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Multiple isoforms of the tumor protein p73 are expressed in the adult human telencephalon and choroid plexus and present in the cerebrospinal fluid
Author(s) -
CabreraSocorro Alfredo,
Morlans Mercedes Pueyo,
Sola Maria Luisa Suarez,
Delgado Francisco J. Gonzalez,
CastañeyraPerdomo Agustin,
Marin Maria C.,
Meyer Gundela
Publication year - 2006
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/j.1460-9568.2006.04750.x
Subject(s) - choroid plexus , subcommissural organ , cerebrum , cerebrospinal fluid , biology , gene isoform , immunohistochemistry , hippocampus , pathology , ependymal cell , microbiology and biotechnology , central nervous system , endocrinology , neuroscience , medicine , immunology , gene , biochemistry
Abstract p73, a homolog of the p53 tumor suppressor, codes for full‐length transactivating (TA) and N‐terminally truncated (ΔN) isoforms, with pro‐ and anti‐apoptotic activities, respectively. We examined the expression of the main p73 isoforms in adult human and mouse telencephalon and choroid plexus by immunohistochemistry on paraffin sections, and immunoblotting (IB) of tissue extracts and cerebrospinal fluid (CSF), using antibodies against different protein domains. Cortical neurons expressed TAp73 predominantly in the cytoplasm and ΔNp73 mainly in the nucleus, with partial overlap in the cytoplasm. Highest expression was found in the hippocampus. IB showed an array of TAp73 variants in adult human cortex and hippocampus. IB of human choroid plexus and CSF using TAp73‐specific antibodies revealed the presence of a ∼90‐kDa protein whose molecular weight was reduced after N‐deglycosylation, suggesting that glycosylated TAp73 is exported into the CSF. In the mouse, high expression of TAp73 was also detected in the subcommissural organ (SCO), an ependymal gland absent in adult humans. TAp73 colocalized with anti‐fibra‐Reissner‐antibody (AFRU), which is a marker of Reissner's fiber, the secreted SCO product. p73‐deficient mice had generalized cortical hypoplasia and hydrocephalus; in addition, we observed a dramatic size reduction of the choroid plexus. However, the SCOs were apparently unaltered and continued to secrete Reissner's fiber. Our findings point to complex and widespread p73 activities in the maintenance of adult cortical neurons and in brain homeostasis. TAp73 in the CSF may play important roles in the maintenance of the adult ventricular wall as well as in the development of the proliferating neuroepithelium.