Abstract | CONTEXT: OBJECTIVE: We aimed to provide insight into the disease mechanism in GHS. METHODS: We studied a cohort of 6 multiplex families with GHS through autozygosity mapping and whole-exome sequencing. RESULTS: We identified 6 patients from 3 independent families carrying loss-of-function mutations in PNPLA6, which encodes neuropathy target esterase (NTE), a lysophospholipase that maintains intracellular phospholipid homeostasis by converting lysophosphatidylcholine to glycerophosphocholine. Wild-type PNPLA6, but not PNPLA6 bearing these mutations, rescued a well-established Drosophila neurodegenerative phenotype caused by the absence of sws, the fly ortholog of mammalian PNPLA6. Inhibition of NTE activity in the LβT2 gonadotrope cell line diminished LH response to GnRH by reducing GnRH-stimulated LH exocytosis, without affecting GnRH receptor signaling or LHβ synthesis. CONCLUSION: These results suggest that NTE-dependent alteration of phospholipid homeostasis in GHS causes both neurodegeneration and impaired LH release from pituitary gonadotropes, leading to nHH.
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Authors | A Kemal Topaloglu, Alejandro Lomniczi, Doris Kretzschmar, Gregory A Dissen, L Damla Kotan, Craig A McArdle, A Filiz Koc, Ben C Hamel, Metin Guclu, Esra D Papatya, Erdal Eren, Eda Mengen, Fatih Gurbuz, Mandy Cook, Juan M Castellano, M Burcu Kekil, Neslihan O Mungan, Bilgin Yuksel, Sergio R Ojeda |
Journal | The Journal of clinical endocrinology and metabolism
(J Clin Endocrinol Metab)
Vol. 99
Issue 10
Pg. E2067-75
(Oct 2014)
ISSN: 1945-7197 [Electronic] United States |
PMID | 25033069
(Publication Type: Case Reports, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
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Chemical References |
- Phospholipids
- Gonadotropin-Releasing Hormone
- PNPLA6 protein, human
- Phospholipases
- Carboxylic Ester Hydrolases
- neurotoxic esterase
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Topics |
- Adolescent
- Carboxylic Ester Hydrolases
(genetics, metabolism)
- Cerebellar Ataxia
(genetics, metabolism)
- Family Health
- Female
- Gonadotropin-Releasing Hormone
(deficiency, genetics, metabolism)
- Homeostasis
(genetics)
- Humans
- Hypogonadism
(genetics, metabolism)
- Male
- Middle Aged
- Nerve Degeneration
(genetics, metabolism)
- Pedigree
- Phospholipases
(genetics, metabolism)
- Phospholipids
(metabolism)
- Puberty, Delayed
(genetics, metabolism)
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