TY - JOUR
T1 - Genetic mosaic analysis indicates that the bulb region of coat hair follicles contains a resident population of several active multipotent epithelial lineage progenitors
AU - Kopan, Raphael
AU - Lee, Jonghyeob
AU - Lin, Meei Hua
AU - Syder, Andrew J.
AU - Kesterson, John
AU - Crutchfield, Neil
AU - Li, Caroline R.
AU - Wu, Wei
AU - Books, Jason
AU - Gordon, Jeffrey I.
N1 - Funding Information:
We are grateful to David Beebe, Rhiner Strorb, Arthur Eisen, Melissa Wong, Emily Garabedian, Jamie Waggoner, Darlene Stewart, and Teresa Tolley for their advice and assistance during the course of these studies. This work was supported by grants from the National Institutes of Health (AR45254 and DK30292). M.H.L. is the recipient of a postdoctoral fellowship from the Dermatology Foundation and Pharmacia–Upjohn.
PY - 2002/2/1
Y1 - 2002/2/1
N2 - The hair follicle represents an excellent model system for exploring the properties of lineage-forming units in a dynamic epithelium containing multiple cell types. During its growth (anagen) phase, the proximal-distal axis of the mouse coat hair (pelage) follicle provides a historical record of all epithelial lineages generated from its resident stem cell population. An unresolved question in the field is whether the bulb region of anagen pelage follicles contains multipotential progenitors and whether their individual contribution to cellular census fluctuates over time. To address this issue, chimeric follicles were harvested in midanagen from three types of genetic mosaic mouse models. Analysis of the distribution of genotypic markers, including digital three-dimensional reconstruction of serially sectioned chimeric follicles, revealed that on average the bulb contains four or fewer active progenitors, each capable of giving rise to all six follicular epithelial fates. Moreover, analysis of mosaic pelage, as well as cultured whisker follicles provided evidence that bulb-associated progenitors can give rise to expanding descendant clones during midanagen, leading to the conclusion that the bulb contains dormant or symmetrically dividing stem cells. This latter feature resembles the behavior of hematopoietic stem cells after bone marrow transplantation, and raises the question of whether this property may be shared by stem cells in other self-renewing epithelia.
AB - The hair follicle represents an excellent model system for exploring the properties of lineage-forming units in a dynamic epithelium containing multiple cell types. During its growth (anagen) phase, the proximal-distal axis of the mouse coat hair (pelage) follicle provides a historical record of all epithelial lineages generated from its resident stem cell population. An unresolved question in the field is whether the bulb region of anagen pelage follicles contains multipotential progenitors and whether their individual contribution to cellular census fluctuates over time. To address this issue, chimeric follicles were harvested in midanagen from three types of genetic mosaic mouse models. Analysis of the distribution of genotypic markers, including digital three-dimensional reconstruction of serially sectioned chimeric follicles, revealed that on average the bulb contains four or fewer active progenitors, each capable of giving rise to all six follicular epithelial fates. Moreover, analysis of mosaic pelage, as well as cultured whisker follicles provided evidence that bulb-associated progenitors can give rise to expanding descendant clones during midanagen, leading to the conclusion that the bulb contains dormant or symmetrically dividing stem cells. This latter feature resembles the behavior of hematopoietic stem cells after bone marrow transplantation, and raises the question of whether this property may be shared by stem cells in other self-renewing epithelia.
KW - Epithelial differentiation
KW - Genetic mosaic mouse models
KW - Hair follicle
KW - Stem cells
UR - http://www.scopus.com/inward/record.url?scp=18244385529&partnerID=8YFLogxK
U2 - 10.1006/dbio.2001.0516
DO - 10.1006/dbio.2001.0516
M3 - Article
C2 - 11795939
AN - SCOPUS:18244385529
SN - 0012-1606
VL - 242
SP - 44
EP - 57
JO - Developmental Biology
JF - Developmental Biology
IS - 1
ER -