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Lung Stem and Progenitor Cells in Tissue Homeostasis and Disease

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76 Citas (Scopus)

Resumen

The mammalian lung is a complex organ containing numerous putative stem/progenitor cell populations that contribute to region-specific tissue homeostasis and repair. In this review, we discuss recent advances in identifying and studying these cell populations in the context of lung homeostasis and disease. Genetically engineered mice now allow for lineage tracing of several lung stem and progenitor cell populations in vivo during different types of lung injury repair. Using specific sets of cell surface markers, these cells can also be isolated from murine and human lung and tested in 3D culture systems and in vivo transplant assays. The pathology of devastating lung diseases, including lung cancers, is likely in part due to dysregulation and dysfunction of lung stem cells. More precise characterization of stem cells with identification of new, unique markers; improvement in isolation and transplant techniques; and further development of functional assays will ultimately lead to new therapies for a host of human lung diseases. In particular, lung cancer biology may be greatly informed by findings in normal lung stem cell biology as evidence suggests that lung cancer is a disease that begins in, and may be driven by, neoplastic lung stem cells.

Idioma originalEnglish
Título de la publicación alojadaCurrent Topics in Developmental Biology
Páginas207-233
Número de páginas27
DOI
EstadoPublished - 2014

Serie de la publicación

NombreCurrent Topics in Developmental Biology
Volumen107
ISSN (versión impresa)0070-2153

Nota bibliográfica

Funding Information:
We thank members of our laboratory for their discussions and critical comments on the chapter. Work in our laboratory is supported by the Post-Doctoral Fellowship, PF-12-151-01-DMC, from the American Cancer Society (CMF), the Ikaria Advancing Newborn Medicine Grant (KTL), American Medical Association Foundation SEED Grant (KTL), 5 T32HD7466-15 (KTL), RO1 HL090136, U01 HL100402 RFA-HL-09-004, American Cancer Society Research Scholar Grant RSG-08-082-01-MGO, the V Foundation for Cancer Research, a Basil O’Conner March of Dimes Starter Award, and the Harvard Stem Cell Institute (CFK).

Financiación

We thank members of our laboratory for their discussions and critical comments on the chapter. Work in our laboratory is supported by the Post-Doctoral Fellowship, PF-12-151-01-DMC, from the American Cancer Society (CMF), the Ikaria Advancing Newborn Medicine Grant (KTL), American Medical Association Foundation SEED Grant (KTL), 5 T32HD7466-15 (KTL), RO1 HL090136, U01 HL100402 RFA-HL-09-004, American Cancer Society Research Scholar Grant RSG-08-082-01-MGO, the V Foundation for Cancer Research, a Basil O’Conner March of Dimes Starter Award, and the Harvard Stem Cell Institute (CFK).

FinanciadoresNúmero del financiador
Basil O’Conner March of Dimes
Ikaria Advancing Newborn Medicine
American Cancer Society
National Heart, Lung, and Blood Institute (NHLBI)R01HL090136
V Foundation for Cancer Research
American Medical Association Foundation5 T32HD7466-15, U01 HL100402 RFA-HL-09-004, RSG-08-082-01-MGO, RO1 HL090136
Harvard Stem Cell Institute
CancerFree KIDS
Centrum för Miljövetenskaplig Forskning, Umeå Universitet

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Developmental Biology
    • Cell Biology

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