Literature DB >> 32378740

Presynaptic dysfunction in neurodevelopmental disorders: Insights from the synaptic vesicle life cycle.

Katherine Bonnycastle1,2,3, Elizabeth C Davenport1,2,3, Michael A Cousin1,2,3.   

Abstract

The activity-dependent fusion, retrieval and recycling of synaptic vesicles is essential for the maintenance of neurotransmission. Until relatively recently it was believed that most mutations in genes that were essential for this process would be incompatible with life, because of this fundamental role. However, an ever-expanding number of mutations in this very cohort of genes are being identified in individuals with neurodevelopmental disorders, including autism, intellectual disability and epilepsy. This article will summarize the current state of knowledge linking mutations in presynaptic genes to neurodevelopmental disorders by sequentially covering the various stages of the synaptic vesicle life cycle. It will also discuss how perturbations of specific stages within this recycling process could translate into human disease. Finally, it will also provide perspectives on the potential for future therapy that are targeted to presynaptic function.
© 2020 International Society for Neurochemistry.

Entities:  

Keywords:  autism; endocytosis; epilepsy; exocytosis; intellectual disability; neurotransmission; vesicle

Mesh:

Year:  2020        PMID: 32378740     DOI: 10.1111/jnc.15035

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.546


  13 in total

Review 1.  Vesicle trafficking with snares: a perspective for autism.

Authors:  Çilem Özdemir; Nilfer Şahin; Tuba Edgünlü
Journal:  Mol Biol Rep       Date:  2022-10-05       Impact factor: 2.742

2.  Presynaptic Rac1 controls synaptic strength through the regulation of synaptic vesicle priming.

Authors:  Christian Keine; Mohammed Al-Yaari; Tamara Radulovic; Connon I Thomas; Paula Valino Ramos; Debbie Guerrero-Given; Mrinalini Ranjan; Holger Taschenberger; Naomi Kamasawa; Samuel M Young
Journal:  Elife       Date:  2022-10-10       Impact factor: 8.713

Review 3.  Prenatal Zinc Deficient Mice as a Model for Autism Spectrum Disorders.

Authors:  Ann Katrin Sauer; Simone Hagmeyer; Andreas M Grabrucker
Journal:  Int J Mol Sci       Date:  2022-05-29       Impact factor: 6.208

4.  Temporal Vestibular Deficits in synaptojanin 1 (synj1) Mutants.

Authors:  Yan Gao; Teresa Nicolson
Journal:  Front Mol Neurosci       Date:  2021-01-18       Impact factor: 5.639

5.  Autism-associated synaptic vesicle transcripts are differentially expressed in maternal plasma exosomes of physiopathologic pregnancies.

Authors:  Yangwu Fang; Chan Wan; Youlu Wen; Ze Wu; Jing Pan; Mei Zhong; Nanbert Zhong
Journal:  J Transl Med       Date:  2021-04-15       Impact factor: 5.531

6.  Minibrain kinase and calcineurin coordinate activity-dependent bulk endocytosis through synaptojanin.

Authors:  Yi-Jheng Peng; Junhua Geng; Ying Wu; Cristian Pinales; Jennifer Langen; Yen-Ching Chang; Christopher Buser; Karen T Chang
Journal:  J Cell Biol       Date:  2021-10-01       Impact factor: 8.077

7.  Fine-tuning activity-dependent bulk endocytosis via kinases and phosphatases.

Authors:  Ira Milosevic; Michael A Cousin
Journal:  J Cell Biol       Date:  2021-11-19       Impact factor: 8.077

8.  Exposure to GABAA Receptor Antagonist Picrotoxin in Pregnant Mice Causes Autism-Like Behaviors and Aberrant Gene Expression in Offspring.

Authors:  Hiroko Kotajima-Murakami; Hideo Hagihara; Atsushi Sato; Yoko Hagino; Miho Tanaka; Yoshihisa Katoh; Yasumasa Nishito; Yukio Takamatsu; Shigeo Uchino; Tsuyoshi Miyakawa; Kazutaka Ikeda
Journal:  Front Psychiatry       Date:  2022-02-03       Impact factor: 4.157

Review 9.  Synaptic Vesicle Recycling and the Endolysosomal System: A Reappraisal of Form and Function.

Authors:  Daniela Ivanova; Michael A Cousin
Journal:  Front Synaptic Neurosci       Date:  2022-02-25

10.  Expanding the genotype and phenotype spectrum of SYT1-associated neurodevelopmental disorder.

Authors:  Holly Melland; Fabian Bumbak; Anna Kolesnik-Taylor; Elise Ng-Cordell; Abinayah John; Panayiotis Constantinou; Shelagh Joss; Martin Larsen; Christina Fagerberg; Lone Walentin Laulund; Jenny Thies; Frances Emslie; Marjolein Willemsen; Tjitske Kleefstra; Rolf Pfundt; Rebekah Barrick; Richard Chang; Lucy Loong; Majid Alfadhel; Jasper van der Smagt; Mathilde Nizon; Manju A Kurian; Daniel J Scott; Joshua J Ziarek; Sarah L Gordon; Kate Baker
Journal:  Genet Med       Date:  2022-01-29       Impact factor: 8.864

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