6533b7d5fe1ef96bd1263c78

RESEARCH PRODUCT

An O2-sensitive glomus cell-stem cell synapse induces carotid body growth in chronic hypoxia.

José López-barneoRicardo PardalRocío DuránAida Platero-luengoBlanca Diaz-castroJosé I. PiruatJosé Manuel García-verdugoSusana González-granero

subject

medicine.medical_specialtyMice TransgenicBiologyGeneral Biochemistry Genetics and Molecular BiologyProlyl HydroxylasesMiceGlomus cellNeural Stem CellsInternal medicinemedicineAnimalsRats WistarCell ProliferationCarotid BodyCell growthBiochemistry Genetics and Molecular Biology(all)Germinal centerCell DifferentiationHypoxia (medical)Respiratory CenterNeural stem cellRatsOxygenEndocrinologymedicine.anatomical_structureCarotid bodyStem cellmedicine.symptomEndothelin receptor

description

Summary Neural stem cells (NSCs) exist in germinal centers of the adult brain and in the carotid body (CB), an oxygen-sensing organ that grows under chronic hypoxemia. How stem cell lineage differentiation into mature glomus cells is coupled with changes in physiological demand is poorly understood. Here, we show that hypoxia does not affect CB NSC proliferation directly. Rather, mature glomus cells expressing endothelin-1, the O 2 -sensing elements in the CB that secrete neurotransmitters in response to hypoxia, establish abundant synaptic-like contacts with stem cells, which express endothelin receptors, and instruct their growth. Inhibition of glomus cell transmitter release or their selective destruction markedly diminishes CB cell growth during hypoxia, showing that CB NSCs are under the direct "synaptic" control of the mature O 2 -sensitive cells. Thus, glomus cells not only acutely activate the respiratory center but also induce NSC-dependent CB hypertrophy necessary for acclimatization to chronic hypoxemia.

10.1016/j.cell.2013.12.013https://pubmed.ncbi.nlm.nih.gov/24439383