Evidence map›Paper›PMID 41827867›Full record

ArticleCells2026

LRP1 in Adult-Born Neural Stem Cells Modulates Neurogenesis and Hippocampal Memory.

Kristi Dietert, Nicole Marion, Meng Wang, Pamela Reed, Erzsebet Kokovay, Naomi L Sayre

Abstract read
In one paragraph

Article in Cells, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Kristi DietertDepartment of Neurosurgery, University of Texas Health Science Center, San Antonio, TX 78229, USA.ORCID 0000-0003-2338-7968
Nicole MarionDepartment of Neurosurgery, University of Texas Health Science Center, San Antonio, TX 78229, USA.ORCID 0009-0000-6584-9564
Meng WangDepartment of Neurosurgery, University of Texas Health Science Center, San Antonio, TX 78229, USA.ORCID 0000-0002-3798-6091
Pamela ReedDepartment of Neurosurgery, University of Texas Health Science Center, San Antonio, TX 78229, USA.
Erzsebet KokovayDepartment of Neurosurgery, University of Texas Health Science Center, San Antonio, TX 78229, USA.
Naomi L SayreDepartment of Neurosurgery, University of Texas Health Science Center, San Antonio, TX 78229, USA.

Funding

South Texas Medical Scientist Training Program (STX-MSTP)T32GM145432 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Jose E Cavazos, Ratna K Vadlamudi · 2023 to 2026
$2.3M
NRSA Training Core (TL1)TL1TR002647 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CHUN, YONG-HEE PATRICIA, FREI, CHRISTOPHER R. · 2018 to 2022
$1.8M
LRP1 as a novel regulator of CXCR4 in adult neural stem cells and post-stroke responseR01NS132778 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Naomi Ledene Sayre · 2023 to 2026
$1.8M
Integrated Graduate Training Program in Neuroscience, UTHSCSAT32NS082145 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI David A Morilak · 2013 to 2026
$1.5M
South Texas Medical Scientist Training Program (STX-MSTP)T32GM113896 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CAVAZOS, JOSE E · 2018 to 2022
$1.1M
South Texas Alzheimer’s and Neurodegenerative Disorders Training ProgramT32AG082661 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Jose E Cavazos, PETER Thornton FOX · 2023 to 2026
$676k
American Heart Association 916018NCATS NIH HHS TL1TR002647NCI NIH HHS P30CA54174NIA NIH HHS T32 AG082661NIA NIH HHS T32AG082661NIGMS NIH HHS T32GM113896NIGMS NIH HHS T32GM145432NINDS NIH HHS R01 NS132778NINDS NIH HHS R01NS132778NINDS NIH HHS T32NS082145Veterans Administration 1K2BX003240
6 · The paper itself

Abstract

(1) Background: Adult neurogenesis within the hippocampus modulates hippocampal memory and is often dysregulated in diseases that cause memory dysfunction, notably Alzheimer's disease. We have discovered a novel modulator of hippocampal neurogenesis-low-density lipoprotein receptor-related protein 1 (LRP1). (2) Methods: Using an inducible knockout of LRP1, male and female mice were subject to loss of LRP1, specifically in adult-born neural stem cells at 3 months of age. (3) Results: After 6 months with the knockout, animals without LRP1 in adult-born neural stem cells displayed behavioral phenotypes consistent with deficits in working memory and hippocampal-mediated spatial memory. We also found that over time, increasing numbers of adult-born LRP1-knockout neurons were present, although those neurons were morphologically less complex with fewer dendrites than controls. Our data suggest that the increase in the total number of adult-born neurons 6 months after knockout is due to a subtle increase in hippocampal proliferation over time. (4) Conclusions: Altogether, our data suggest that LRP1 is an important and previously unknown regulator of hippocampal neurogenesis.

Indexed as

HippocampusLow Density Lipoprotein Receptor-Related Protein-1MemoryNeural Stem CellsNeurogenesisReceptors, LDLTumor Suppressor ProteinsAnimalsCell ProliferationFemaleMaleMiceMice, KnockoutNeuronsLow Density Lipoprotein Receptor-Related Protein-1Lrp1 protein, mouseReceptors, LDLTumor Suppressor Proteinsadult neurogenesiscell deathhippocampal neurogenesislipoprotein receptorLRP1memory dysfunctionproliferationsubgranular zone

Identifiers

PMID41827867
PMCPMC12984419

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.