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Abnormal B-cell development in TIMP-deficient bone marrow.
Weiss, Ashley; Saw, Sanjay; Aiken, Alison; Aliar, Kazeera; Shao, Yang W; Fang, Hui; Narala, Swami; Shetty, Ronak; Waterhouse, Paul D; Khokha, Rama.
Affiliation
  • Weiss A; Princess Margaret Cancer Centre/University Health Network, Toronto, ON, Canada.
  • Saw S; Department of Laboratory Medicine and Pathobiology; and.
  • Aiken A; Princess Margaret Cancer Centre/University Health Network, Toronto, ON, Canada.
  • Aliar K; Princess Margaret Cancer Centre/University Health Network, Toronto, ON, Canada.
  • Shao YW; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
  • Fang H; Princess Margaret Cancer Centre/University Health Network, Toronto, ON, Canada.
  • Narala S; Princess Margaret Cancer Centre/University Health Network, Toronto, ON, Canada.
  • Shetty R; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
  • Waterhouse PD; Princess Margaret Cancer Centre/University Health Network, Toronto, ON, Canada.
  • Khokha R; Princess Margaret Cancer Centre/University Health Network, Toronto, ON, Canada.
Blood Adv ; 5(20): 3960-3974, 2021 10 26.
Article in En | MEDLINE | ID: mdl-34500457
Bone marrow (BM) is the primary site of hematopoiesis and is responsible for a lifelong supply of all blood cell lineages. The process of hematopoiesis follows key intrinsic programs that also integrate instructive signals from the BM niche. First identified as an erythropoietin-potentiating factor, the tissue inhibitor of metalloproteinase (TIMP) protein family has expanded to 4 members and has widely come to be viewed as a classical regulator of tissue homeostasis. By virtue of metalloprotease inhibition, TIMPs not only regulate extracellular matrix turnover but also control growth factor bioavailability. The 4 mammalian TIMPs possess overlapping enzyme-inhibition profiles and have never been studied for their cumulative role in hematopoiesis. Here, we show that TIMPs are critical for postnatal B lymphopoiesis in the BM. TIMP-deficient mice have defective B-cell development arising at the pro-B-cell stage. Expression analysis of TIMPless hematopoietic cell subsets pointed to an altered B-cell program in the Lineage-Sca-1+c-Kit+ (LSK) cell fraction. Serial and competitive BM transplants identified a defect in TIMP-deficient hematopoietic stem and progenitor cells for B lymphopoiesis. In parallel, reverse BM transplants uncovered the extrinsic role of stromal TIMPs in pro- and pre-B-cell development. TIMP deficiency disrupted CXCL12 localization to LepR+ cells, and increased soluble CXCL12 within the BM niche. It also compromised the number and morphology of LepR+ cells. These data provide new evidence that TIMPs control the cellular and biochemical makeup of the BM niche and influence the LSK transcriptional program required for optimal B lymphopoiesis.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Marrow / Bone Marrow Cells Type of study: Prognostic_studies Limits: Animals Language: En Journal: Blood Adv Year: 2021 Document type: Article Affiliation country: Canada Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Marrow / Bone Marrow Cells Type of study: Prognostic_studies Limits: Animals Language: En Journal: Blood Adv Year: 2021 Document type: Article Affiliation country: Canada Country of publication: United States