Single-cell expression profiling of human epidermal stem and transit-amplifying cells: Lrig1 is a regulator of stem cell quiescence

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Single-cell expression profiling of human epidermal stem and transit-amplifying cells : Lrig1 is a regulator of stem cell quiescence. / Jensen, Kim B; Watt, Fiona M.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 103, No. 32, 08.08.2006, p. 11958-63.

Research output: Contribution to journalJournal articleResearch

Harvard

Jensen, KB & Watt, FM 2006, 'Single-cell expression profiling of human epidermal stem and transit-amplifying cells: Lrig1 is a regulator of stem cell quiescence', Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 32, pp. 11958-63. https://doi.org/10.1073/pnas.0601886103

APA

Jensen, K. B., & Watt, F. M. (2006). Single-cell expression profiling of human epidermal stem and transit-amplifying cells: Lrig1 is a regulator of stem cell quiescence. Proceedings of the National Academy of Sciences of the United States of America, 103(32), 11958-63. https://doi.org/10.1073/pnas.0601886103

Vancouver

Jensen KB, Watt FM. Single-cell expression profiling of human epidermal stem and transit-amplifying cells: Lrig1 is a regulator of stem cell quiescence. Proceedings of the National Academy of Sciences of the United States of America. 2006 Aug 8;103(32):11958-63. https://doi.org/10.1073/pnas.0601886103

Author

Jensen, Kim B ; Watt, Fiona M. / Single-cell expression profiling of human epidermal stem and transit-amplifying cells : Lrig1 is a regulator of stem cell quiescence. In: Proceedings of the National Academy of Sciences of the United States of America. 2006 ; Vol. 103, No. 32. pp. 11958-63.

Bibtex

@article{98125cc9dd0d4a26a08adaa83c50feaa,
title = "Single-cell expression profiling of human epidermal stem and transit-amplifying cells: Lrig1 is a regulator of stem cell quiescence",
abstract = "Considerable progress has been made in characterizing epidermal stem cells by microarray analysis of FACS-selected populations. One limitation of this approach is that the gene expression profiles represent the average of the cell population, potentially masking cellular heterogeneity of functional significance. To overcome this problem, we have performed single-cell expression profiling. We have generated cDNA libraries from single human epidermal cells, designated as stem or transit-amplifying cells on the basis of Delta1 and melanoma-associated chondroitin sulfate proteoglycan expression. Of the 14 putative stem cell markers identified, we selected one, the EGF receptor antagonist leucine-rich repeats and immunoglobulin-like domains 1 (Lrig1), for further study. Lrig1 was expressed in groups of basal cells in human interfollicular epidermis previously identified as enriched for stem cells. Overexpression of Lrig1 decreased keratinocyte proliferation but did not affect the proportion of stem and transit-amplifying cells, as judged by clonal growth characteristics. Down-regulation of Lrig1 using siRNA increased cell-surface EGF receptor levels, enhanced activation of downstream pathways, and stimulated proliferation. Lrig1 acted in part by negatively regulating the Myc promoter. We propose that Lrig1 maintains epidermal stem cells in a quiescent nondividing state, and that Lrig1 down-regulation triggers proliferation.",
keywords = "Biological Transport, Cell Adhesion, Cell Proliferation, Cell Separation, Down-Regulation, Epidermis, Flow Cytometry, Gene Expression Profiling, Gene Library, Humans, Keratinocytes, Membrane Glycoproteins, Promoter Regions, Genetic, Stem Cells",
author = "Jensen, {Kim B} and Watt, {Fiona M}",
year = "2006",
month = aug,
day = "8",
doi = "10.1073/pnas.0601886103",
language = "English",
volume = "103",
pages = "11958--63",
journal = "Proceedings of the National Academy of Sciences of the United States of America",
issn = "0027-8424",
publisher = "The National Academy of Sciences of the United States of America",
number = "32",

}

RIS

TY - JOUR

T1 - Single-cell expression profiling of human epidermal stem and transit-amplifying cells

T2 - Lrig1 is a regulator of stem cell quiescence

AU - Jensen, Kim B

AU - Watt, Fiona M

PY - 2006/8/8

Y1 - 2006/8/8

N2 - Considerable progress has been made in characterizing epidermal stem cells by microarray analysis of FACS-selected populations. One limitation of this approach is that the gene expression profiles represent the average of the cell population, potentially masking cellular heterogeneity of functional significance. To overcome this problem, we have performed single-cell expression profiling. We have generated cDNA libraries from single human epidermal cells, designated as stem or transit-amplifying cells on the basis of Delta1 and melanoma-associated chondroitin sulfate proteoglycan expression. Of the 14 putative stem cell markers identified, we selected one, the EGF receptor antagonist leucine-rich repeats and immunoglobulin-like domains 1 (Lrig1), for further study. Lrig1 was expressed in groups of basal cells in human interfollicular epidermis previously identified as enriched for stem cells. Overexpression of Lrig1 decreased keratinocyte proliferation but did not affect the proportion of stem and transit-amplifying cells, as judged by clonal growth characteristics. Down-regulation of Lrig1 using siRNA increased cell-surface EGF receptor levels, enhanced activation of downstream pathways, and stimulated proliferation. Lrig1 acted in part by negatively regulating the Myc promoter. We propose that Lrig1 maintains epidermal stem cells in a quiescent nondividing state, and that Lrig1 down-regulation triggers proliferation.

AB - Considerable progress has been made in characterizing epidermal stem cells by microarray analysis of FACS-selected populations. One limitation of this approach is that the gene expression profiles represent the average of the cell population, potentially masking cellular heterogeneity of functional significance. To overcome this problem, we have performed single-cell expression profiling. We have generated cDNA libraries from single human epidermal cells, designated as stem or transit-amplifying cells on the basis of Delta1 and melanoma-associated chondroitin sulfate proteoglycan expression. Of the 14 putative stem cell markers identified, we selected one, the EGF receptor antagonist leucine-rich repeats and immunoglobulin-like domains 1 (Lrig1), for further study. Lrig1 was expressed in groups of basal cells in human interfollicular epidermis previously identified as enriched for stem cells. Overexpression of Lrig1 decreased keratinocyte proliferation but did not affect the proportion of stem and transit-amplifying cells, as judged by clonal growth characteristics. Down-regulation of Lrig1 using siRNA increased cell-surface EGF receptor levels, enhanced activation of downstream pathways, and stimulated proliferation. Lrig1 acted in part by negatively regulating the Myc promoter. We propose that Lrig1 maintains epidermal stem cells in a quiescent nondividing state, and that Lrig1 down-regulation triggers proliferation.

KW - Biological Transport

KW - Cell Adhesion

KW - Cell Proliferation

KW - Cell Separation

KW - Down-Regulation

KW - Epidermis

KW - Flow Cytometry

KW - Gene Expression Profiling

KW - Gene Library

KW - Humans

KW - Keratinocytes

KW - Membrane Glycoproteins

KW - Promoter Regions, Genetic

KW - Stem Cells

U2 - 10.1073/pnas.0601886103

DO - 10.1073/pnas.0601886103

M3 - Journal article

C2 - 16877544

VL - 103

SP - 11958

EP - 11963

JO - Proceedings of the National Academy of Sciences of the United States of America

JF - Proceedings of the National Academy of Sciences of the United States of America

SN - 0027-8424

IS - 32

ER -

ID: 94415321