 BECs previously activated with soluble Jag1 peptide regained the ability to form spheroids (arrows), whereas BECs treated with Fc control peptide did not. Scale bars: 100 μm in A,B.

Spatial and temporal requirement of Jag1 during IHBD development. BEC specification and initial ductal plate formation occurs in a mesenchymal Jag1-independent manner (steps 1 and 2). Jag1 expression in the PVM controls the complete formation of the second layer of the ductal plate, allowing the BECs to eventually remodel into a lumenized duct. Expansion of PVM also appears to be dependent on Jag1 signaling (steps 3 and 4). Loss of Jag1 expression in the PVM causes duct development to stall midway during ductal plate morphogenesis (step 3), leading to a paucity of bile ducts.