Literature DB >> 34453724

Use of Immunohistochemistry to Determine Expression of Rab5 Subfamily of GTPases in Mature and Developmental Brains.

Kwok-Ling Kam1, Paige Parrack1, Marcellus Banworth2, Sheeja Aravindan3, Guangpu Li4, Kar-Ming Fung5.   

Abstract

Rab GTPases are essentially molecular switches. They serve as master regulators in intracellular membrane trafficking from the formation and transport of vesicles at the originating organelle to its fusion to the membrane at the target organelle. Their functions are diversified and each has their specific subcellular location. Their expression may vary significantly in the same cell when the level of protein production is significantly different in different physiologic status. One of the best examples is the transition from fetal to mature status of cells. Expression and localization of Rab GTPases in mature and developing brains have not been well studied. Immunohistochemistry is an efficient way in the detection, semiquantitation, and localization of Rab GTPases in tissue sections. It is inexpensive and fast which allow efficient mass screening of many sections. In this chapter, we describe the immunohistochemical assay protocol for analyzing several Rab protein expressions of the Rab5 subfamily, including Rab5, Rab17, Rab22, and Rab31, in developmental (fetal) and mature human brains.
© 2021. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Brain; Fetal brain; GTPase; Neurodevelopment; Rab17; Rab22; Rab31; Rab5

Mesh:

Substances:

Year:  2021        PMID: 34453724      PMCID: PMC8917831          DOI: 10.1007/978-1-0716-1346-7_19

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  27 in total

1.  Rab22a regulates the recycling of membrane proteins internalized independently of clathrin.

Authors:  Roberto Weigert; Albert Chi Yeung; Jean Li; Julie G Donaldson
Journal:  Mol Biol Cell       Date:  2004-06-04       Impact factor: 4.138

2.  Phosphorylation negatively regulates exosome mediated secretion of cryAB in glioma cells.

Authors:  Rajshekhar A Kore; Edathara C Abraham
Journal:  Biochim Biophys Acta       Date:  2015-11-24

3.  rab5 controls early endosome fusion in vitro.

Authors:  J P Gorvel; P Chavrier; M Zerial; J Gruenberg
Journal:  Cell       Date:  1991-03-08       Impact factor: 41.582

4.  A role for the small GTPase Rab21 in the early endocytic pathway.

Authors:  Jeremy C Simpson; Gareth Griffiths; Marianne Wessling-Resnick; Jack A M Fransen; Holly Bennett; Arwyn T Jones
Journal:  J Cell Sci       Date:  2004-11-23       Impact factor: 5.285

5.  Rab3a promotes brain tumor initiation and progression.

Authors:  Jun-Kyum Kim; Seung-Yup Lee; Chang-Won Park; Suk-Hwang Park; Jinlong Yin; Jaebong Kim; Jae-Bong Park; Jae-Yong Lee; Hyunggee Kim; Sung-Chan Kim
Journal:  Mol Biol Rep       Date:  2014-06-26       Impact factor: 2.316

6.  Transport of mannose-6-phosphate receptors from the trans-Golgi network to endosomes requires Rab31.

Authors:  A G Rodriguez-Gabin; X Yin; Q Si; J N Larocca
Journal:  Exp Cell Res       Date:  2009-04-05       Impact factor: 3.905

Review 7.  Regulation of membrane traffic by Rab GEF and GAP cascades.

Authors:  Peter Novick
Journal:  Small GTPases       Date:  2016-07-18

Review 8.  Critical importance of RAB proteins for synaptic function.

Authors:  Maria Lidia Mignogna; Patrizia D'Adamo
Journal:  Small GTPases       Date:  2017-04-13

9.  Untangling the evolution of Rab G proteins: implications of a comprehensive genomic analysis.

Authors:  Tobias H Klöpper; Nickias Kienle; Dirk Fasshauer; Sean Munro
Journal:  BMC Biol       Date:  2012-08-08       Impact factor: 7.431

10.  Cooperative interaction between the MUC1-C oncoprotein and the Rab31 GTPase in estrogen receptor-positive breast cancer cells.

Authors:  Caining Jin; Hasan Rajabi; Sean Pitroda; Ailing Li; Akriti Kharbanda; Ralph Weichselbaum; Donald Kufe
Journal:  PLoS One       Date:  2012-07-09       Impact factor: 3.240

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