TY - JOUR
T1 - Nerve independent limb induction in axolotls
AU - Makanae, Aki
AU - Hirata, Ayako
AU - Honjo, Yasuko
AU - Mitogawa, Kazumasa
AU - Satoh, Akira
N1 - Funding Information:
We are grateful to PRESTO members, especially Dr. S. Nishikawa for helpful and fruitful comments and discussions. And we also thank Dr. T. Yamada for his kind supports, and Dr. D.M. Gardiner for constructive discussions on this paper. The authors would like to thank Enago ( www.enago.jp ) for the english language review. This work was supported by JST PRESTO (understanding life by iPS cells technology) to A.S. and KAKENHI ( #23124508 to A.S.). The funders had no role in the study of design, data collection and analysis, decision to publish, or preparation of the manuscript. Appendix A
PY - 2013/9/1
Y1 - 2013/9/1
N2 - Urodele amphibians can regenerate their limbs. During limb regeneration, dermal fibroblasts are transformed into undifferentiated cells called blastema cells. These dermis-blastema cells show multipotency. Such so-called endogenous reprogramming of cell differentiation is one of the main targets of amphibian limb regeneration studies. It is well recognized that nerve presence controls the initiation of limb regeneration. Accordingly, nerve factors have been sought in amphibian limb regeneration. To investigate it, a relatively new study system called the accessory limb model (ALM) was developed. Using ALM, two signaling cascades (Fgf and Gdf5 signaling) came under focus. In the present study, Growth and differentiation factor-5 (Gdf5) application to wounded skin initiated limb regeneration responses and resulted in induction of a blastema-like structure in the absence of a nerve. However, the Gdf5-induced structure showed defects as a regeneration blastema, such as absence of detectable Prrx1 expression by in situ hybridization. The defects could be remedied by additional Fibroblasts growth factor (Fgf) inputs. These two inputs (Gdf5 and Fgfs) were sufficient to substitute for the nerve functions in the induction of limb regeneration. Indeed, Fgf2, Fgf8, and Gdf5 applications with the contralateral skin graft resulted in limb formation without nerve supply. Furthermore, acquisition of cartilage differentiation potential of dermal fibroblasts was tested in an in vivo and in vitro combination assay. Dermal fibroblasts cultured with Gdf5 were difficult to participate in cartilage formation when the cultured cells were grafted into cartilage forming region. In contrast, dermal fibroblasts cultured with Fgf2 and Fgf8 became easier to participate into cartilage formation in the same procedure. These results contribute to our understanding of molecular mechanisms of the early phase of amphibian limb regeneration.
AB - Urodele amphibians can regenerate their limbs. During limb regeneration, dermal fibroblasts are transformed into undifferentiated cells called blastema cells. These dermis-blastema cells show multipotency. Such so-called endogenous reprogramming of cell differentiation is one of the main targets of amphibian limb regeneration studies. It is well recognized that nerve presence controls the initiation of limb regeneration. Accordingly, nerve factors have been sought in amphibian limb regeneration. To investigate it, a relatively new study system called the accessory limb model (ALM) was developed. Using ALM, two signaling cascades (Fgf and Gdf5 signaling) came under focus. In the present study, Growth and differentiation factor-5 (Gdf5) application to wounded skin initiated limb regeneration responses and resulted in induction of a blastema-like structure in the absence of a nerve. However, the Gdf5-induced structure showed defects as a regeneration blastema, such as absence of detectable Prrx1 expression by in situ hybridization. The defects could be remedied by additional Fibroblasts growth factor (Fgf) inputs. These two inputs (Gdf5 and Fgfs) were sufficient to substitute for the nerve functions in the induction of limb regeneration. Indeed, Fgf2, Fgf8, and Gdf5 applications with the contralateral skin graft resulted in limb formation without nerve supply. Furthermore, acquisition of cartilage differentiation potential of dermal fibroblasts was tested in an in vivo and in vitro combination assay. Dermal fibroblasts cultured with Gdf5 were difficult to participate in cartilage formation when the cultured cells were grafted into cartilage forming region. In contrast, dermal fibroblasts cultured with Fgf2 and Fgf8 became easier to participate into cartilage formation in the same procedure. These results contribute to our understanding of molecular mechanisms of the early phase of amphibian limb regeneration.
KW - Axolotl
KW - Blastema
KW - Dedifferentiation
KW - Gdf5
KW - Limb regeneration
UR - http://www.scopus.com/inward/record.url?scp=84881553372&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84881553372&partnerID=8YFLogxK
U2 - 10.1016/j.ydbio.2013.05.010
DO - 10.1016/j.ydbio.2013.05.010
M3 - Article
C2 - 23769980
AN - SCOPUS:84881553372
SN - 0012-1606
VL - 381
SP - 213
EP - 226
JO - Developmental Biology
JF - Developmental Biology
IS - 1
ER -