Page 32 - IJB-7-3
P. 32

3D Bioprinted Organoids
                         A





















                         B










                         C












           Figure 5. (A) HE staining of the small intestinal crypt was performed on days 3 and 5 (dpi) after irradiation. The green arrow between the
           two dashed lines indicates the length of the crypt. (B) Typical morphology of intestinal organoids cultured under the indicated conditions.
           (C) Schematic diagram of small intestine organoid culture in plant-based nanocellulose hydrogel. (from ref.  licensed under Creative
                                                                                           [57]
           Commons Attribution 4.0 license) and  (from ref.  licensed under Creative Commons Attribution 4.0 license).
                                              [58]
           the tumor microenvironments  by precisely controlling   subtypes)that can help in the understanding of the genesis

           the  combination  of  tumor-associated  cells  and  ECM   and  pathogenesis  of colorectal  tumors,  and  provide
           components and organizing them into well-defined spatial   insights  for  promoting  patient-centered  treatment .
                                                                                                            [66]
           distributions. As the field of precision medicine and the   However, the currently established tumor models do not
           development of organoid culture techniques continue to   accurately  simulate  the  natural  ECM  components  and
           advance, tumor organoid models are being studied at an   interactions between tissue, cell, and matrix molecules.
           increasingly rapid pace. [64]                       The  introduction  of  bioprinting  has  slightly  enhanced
               Recently,  various  tumor  organoid  models  have   the structure of blood vessels and lymphatic vessels in
           been successfully established. Clevers et al. described a   tumor models, as well as the lesion characteristics. Zhao
           strategy for producing 3D prostate organoid cultures from   et al. used bioprinting to construct the first in vitro 3D
           healthy mice and human prostate cells (single lumen and
           basal cells sorted in bulk or FACS), metastatic prostate   tumor  model  of  HeLa  cells  (a  type  of  cervical  cancer
                                                                  [67]
           cancer lesions, and circulating tumor cells . This strategy   cell) .  The  tumor  model  better  reflected  the  growth
                                             [65]
           allows for the growth of intraluminal and basal prostate   and development of the tumor in vivo and approximated
           epithelial cell lines, as well as that of advanced prostate   the lesion characteristics  of the cancer  cells  in vivo
           cancer. Fujii et al. established a model library containing   (Figure 6A, B, C and D). To accurately simulate the
           55 colorectal tumor organoids (including different tumor   complex  microenvironment  of  a  tumor,  Zhang  et al.

           28                          International Journal of Bioprinting (2021)–Volume 7, Issue 3
   27   28   29   30   31   32   33   34   35   36   37