MKL1 deficiency results in a severe neutrophil motility defect due to impaired actin polymerization

Blood. 2020 Jun 11;135(24):2171-2181. doi: 10.1182/blood.2019002633.

Abstract

Megakaryoblastic leukemia 1 (MKL1) promotes the regulation of essential cell processes, including actin cytoskeletal dynamics, by coactivating serum response factor. Recently, the first human with MKL1 deficiency, leading to a novel primary immunodeficiency, was identified. We report a second family with 2 siblings with a homozygous frameshift mutation in MKL1. The index case died as an infant from progressive and severe pneumonia caused by Pseudomonas aeruginosa and poor wound healing. The younger sibling was preemptively transplanted shortly after birth. The immunodeficiency was marked by a pronounced actin polymerization defect and a strongly reduced motility and chemotactic response by MKL1-deficient neutrophils. In addition to the lack of MKL1, subsequent proteomic and transcriptomic analyses of patient neutrophils revealed actin and several actin-related proteins to be downregulated, confirming a role for MKL1 as a transcriptional coregulator. Degranulation was enhanced upon suboptimal neutrophil activation, whereas production of reactive oxygen species was normal. Neutrophil adhesion was intact but without proper spreading. The latter could explain the observed failure in firm adherence and transendothelial migration under flow conditions. No apparent defect in phagocytosis or bacterial killing was found. Also, monocyte-derived macrophages showed intact phagocytosis, and lymphocyte counts and proliferative capacity were normal. Nonhematopoietic primary fibroblasts demonstrated defective differentiation into myofibroblasts but normal migration and F-actin content, most likely as a result of compensatory mechanisms of MKL2, which is not expressed in neutrophils. Our findings extend current insight into the severe immune dysfunction in MKL1 deficiency, with cytoskeletal dysfunction and defective extravasation of neutrophils as the most prominent features.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / chemistry
  • Actin Cytoskeleton / metabolism*
  • Cell Movement / genetics
  • Cell Movement / physiology
  • Consanguinity
  • Female
  • Fibroblasts / metabolism
  • Frameshift Mutation*
  • Gene Expression Profiling
  • Hematopoietic Stem Cell Transplantation
  • Humans
  • Infant
  • Male
  • Neutrophils / physiology*
  • Pedigree
  • Polymerization
  • Primary Immunodeficiency Diseases / genetics*
  • Primary Immunodeficiency Diseases / metabolism*
  • Primary Immunodeficiency Diseases / therapy
  • Proteomics
  • Trans-Activators / deficiency*
  • Trans-Activators / genetics*
  • Transcription Factors / metabolism

Substances

  • MRTFA protein, human
  • MRTFB protein, human
  • Trans-Activators
  • Transcription Factors