Literature DB >> 21185581

Podoplanin is expressed by a sub-population of human foetal rib and knee joint rudiment chondrocytes.

Susan M Smith1, James Melrose.   

Abstract

The aim of this study was to determine if podoplanin was expressed by rudiment chondrocytes in human foetal cartilages. Podoplanin was immunolocalised in first trimester human foetal rib and knee joint rudiments to a sub-population of chondrocytes deep in the rib rudiments, tibial and femoral growth plates and cells associated with the cartilage canals of the foetal knee joint rudiments. Lymphatic vessels in the loose stromal tissues surrounding the developing rudiments were also demonstrated on the same histology slides using antipodoplanin (MAb D2-40) and anti-LYVE-1 and differentiated from CD-31 positive blood vessels confirming the discriminative capability of the antibody preparations used. The D2-40 positive rib and knee rudiment chondrocytes were not stained with antibodies to LYVE-1, CD-31 or CD-34 however perlecan was a prominent pericellular proteoglycan around these cells confirming their chondrogenic phenotype. Discernable differences were evident between the surface and deep rudiment chondrocytes in terms of their antigen reactivities detected with MAb D2-40 or antiperlecan antibodies. Binding of the cytoplasmic tail of PDPN to the ERM proteins ezrin, radixin and moeisin may result in changes in cytoskeletal organisation which alter the phenotype of this central population of rudiment cells. This may contribute to morphological changes in the rudiment cartilages which lead to establishment of the primary ossification centres and is consistent with their roles as transient developmental scaffolds during tissue development.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 21185581     DOI: 10.1016/j.tice.2010.11.003

Source DB:  PubMed          Journal:  Tissue Cell        ISSN: 0040-8166            Impact factor:   2.466


  4 in total

1.  Distribution and alteration of lymphatic vessels in knee joints of normal and osteoarthritic mice.

Authors:  Jixiang Shi; Qianqian Liang; Michael Zuscik; Jie Shen; Di Chen; Hao Xu; Yong-Jun Wang; Yan Chen; Ronald W Wood; Jia Li; Brendan F Boyce; Lianping Xing
Journal:  Arthritis Rheumatol       Date:  2014-03       Impact factor: 10.995

2.  The brain-tumor related protein podoplanin regulates synaptic plasticity and hippocampus-dependent learning and memory.

Authors:  Ana Cicvaric; Jiaye Yang; Sigurd Krieger; Deeba Khan; Eun-Jung Kim; Manuel Dominguez-Rodriguez; Maureen Cabatic; Barbara Molz; Juan Pablo Acevedo Aguilar; Radoslav Milicevic; Tarik Smani; Johannes M Breuss; Dontscho Kerjaschki; Daniela D Pollak; Pavel Uhrin; Francisco J Monje
Journal:  Ann Med       Date:  2016-08-25       Impact factor: 4.709

3.  Podoplanin Gene Disruption in Mice Promotes in vivo Neural Progenitor Cells Proliferation, Selectively Impairs Dentate Gyrus Synaptic Depression and Induces Anxiety-Like Behaviors.

Authors:  Ana Cicvaric; Hannah M Sachernegg; Tamara Stojanovic; Dörte Symmank; Tarik Smani; Thomas Moeslinger; Pavel Uhrin; Francisco J Monje
Journal:  Front Cell Neurosci       Date:  2020-01-15       Impact factor: 5.505

4.  Podoplanin is an important stromal prognostic marker in perihilar cholangiocarcinoma.

Authors:  Halmurat Obulkasim; Xiaolei Shi; Jun Wang; Jun Li; Bo Dai; Pengwen Wu; Shuai Wang; Xun Wang; Yitao Ding
Journal:  Oncol Lett       Date:  2017-11-02       Impact factor: 2.967

  4 in total

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