Cited by 250Cell Adhesion Molecules ResearchNeuroscience and Neuropharmacology ResearchNeuroinflammation and Neurodegeneration Mechanisms

Integrin Subunit Gene Expression Is Regionally Differentiated in Adult Brain

Open access
Pinkstaff, Jason K., Detterich, Jon, Lynch, Gary, Gall, Christine·1999·The Journal of Neuroscience

Abstract

Integrins are a diverse family of heterodimeric (αβ) adhesion receptors recently shown to be concentrated within synapses and involved in the consolidation of long-term potentiation. Whether neuronal types or anatomical systems in the adult rat brain are coded by integrin type was studied in the present experiments by mapping the relative densities of mRNAs for nine α and four β subunits. Expression patterns were markedly different and in some regions complementary. General results and areas of notable labeling were as follows: α1—limited neuronal expression, neocortical layer V, hippocampal CA3; α3 and α5—diffuse neuronal and glial labeling, Purkinje cells, hippocampal stratum pyramidale, locus coeruleus (α3); α4— discrete limbic regions, olfactory cortical layer II, hippocampal CA2; α6—most prominently neuronal, neocortical subplate, endopiriform, subiculum; α7—discrete, all neocortical layers, hippocampal granule cells and CA3, cerebellar granule and Purkinje cells, all efferent cranial nerve nuclei; α8—discrete neuronal, deep cortex, hippocampal CA1, basolateral amygdala, striatum; αV—all cortical layers, striatum, Purkinje cells; β4—dentate gyrus granule cells; β5—broadly distributed, neocortex, medial amygdala, cerebellar granule and Purkinje cells, efferent cranial nerve nuclei; α2, β2, and β3—mRNAs not detected. These results establish that brain subfields express different balances of integrin subunits and thus different integrin receptors. Such variations will determine which matrix proteins are recognized by neurons and the types of intraneuronal signaling generated by matrix binding. They also could generate important differences in synaptic plasticity across brain systems.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1523/jneurosci.19-05-01541.1999

Cites

2 of 2 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • β1 integrins are the predominant integrin subunit in the central nervous system.

    “β1 integrins are the predominant integrin subunit in the central nervous system.”

    From The Serine/Threonine Kinase <scp>NDR2</scp> Regulates Integrin Signaling, Synapse Formation, and Synaptic Plasticity in the Hippocampus (2025) · cites this paper as Pinkstaff et al. 1999

    The Discussion (page unavailable) says that all α subunits studied can associate with β1, supporting a broad role for β1-containing integrins in adult brain. It does not establish that β1 is the predominant integrin subunit by abundance across the central nervous system. (LLM, conf=0.78)

    Experimental — accuracy not yet measured
  • β1 integrins are developmentally upregulated.

    “They are developmentally upegulated (Pinkstaff et al. 1999; Ikeshima‐Kataoka et al. 2022; Milner and Campbell 2002)”

    From The Serine/Threonine Kinase <scp>NDR2</scp> Regulates Integrin Signaling, Synapse Formation, and Synaptic Plasticity in the Hippocampus (2025) · cites this paper as Pinkstaff et al. 1999

    The Discussion reports β1 integrin expression in adult brain, but does not compare expression across developmental stages. Searches for developmental upregulation and postnatal changes found no passage establishing that β1 integrins increase during development; page numbers were unavailable in our copy. (LLM, conf=0.72)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 2

  1. Peters A, Palay SL, Webster H (1976) The fine structure of the nervous system. In: The neurons and supporting cells. Philadelphia: Saunders.
  2. Swanson L (1992) Brain maps: structure of the rat brain. Amsterdam: Elsevier.

Cited by

Sorted by citations

Authors
Pinkstaff, J. K., Detterich, J., Lynch, G., & Gall, C.
Affiliations
University of California, Irvine (US)
Venue
The Journal of Neuroscience
Published
1999-03-01
Volume
19
Issue
5
Pages
1541-1556
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W2107012136
Cited by
250
References
2
Citations by year
2026: 2 · 2025: 4 · 2024: 5 · 2023: 1 · 2022: 6 · 2021: 4 · 2019: 2 · 2018: 4 · 2017: 3 · 2016: 10 · 2015: 3 · 2014: 7 · 2013: 14 · 2012: 12
FWCI
6.57
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01ns026748-10)
  • National Institute of Neurological Disorders and Stroke (NS-26748, NS 37799, R01NS037799)
Topics
  • Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Keywords
integrin subunits, alpha-integrin, beta-integrin, neocortex, hippocampus, cerebellum, Purkinje cells, locus coeruleus, amygdala, striatum, synapses, extracellular matrix binding, synaptic plasticity, long-term potentiation
MeSH terms
Animals, Autoradiography, Brain, Male, Organ Specificity, RNA, Messenger, Tissue Distribution, Gene Expression, Integrins, Rats, Sprague-Dawley, In Situ Hybridization, Rats

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review