Fibronectin EIIIA splice variant promotes liver sinusoid repair following hepatectomy

Liver sinusoidal endothelial cells (LSECs) are the main endothelial cells in the liver and are important for maintaining liver homeostasis as well as responding to injury. LSECs express cellular fibronectin containing the alternatively spliced extra domain A (EIIIA) and increase expression of this isoform in response to liver injury, although its function is not well understood. Here, I examined the role of EIIIA in sinusoid repair and liver regeneration by carrying out partial hepatectomies in mice lacking EIIIA or their wild type littermates. In vitro, I studied LSEC adhesion on decellularized, EIIIA-containing matrices and investigated the role of cellular fibronectins in LSEC tubulogenesis. I found that liver regeneration was significantly delayed and that sinusoidal repair was impaired in EIIIA-/- mice, especially females, as was the lipid accumulation typical of the post-hepatectomy liver. In vitro, I observed that primary LSECs were more adhesive to cell-deposited matrices containing EIIIA and that cellular fibronectin enhanced LSEC tubulogenesis and vascular cord formation. The integrin α9β1 , which specifically binds EIIIA, promoted adhesion of LSECs to EIIIA and tubulogenesis. My graduate project’s findings identify a role for EIIIA in liver regeneration. The study suggests that sinusoidal repair and the ability to deliver lipids mobilized from peripheral stores as an energy source for regeneration is enhanced by increased LSEC adhesion, which is mediated by EIIIA

Fibronectin Extra Domain A Promotes Liver Sinusoid Repair following Hepatectomy.

Liver sinusoidal endothelial cells (LSECs) are the main endothelial cells in the liver and are important for maintaining liver homeostasis as well as responding to injury. LSECs express cellular fibronectin containing the alternatively spliced extra domain A (EIIIA-cFN) and increase expression of this isoform after liver injury, although its function is not well understood. Here, we examined the role of EIIIA-cFN in liver regeneration following partial hepatectomy. We carried out two-thirds partial hepatectomies in mice lacking EIIIA-cFN and in their wild type littermates, studied liver endothelial cell adhesion on decellularized, EIIIA-cFN-containing matrices and investigated the role of cellular fibronectins in liver endothelial cell tubulogenesis. We found that liver weight recovery following hepatectomy was significantly delayed and that sinusoidal repair was impaired in EIIIA-cFN null mice, especially females, as was the lipid accumulation typical of the post-hepatectomy liver. In vitro, we found that liver endothelial cells were more adhesive to cell-deposited matrices containing the EIIIA domain and that cellular fibronectin enhanced tubulogenesis and vascular cord formation. The integrin α9β1, which specifically binds EIIIA-cFN, promoted tubulogenesis and adhesion of liver endothelial cells to EIIIA-cFN. Our findings identify a role for EIIIA-cFN in liver regeneration and tubulogenesis. We suggest that sinusoidal repair is enhanced by increased LSEC adhesion, which is mediated by EIIIA-cFN

Hepatic stellate cells require a stiff environment for myofibroblastic differentiation

The myofibroblastic differentiation of hepatic stellate cells (HSC) is a critical event in liver fibrosis and is part of the final common pathway to cirrhosis in chronic liver disease from all causes. The molecular mechanisms driving HSC differentiation are not fully understood. Because macroscopic tissue stiffening is a feature of fibrotic disease, we hypothesized that mechanical properties of the underlying matrix are a principal determinant of HSC activation. Primary rat HSC were cultured on inert polyacrylamide supports of variable but precisely defined shear modulus (stiffness) coated with different extracellular matrix proteins or poly-l-lysine. HSC differentiation was determined by cell morphology, immunofluorescence staining, and gene expression. HSC became progressively myofibroblastic as substrate stiffness increased on all coating matrices, including Matrigel. The degree rather than speed of HSC activation correlated with substrate stiffness, with cells cultured on supports of intermediate stiffness adopting stable intermediate phenotypes. Quiescent cells on soft supports were able to undergo myofibroblastic differentiation with exposure to stiff supports. Stiffness-dependent differentiation required adhesion to matrix proteins and the generation of mechanical tension. Transforming growth factor-β treatment enhanced differentiation on stiff supports, but was not required. HSC differentiate to myofibroblasts in vitro primarily as a function of the physical rather than the chemical properties of the substrate. HSC require a mechanically stiff substrate, with adhesion to matrix proteins and the generation of mechanical tension, to differentiate. These findings suggest that alterations in liver stiffness are a key factor driving the progression of fibrosis

