The de novo formation of secretory lumens plays an important role during organogenesis. It involves the establishment of a cellular apical pole(1) and the elongation of luminal cavities(2). The molecular parameters controlling cell polarization have been heavily scrutinized(3-5). In particular, signalling from the extracellular matrix (ECM) proved essential to the proper localization of the apical pole by directed protein transport(6). However, little is known about the regulation of the shape and the directional development of lumen into tubes. We demonstrate that the spatial scaffolding of cells by ECM can control tube shapes and can direct their elongation. We developed a minimal organ approach comprising of hepatocyte doublets cultured in artificial microniches to precisely control the spatial organization of cellular adhesions in three dimensions. This approach revealed a mechanism by which the spatial repartition of integrin-based adhesion can elicit an anisotropic intercellular mechanical stress guiding the osmotically driven elongation of lumens in the direction of minimal tension. This mechanical guidance accounts for the different morphologies of lumen in various microenvironmental conditions.