Pathoconnectome Analysis of Müller Cells in Early Retinal Remodeling.
Pathoconnectome Analysis of Müller Cells in Early Retinal Remodeling.
复制标题
早期视网膜重塑中 Müller 细胞的病理连接组分析。
DOI:
10.1007/978-3-030-27378-1_60
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发表时间:
2019
影响因子:
--
通讯作者:
Jones,BryanW
中科院分区:
文献类型:
--
作者:
Pfeiffer,RebeccaL;Anderson,JamesR;Emrich,DanielP;Dahal,Jeebika;Sigulinsky,CrystalL;Morrison,HopeAB;Yang,Jia-Hui;Watt,CarlB;Rapp,KevinD;Kondo,Mineo;Terasaki,Hiroko;Garcia,JessicaC;Marc,RobertE;Jones,BryanW
Glia play important roles in neural function, including but not limited to amino acid recycling, ion homeostasis, glucose metabolism, and waste removal. During retinal degeneration and subsequent retinal remodeling, Müller cells (MCs) are the first cells to show metabolic and morphological alterations in response to stress. Metabolic alterations in MCs chaotically progress in retina undergoing photoreceptor degeneration; however, what relationship these alterations have with neuronal stress, synapse maintenance, or glia-glia interactions is currently unknown. The work described here reconstructs a MC from a pathoconnectome of early retinal remodeling retinal pathoconnectome 1 (RPC1) and explores relationships between MC structural and metabolic phenotypes in the context of neighboring neurons and glia. Here we find variations in intensity of osmication inter- and intracellularly, variation in small molecule metabolic content of MCs, as well as morphological alterations of glial endfeet. RPC1 provides a framework to analyze these relationships in early retinal remodeling through ultrastructural reconstructions of both neurons and glia. These reconstructions, informed by quantitative metabolite labeling via computational molecular phenotyping (CMP), allow us to evaluate neural-glial interactions in early retinal degeneration with unprecedented resolution and sensitivity.
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影响因子:
2.2
作者:
James R. Anderson;B. Jones;C. Watt;M. V. Shaw;Jia-Hui Yang;D. DeMill;J. S. Lauritzen;Yanhua Lin;K. Rapp;D. Mastronarde;Pavel A. Koshevoy;B. Grimm;T. Tasdizen;R. Whitaker;R. Marc
通讯作者:
James R. Anderson;B. Jones;C. Watt;M. V. Shaw;Jia-Hui Yang;D. DeMill;J. S. Lauritzen;Yanhua Lin;K. Rapp;D. Mastronarde;Pavel A. Koshevoy;B. Grimm;T. Tasdizen;R. Whitaker;R. Marc
影响因子:
4.2
作者:
Fariss, RN;Li, ZY;Milam, AH
通讯作者:
Milam, AH
DOI:
--
发表时间:
1998
期刊:
Investigative ophthalmology & visual science.
影响因子:
--
作者:
Marc,RE;Murry,RF;Fisher,SK;Linberg,KA;Lewis,GP
通讯作者:
Lewis,GP
影响因子:
3.4
作者:
Jones, B. W.;Pfeiffer, R. L.;Ferrell, W. D.;Watt, C. B.;Marmor, M.;Marc, R. E.
通讯作者:
Marc, R. E.
影响因子:
3.4
作者:
Pfeiffer, Rebecca L.;Marc, Robert E.;Kondo, Mineo;Terasaki, Hiroko;Jones, Bryan W.
通讯作者:
Jones, Bryan W.