TY - JOUR
T1 - Spatial transcriptomics reveals asymmetric cellular responses to injury in the regenerating spiny mouse (Acomys) ear
AU - van Beijnum, Henriëtte
AU - Koopmans, Tim
AU - Tomasso, Antonio
AU - Disela, Vanessa
AU - te Lindert, Severin
AU - Bakkers, Jeroen
AU - Alemany, Anna
AU - Berezikov, Eugene
AU - Bartscherer, Kerstin
N1 - Publisher Copyright:
© 2023 van Beijnum et al.
PY - 2023/8
Y1 - 2023/8
N2 - In contrast to other mammals, the spiny mouse (Acomys) regenerates skin and ear tissue, which includes hair follicles, glands, and cartilage, in a scar-free manner. Ear punch regeneration is asymmetric with only the proximal wound side participating in regeneration. Here, we show that cues originating from the proximal side are required for normal regeneration and use spatially resolved transcriptomics (tomo-seq) to understand the molecular and cellular events underlying this process. Analyzing gene expression across the ear and comparing expression modules between proximal and distal wound sides, we identify asymmetric gene expression patterns and pinpoint regenerative processes in space and time. Moreover, using a comparative approach with nonregenerative rodents (Mus, Meriones), we strengthen a hypothesis in which particularities in the injury-induced immune response may be one of the crucial determinants for why spiny mice regenerate whereas their relatives do not. Our data are available in SpinyMine, an easy-to-use and expandable web-based tool for exploring Acomys regeneration-associated gene expression.
AB - In contrast to other mammals, the spiny mouse (Acomys) regenerates skin and ear tissue, which includes hair follicles, glands, and cartilage, in a scar-free manner. Ear punch regeneration is asymmetric with only the proximal wound side participating in regeneration. Here, we show that cues originating from the proximal side are required for normal regeneration and use spatially resolved transcriptomics (tomo-seq) to understand the molecular and cellular events underlying this process. Analyzing gene expression across the ear and comparing expression modules between proximal and distal wound sides, we identify asymmetric gene expression patterns and pinpoint regenerative processes in space and time. Moreover, using a comparative approach with nonregenerative rodents (Mus, Meriones), we strengthen a hypothesis in which particularities in the injury-induced immune response may be one of the crucial determinants for why spiny mice regenerate whereas their relatives do not. Our data are available in SpinyMine, an easy-to-use and expandable web-based tool for exploring Acomys regeneration-associated gene expression.
UR - http://www.scopus.com/inward/record.url?scp=85172941343&partnerID=8YFLogxK
U2 - 10.1101/gr.277538.122
DO - 10.1101/gr.277538.122
M3 - Article
C2 - 37726147
AN - SCOPUS:85172941343
SN - 1088-9051
VL - 33
SP - 1424
EP - 1437
JO - Genome Research
JF - Genome Research
IS - 8
ER -