Evidence map›Paper›PMID 33566676›Full record

ArticleMolecular biology of the cell2021

Spatial regulation of MCAK promotes cell polarization and focal adhesion turnover to drive robust cell migration.

Hailing Zong, Mark Hazelbaker, Christina Moe, Stephanie C Ems-McClung, Ke Hu, Claire E Walczak

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
1.5field-weighted citation impact, top 20% of its field
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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Decoding Rho GTPase signalling networks in directed cell migration.Frontiers in cell and developmental biology · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Microtubule detyrosination drives symmetry breaking to polarize cells for directed cell migration.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Article
  11. Article
  12. Article
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 at 1 institution in 1 country.

Hailing ZongDepartment of Biology, Indiana University, Bloomington, IN 47405.
Mark HazelbakerMedical Sciences, Indiana University School of Medicine-Bloomington, Bloomington, IN 47405.
Christina MoeDepartment of Biology, Indiana University, Bloomington, IN 47405.
Stephanie C Ems-McClungMedical Sciences, Indiana University School of Medicine-Bloomington, Bloomington, IN 47405.
Ke HuDepartment of Biology, Indiana University, Bloomington, IN 47405.
Claire E WalczakMedical Sciences, Indiana University School of Medicine-Bloomington, Bloomington, IN 47405.
Indiana University Bloomington · US

Funding

Mechanisms of Mitotic FidelityR35GM122482 · NIGMS · INDIANA UNIVERSITY INDIANAPOLIS · PI Claire E Walczak · 2017 to 2026
$4.4M
NIGMS NIH HHS R35 GM122482
6 · The paper itself

Abstract

The asymmetric distribution of microtubule (MT) dynamics in migrating cells is important for cell polarization, yet the underlying regulatory mechanisms remain underexplored. Here, we addressed this question by studying the role of the MT depolymerase, MCAK (mitotic centromere-associated kinesin), in the highly persistent migration of RPE-1 cells. MCAK knockdown leads to slowed migration and poor directional movement. Fixed and live cell imaging revealed that MCAK knockdown results in excessive membrane ruffling as well as defects in cell polarization and the maintenance of a major protrusive front. Additionally, loss of MCAK increases the lifetime of focal adhesions by decreasing their disassembly rate. These functions correlate with a spatial distribution of MCAK activity, wherein activity is higher in the trailing edge of cells compared with the leading edge. Overexpression of Rac1 has a dominant effect over MCAK activity, placing it downstream of or in a parallel pathway to MCAK function in migration. Together, our data support a model in which the polarized distribution of MCAK activity and subsequent differential regulation of MT dynamics contribute to cell polarity, centrosome positioning, and focal adhesion dynamics, which all help facilitate robust directional migration.

Indexed as

Cell AdhesionCell MovementCell PolarityCentromereFocal AdhesionsHumansKinesinsMicrotubulesMitosisPhosphorylationProtein Serine-Threonine KinasesKIF2C protein, humanKinesinsProtein Serine-Threonine Kinases

Identifiers

PMID33566676
PMCPMC8101467
OpenAlexW3127916154

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

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.