TY - JOUR
T1 - An Integrated Transcriptome Atlas of Embryonic Hair Follicle Progenitors, Their Niche, and the Developing Skin
AU - Sennett, Rachel
AU - Wang, Zichen
AU - Rezza, Amélie
AU - Grisanti, Laura
AU - Roitershtein, Nataly
AU - Sicchio, Cristina
AU - Mok, Ka Wai
AU - Heitman, Nicholas J.
AU - Clavel, Carlos
AU - Ma'ayan, Avi
AU - Rendl, Michael
N1 - Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015/9/14
Y1 - 2015/9/14
N2 - Defining the unique molecular features of progenitors and their niche requires a genome-wide, whole-tissue approach with cellular resolution. Here, we co-isolate embryonic hair follicle (HF) placode and dermal condensate cells, precursors of adult HF stem cells and the dermal papilla/sheath niche, along with lineage-related keratinocytes and fibroblasts, Schwann cells, melanocytes, and a population inclusive of all remaining skin cells. With next-generation RNA sequencing, we define gene expression patterns in the context of the entire embryonic skin, and through transcriptome cross-comparisons, we uncover hundreds of enriched genes in cell-type-specific signatures. Axon guidance signaling and many other pathway genes are enriched in multiple signatures, implicating these factors in driving the large-scale cellular rearrangements necessary for HF formation. Finally, we share all data in an interactive, searchable companion website. Our study provides an overarching view of signaling within the entire embryonic skin and captures a molecular snapshot of HF progenitors and their niche.
AB - Defining the unique molecular features of progenitors and their niche requires a genome-wide, whole-tissue approach with cellular resolution. Here, we co-isolate embryonic hair follicle (HF) placode and dermal condensate cells, precursors of adult HF stem cells and the dermal papilla/sheath niche, along with lineage-related keratinocytes and fibroblasts, Schwann cells, melanocytes, and a population inclusive of all remaining skin cells. With next-generation RNA sequencing, we define gene expression patterns in the context of the entire embryonic skin, and through transcriptome cross-comparisons, we uncover hundreds of enriched genes in cell-type-specific signatures. Axon guidance signaling and many other pathway genes are enriched in multiple signatures, implicating these factors in driving the large-scale cellular rearrangements necessary for HF formation. Finally, we share all data in an interactive, searchable companion website. Our study provides an overarching view of signaling within the entire embryonic skin and captures a molecular snapshot of HF progenitors and their niche.
UR - http://www.scopus.com/inward/record.url?scp=84942321277&partnerID=8YFLogxK
U2 - 10.1016/j.devcel.2015.06.023
DO - 10.1016/j.devcel.2015.06.023
M3 - Article
C2 - 26256211
AN - SCOPUS:84942321277
SN - 1534-5807
VL - 34
SP - 577
EP - 591
JO - Developmental Cell
JF - Developmental Cell
IS - 5
M1 - 3377
ER -