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      Stem cell self-renewal specified by JAK-STAT activation in response to a support cell cue.

      Science (New York, N.Y.)
      Animals, Cell Differentiation, Cell Division, Cell Lineage, Cues, DNA-Binding Proteins, genetics, metabolism, Drosophila, cytology, embryology, physiology, Drosophila Proteins, Germ Cells, Glycoproteins, Janus Kinases, Ligands, Male, Mutation, Protein-Tyrosine Kinases, STAT Transcription Factors, Signal Transduction, Spermatocytes, Spermatogenesis, Stem Cells, Testis, Trans-Activators, Transcription Factors

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          Abstract

          Stem cells generate many differentiated, short-lived cell types, such as blood, skin, and sperm, throughout adult life. Stem cells maintain a long-term capacity to divide, producing daughter cells that either self-renew or initiate differentiation. Although the surrounding microenvironment or "niche" influences stem cell fate decisions, few signals that emanate from the niche to specify stem cell self-renewal have been identified. Here we demonstrate that the apical hub cells in the Drosophila testis act as a cellular niche that supports stem cell self-renewal. Hub cells express the ligand Unpaired (Upd), which activates the Janus kinase-signal transducer and activator of transcription (JAK-STAT) pathway in adjacent germ cells to specify self-renewal and continual maintenance of the germ line stem cell population.

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