Fibronectin Extra Domain A Promotes Liver Sinusoid Repair following Hepatectomy

<div><p>Liver sinusoidal endothelial cells (LSECs) are the main endothelial cells in the liver and are important for maintaining liver homeostasis as well as responding to injury. LSECs express cellular fibronectin containing the alternatively spliced extra domain A (EIIIA-cFN) and increase expression of this isoform after liver injury, although its function is not well understood. Here, we examined the role of EIIIA-cFN in liver regeneration following partial hepatectomy. We carried out two-thirds partial hepatectomies in mice lacking EIIIA-cFN and in their wild type littermates, studied liver endothelial cell adhesion on decellularized, EIIIA-cFN-containing matrices and investigated the role of cellular fibronectins in liver endothelial cell tubulogenesis. We found that liver weight recovery following hepatectomy was significantly delayed and that sinusoidal repair was impaired in EIIIA-cFN null mice, especially females, as was the lipid accumulation typical of the post-hepatectomy liver. <i>In vitro</i>, we found that liver endothelial cells were more adhesive to cell-deposited matrices containing the EIIIA domain and that cellular fibronectin enhanced tubulogenesis and vascular cord formation. The integrin α₉β₁, which specifically binds EIIIA-cFN, promoted tubulogenesis and adhesion of liver endothelial cells to EIIIA-cFN. Our findings identify a role for EIIIA-cFN in liver regeneration and tubulogenesis. We suggest that sinusoidal repair is enhanced by increased LSEC adhesion, which is mediated by EIIIA-cFN.</p></div

EIIIA promotes expression of the vasculature marker VE-cadherin following PHx.

<p>Frozen liver sections taken at day 2 after PHx were stained for VE-cadherin (white). Livers from female and male wild type mice showed increased staining for VE-cadherin <b>(A, C)</b> compared to livers from EIIIA-cFN null mice <b>(B, D)</b>. Scale bar, 50 μm. <b>(E, F)</b> Quantification = minimum to maximum % VE cadherin positive area measurements with line at mean, EIIIA^+/+ (n = 10; 5 female, 5 male); EIIIA^-/- (n = 10; 5 female, 5 male). * p<0.05.</p

Expression of EIIIA-cFN is upregulated early after PHx.

<p><b>(A, B)</b> Wild type mice were euthanized at days 1, 2 and 5 following PHx. mRNA transcript levels for <b>(A)</b> EIIIA-cFN and <b>(B)</b> total fibronectin were measured by qRT-PCR normalized to the expression of <i>tbp</i>. n = 3–4 mice per time point, error bars are mean +/- SEM, *p < 0.05. <b>(C, D)</b> Liver tissue from wild type <b>(C)</b> control mice or <b>(D)</b> mice at day 2 after PHx was stained for EIIIA-cFN (magenta) and with DAPI (blue). Scale bar, 20 μm.</p

Expression of EIIIA-cFN is upregulated early after PHx.

<p><b>(A, B)</b> Wild type mice were euthanized at days 1, 2 and 5 following PHx. mRNA transcript levels for <b>(A)</b> EIIIA-cFN and <b>(B)</b> total fibronectin were measured by qRT-PCR normalized to the expression of <i>tbp</i>. n = 3–4 mice per time point, error bars are mean +/- SEM, *p < 0.05. <b>(C, D)</b> Liver tissue from wild type <b>(C)</b> control mice or <b>(D)</b> mice at day 2 after PHx was stained for EIIIA-cFN (magenta) and with DAPI (blue). Scale bar, 20 μm.</p

Female EIIIA-cFN null mice have decreased accumulation of intracellular lipids at day 2 after PHx.

<p>Frozen liver sections from animals at day 2 following PHx were stained with Oil Red O; lipid droplets (red), hematoxylin (blue). Oil Red O staining was decreased in female EIIIA-cFN null mice <b>(B)</b> in comparison to wild type littermates <b>(A)</b>. Staining for males was comparable between EIIIA-cFN null <b>(D)</b> and wild type littermates <b>(C). (E, F)</b> Quantification of percent Oil Red O covered area, mean +/- SD, * p<0.05. Scale bar, 50 μm. (EIIIA^+/+ = 10; 5 female, 5 male; EIIIA^-/- = 10; 4 female, 6 male).</p