Figure 5
Figure 5. Proposed morphogenic mechanism mediated by MMP2. Our working hypothesis is that LEC behavior is driven by physical constraints imposed by the matrix barrier. Lymphatic vessel elongation and/or branching are dictated by the composition of ECM components, the quantity and cross-linking of the components and where they are situated around the developing vessels. The structural and molecular determinants promote: (1) a stationary phenotype in dense matrix; (2) a bifurcation in case of local matrix deposition as delineated by * (see also Figure 4I-J); and (3) a mesenchymal-like migratory phenotype in case of controlled matrix degradation.

Proposed morphogenic mechanism mediated by MMP2. Our working hypothesis is that LEC behavior is driven by physical constraints imposed by the matrix barrier. Lymphatic vessel elongation and/or branching are dictated by the composition of ECM components, the quantity and cross-linking of the components and where they are situated around the developing vessels. The structural and molecular determinants promote: (1) a stationary phenotype in dense matrix; (2) a bifurcation in case of local matrix deposition as delineated by * (see also Figure 4I-J); and (3) a mesenchymal-like migratory phenotype in case of controlled matrix degradation.

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