This work is a continuation of our long-standing efforts to understand the formation of the vertebrate limb. The hope is that the knowledge we glean will ultimately provide insights into the developmental defects leading to congenital malformations and to novel regenerative therapies to restore injured appendages. While replacement of developed limb tissues could, in principle, be achieved by harnessing and enhancing the endogenous regenerative potential of the limb through a process akin to amphibian limb regeneration, an alternative approach is to attempt to recapitulate embryonic limb development in an adult setting. Towards that end, in preliminary studies, we have taken a reprogramming approach. Screening for a cocktail of transcription factors capable of respecifying mesenchymal cells to a limb progenitor identity, we have evidence that Lhx2, Nmyc, Sall4 and PDRM16 together can convert non-limb fibroblasts into cells with the properties of early limb bud cells, including driving expression of a gene profile mimicking that is seen in the early limb bud, and can imbue cells with the potential to differentiate into the range of cell types found in the developing limb.
In Aim 1, we will characterize these cells in greater detail in vitro to determine how closely they approximate endogenous limb bud progenitors.
In Aim 2, we will interrogate these cells functionally, testing their capacity to form appropriate tissues and structures in vivo. Finally, in Aim 3, we will focus on two of the factors required for putatively reprogramming limb bud progenitor cells, Sall4 and Lhx2, investigating whether they act through the same sets of gene targets during reprogramming as they do during limb bud development. Together, these studies will bring us closer to understanding how to manipulate limb-like cells for regenerative purposes and will also potentially provide new insights into how early limb bud is regulated.
This project is of relevance to public health from the standpoint of regenerative medicine. We have developed techniques for turning adult cells into the type of cells that form limbs in an embryo. The work described herein will study the way they work?important information if they ever are to be used to regrow limbs following injury or amputation.
Kamberov, Yana G; Guhan, Samantha M; DeMarchis, Alessandra et al. (2018) Comparative evidence for the independent evolution of hair and sweat gland traits in primates. J Hum Evol 125:99-105 |
Bryant, Donald M; Johnson, Kimberly; DiTommaso, Tia et al. (2017) A Tissue-Mapped Axolotl De Novo Transcriptome Enables Identification of Limb Regeneration Factors. Cell Rep 18:762-776 |
Tschopp, Patrick; Tabin, Clifford J (2017) Deep homology in the age of next-generation sequencing. Philos Trans R Soc Lond B Biol Sci 372: |
Hiscock, Tom W; Tschopp, Patrick; Tabin, Clifford J (2017) On the Formation of Digits and Joints during Limb Development. Dev Cell 41:459-465 |
Wark, Abigail R; Terman, Elizabeth J; Tabin, Clifford J (2017) miR-128-1 is not required for hair pigmentation in mice. Exp Dermatol 26:940-942 |
Chen, J W; Galloway, J L (2017) Using the zebrafish to understand tendon development and repair. Methods Cell Biol 138:299-320 |
Young, John J; Tabin, Clifford J (2017) Saunders's framework for understanding limb development as a platform for investigating limb evolution. Dev Biol 429:401-408 |
Lau, Mei Sheng; Schwartz, Matthew G; Kundu, Sharmistha et al. (2017) Mutation of a nucleosome compaction region disrupts Polycomb-mediated axial patterning. Science 355:1081-1084 |
Rodrigues, Alan R; Yakushiji-Kaminatsui, Nayuta; Atsuta, Yuji et al. (2017) Integration of Shh and Fgf signaling in controlling Hox gene expression in cultured limb cells. Proc Natl Acad Sci U S A 114:3139-3144 |
Uygur, Aysu; Young, John; Huycke, Tyler R et al. (2016) Scaling Pattern to Variations in Size during Development of the Vertebrate Neural Tube. Dev Cell 37:127-35 |
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