“…[281] Such fibers encapsulated differentiated cells or somatic stem cells, were enriched with ECM proteins, and could be assembled into constructs that replicated the intrinsic morphologies and functions of living tissues, such as, muscle fibers, blood vessels, and nerve networks. In Table 3, some examples of cell-laden microfibers generated by the microfluidic laminar flow method are listed, which include microfibers derived from alginate, [366][367][368][369][370][371][372][373][374][375] modified or enriched alginate, [359,[376][377][378][379][380][381] and other biomaterials. [224,281,322,361,382] Some examples of microfluidically generated microfibers are represented in Figure 9 that depicts: Microfibers composed of a single biomaterial whose different diameters affect the alignment of adherent cells (Figure 9A); [359] microfibers whose heterogeneous biomaterial composition increases cell viability (Figure 9B); [361] microfibers with grooved microstructures that facilitate cell alignment (Figure 9C); [378] microfibers encapsulating different cell populations (Figure 9D); [377] microfibers with tailorable internal architectures and hollow cavities, and assemblable into complex 3D geometries (Figure 9E), demonstrating that through multiple-laminar-flow microfluidics, it is possible to prepare multicomponent 3D alginate microfibers in which the morphology of the encapsulated cells can be precisely controlled.…”